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382 Resultado(s)

Ordenados por

Financiado por un miembro del IRDiRC = Miembro de una ERN =

Registos y biobancos

ALEMANIA

Niedersachsen
GÖTTINGEN

ESNEK - Rare paediatric neurological disease registry Germany
Universitätsmedizin Göttingen
Geschäftsstelle der ESNEK

ALEMANIA

Nordrhein-Westfalen
MÜNSTER

Brain-Net - brain tissue bank Munster (pediatric neuropathology)
Institut für Neuropathologie der Medizinischen Fakultät Münster
Institut für Neuropathologie

BELGICA

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Central Registry of Rare Diseases (CRRD)
Sciensano
Health Services Research - Rare Diseases

ESPAÑA

Andalucía
SEVILLA

Registro de enfermedades raras de Andalucía
Junta de Andalucía. Consejería de Salud y Bienestar Social
Dirección General de Calidad, Investigación y Gestión del Conocimiento

ESPAÑA

Aragón
ZARAGOZA

Registro de enfermedades raras de la Comunidad Autónoma de Aragón
Gobierno de Aragón. Departamento de Sanidad, Bienestar Social y Familia
Servicio de Evaluación y Acreditación Sanitaria

ESPAÑA

Baleares
PALMA DE MALLORCA

Registro Poblacional de Enfermedades Raras de la Comunidad Autónoma de las Illes Balears
Govern de les Illes Balears. Dirección General de Salud Pública y Consumo
Servicio de Epidemiología

ESPAÑA

Baleares
PALMA DE MALLORCA

Registro Poblacional de Enfermedades Raras de la Comunidad Autónoma de las Illes Balears
Govern de les Illes Balears. Dirección General de Salud Pública y Consumo
Dirección General de Salud Pública y Consumo

ESPAÑA

Cantabria
SANTANDER

Registro poblacional de enfermedades raras y anomalias congenitas de Cantabria
Gobierno de Cantabria. Consejería de Sanidad y Servicios Sociales
Servicio de Atención Sanitaria

ESPAÑA

Comunidad Valenciana
VALENCIA

SIER-CV: Sistema de Información de Enfermedades Raras de la Comunitat Valenciana
FISABIO - Salud Pública
Área de Enfermedades Raras

ESPAÑA

Extremadura
MÉRIDA

Registro de enfermedades raras de Extremadura
Junta de Extremadura. Servicio Extremeño de Salud
Subdirector de Epidemiología

ESPAÑA

Galicia
SANTIAGO DE COMPOSTELA

RERGA: Registro de enfermedades raras de Galicia
Servicio Gallego de Salud
Servicio de Análisis y Evaluación Asistencial

ESPAÑA

Madrid
MADRID

SIERMA: Sistema de información de enfermedades raras de Madrid
Comunidad de Madrid. Subdirección de Promoción y Prevención de la Salud
Subdirección de Promoción y Prevención de la Salud

ESPAÑA

Madrid
MADRID

ReeR: Registro Estatal de Enfermedades Raras
ISCIII - Instituto de Salud Carlos III
Instituto de Investigación de Enfermedades Raras

ESPAÑA

Murcia
MURCIA

SIERrm: Sistema de Información sobre enfermedades raras de la Región de Murcia
Región de Murcia. Consejería de Sanidad y Política Social
Servicio de Planificación y Financiación Sanitaria

ESPAÑA

Navarra
PAMPLONA

Registro poblacional de enfermedades raras de Navarra
Instituto de Salud Pública y Laboral de Navarra
Sección de Epidemiología de Enfermedades No Transmisibles

FRANCIA

ILE-DE-FRANCE
PARIS

French National Registry for Rare Diseases (BNDMR)
AP-HP Campus Picpus - Département WIND (Web Innovation Données)
Banque Nationale de Données Maladies Rares (BNDMR)

SUIZA

Suisse Alémanique
BERN

Swiss Rare Disease Registry
Institute of Social and Preventive Medicine (ISPM)

SUIZA

Suisse Alémanique
ZÜRICH

Swiss Rare Disease Registry
Universitäts - Kinderspital Zürich - Eleonorenstiftung
Abteilung für Stoffwechselkrankheiten

ALEMANIA

Baden-Württemberg
TÜBINGEN

ERN [RND] - ERN-RND Registry: The ERN-RND Rare Neurological Disease Registry
Institut für Medizinische Genetik und angewandte Genomik Tübingen
Institut für Medizinische Genetik und angewandte Genomik

ALEMANIA

Bayern
ERLANGEN

EEBB: European Epilepsy Brain Bank
Universitätsklinikum Erlangen - Kopfkliniken
Neuropathologisches Institut

ALEMANIA

Bayern
ERLANGEN

German epilepsy registry
Universitätsklinikum Erlangen - Kopfkliniken
Neuropathologisches Institut

ALEMANIA

Nordrhein-Westfalen
AACHEN

Brain-net - brain tissue bank Aachen
Universitätsklinikum Aachen
Institut für Neuropathologie

ALEMANIA

Nordrhein-Westfalen
BONN

Brain-Net - brain tissue bank Bonn (epilepsy, brain tumor)
Universitätsklinikum Bonn (AöR)
Hirntumor-Referenzzentrum der DGNN

AUSTRIA

SALZBURG
SALZBURG

ASCIS - The Austrian Spinal Cord Injury Study
Universitätsklinikum der Paracelsus Medizinischen Privatuniversität
Universitätsklinik für Orthopädie und Traumatologie

BELGICA

ANTWERPEN
ANTWERPEN

Collection of FRA12A carrier DNA samples
University of Antwerp - UA
Medical Genetics Unit

BELGICA

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Belgian Neuromuscular Diseases Registry (BNMDR)
Sciensano
Health Services Research - Rare Diseases

BELGICA

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

ENRAH: European alternating hemiplegia and rare epilepsies registry in childhood
Secretariat Brussels, Postbus 10009
European Network for Research on Alternating Hemiplegia

CANADA

Alberta
CALGARY

Canadian Neuromuscular Disease Registry
University of Calgary Health Science Centre
Department of Clinical Neurosciences

CHIPRE

Cyprus
NICOSIA

ESLOVENIA

SLOVENIA
LJUBLJANA

Human tissue biobank of Neuromuscular diseases (EuroBioBank partner)
University Medical Center Ljubljana
Institute of Anatomy

ESPAÑA

Cataluña
BARCELONA

NMD-ES: Registro Español de Enfermedades Neuromusculares
Hospital de la Santa Creu i Sant Pau
Servicio de Neurología

ESPAÑA

Cataluña
ESPLUGUES DE LLOBREGAT

Biobanco del Hospital Infantil Sant Joan de Déu para la investigación (BHISJDI)
Fundació Sant Joan de Déu - Institut de Recerca Sant Joan de Déu
Biobanco del Hospital Infantil Sant Joan de Déu para la investigación

ESPAÑA

Madrid
MADRID

REDAPED: Registro español de ataxias y paraparesias espásticas degenerativas
ISCIII - Instituto de Salud Carlos III
Instituto de Investigación de Enfermedades Raras

FRANCIA

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

Leukofrance database and biobank
Institution: Information not provided - FR

FRANCIA

GRAND-EST
ILLKIRCH-GRAFFENSTADEN

Financiado por un miembro del IRDiRCRaDiCo-GenIDA: International social network for data collection on the natural history of rare monogenic forms of intellectual disabilities
Institut de génétique et de biologie moléculaire et cellulaire - IGBMC
Département Médecine translationnelle et neurogénétique

FRANCIA

ILE-DE-FRANCE
GARCHES

French registry of neuromuscular diseases from reference centres
CHU Paris IdF Ouest - Hôpital Raymond Poincaré
Unité : Consultation Maladies Neuro Musculaires

FRANCIA

ILE-DE-FRANCE
PARIS

European LeukoDataBase
CHU Paris - Hôpital Robert Debré
Centre de référence des leucodystrophies

FRANCIA

ILE-DE-FRANCE
PARIS

Financiado por un miembro del IRDiRCERN [EURO-NMD] - EURO-NMD Registry: Patient centered and interoperable registry hub for Rare Neuromuscular Diseases
Institut de Myologie - Hôpital Pitié-Salpêtrière
Unité clinique de pathologie neuromusculaire

ITALIA

VENETO
PADOVA

Financiado por un miembro del IRDiRCRegional registry for neuromuscular disorders
Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
Neuromuscular Laboratory

ITALIA

VENETO
PADOVA

Neuromuscular Tissue Bank (NMTB) (EuroBioBank partner)
Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
Neuromuscular Laboratory

PAISES BAJOS (LOS)

Gelderland
NIJMEGEN

Dutch Neuromuscular Database CRAMP: Computer Registry of All Myopathies and Polyneuropathies
Radboudumc - Radboud universitair medisch centrum
Afdeling Neurologie

PAISES BAJOS (LOS)

Limburg
MAASTRICHT

Biobank Intellectual Disability and Multiple Congenital Anomalies (DNA)
AZM - Academisch Ziekenhuis Maastricht
Afdeling Klinische Genetica

PAISES BAJOS (LOS)

Limburg
MAASTRICHT

Biobank Intellectual Disability and Multiple Congenital Anomalies (DNA)
AZM - Academisch Ziekenhuis Maastricht
Biobank Klinische Genetica Maastricht

PORTUGAL

SUL
LISBOA

Biobanco-IMM
Faculdade de Medicina da Universidade de Lisboa
Biobanco-IMM

REINO UNIDO (EL)

Cambridgeshire
CAMBRIDGE

UK10K RARE FIND - Familial Intellectual Disability variant database
Addenbrooke's Hospital
Familial Gastric Cancer - Addenbrookes

REINO UNIDO (EL)

Cambridgeshire
CAMBRIDGE

UK10K RARE FIND - Familial Intellectual Disability variant database
Wellcome Trust/MRC Building
Cambridge Institute for Medical Research

ALEMANIA

Baden-Württemberg
HEIDELBERG

iNTD (International Working Group on Neurotransmitter Related Disorders) Registry
Dietmar-Hopp-Stoffwechselzentrum
Klinik für Kinderheilkunde I - Stoffwechsellabor

ALEMANIA

Baden-Württemberg
HEIDELBERG

Financiado por un miembro del IRDiRCEIMD: European registry and network for intoxication type metabolic diseases
Zentrum für Kinder- und Jugendmedizin - Angelika-Lautenschläger-Klinik
Klinik für Kinderheilkunde I - Sektion für Neuropädiatrie und Stoffwechselmedizin

ALEMANIA

Baden-Württemberg
TÜBINGEN

Niemann-Pick Type C Disease Gene Variation Database
Institut für Medizinische Genetik und angewandte Genomik Tübingen
Institut für Medizinische Genetik und angewandte Genomik

ALEMANIA

Baden-Württemberg
TÜBINGEN

GeNeMove: CP2 Central DNA-Bank
Institut für Medizinische Genetik und angewandte Genomik Tübingen
Institut für Medizinische Genetik und angewandte Genomik

ALEMANIA

Baden-Württemberg
ULM

ALS registry swabia
Universitäts- und Rehabilitationskliniken Ulm (RKU)
Klinik für Neurologie

ALEMANIA

Bayern
MÜNCHEN

MD-NET: Muscle Tissue Culture Collection (MTCC) (EuroBioBank partner)
Friedrich-Baur-Institut
Friedrich-Baur-Institut an der Neurologischen Klinik und Poliklinik

ALEMANIA

Bayern
MÜNCHEN

Financiado por un miembro del IRDiRCTIRCON: NBIA (Neurodegeneration with Brain Iron Accumulation) patient registry
Friedrich-Baur-Institut
Friedrich-Baur-Institut an der Neurologischen Klinik und Poliklinik

ALEMANIA

Bayern
MÜNCHEN

Biobank for patient with NBIA - subproject of TIRCON
Institut für Humangenetik der TU München
Institut für Humangenetik

ALEMANIA

Bayern
MÜNCHEN

Neurobiobank Munique
Zentrum für Neuropathologie und Prionforschung (ZNP)
Zentrum für Neuropathologie und Prionforschung der LMU München

ALEMANIA

Bayern
WÜRZBURG

Brain-Net - brain tissue bank Würzburg (Amyotrophic lateral sclerosis)
Institut für Pathologie der Universität Würzburg
Institut für Pathologie

ALEMANIA

Hamburg
HAMBURG

NCL-Registry: International neuronal ceroid lipofuscinoses patient registry
UKE - Universitätsklinikum Hamburg-Eppendorf
Arbeitsgruppe Degenerative Gehirnkrankheiten

ALEMANIA

Hamburg
HAMBURG

Financiado por un miembro del IRDiRCMucopolysaccharidosis type 1 (MPS I) Registry - DE
UKE - Universitätsklinikum Hamburg-Eppendorf
Klinik und Poliklinik für Kinder- und Jugendmedizin

ALEMANIA

Hamburg
HAMBURG

Hunter Outcome Survey (HOS): patient registry - DE
UKE - Universitätsklinikum Hamburg-Eppendorf
Klinik und Poliklinik für Kinder- und Jugendmedizin

ALEMANIA

Hessen
MARBURG

GeNeMove: German database for wilson disease
Universitätsklinikum Gießen und Marburg GmbH, Standort Marburg
Klinik und Poliklinik für Neurologie

ALEMANIA

Nordrhein-Westfalen
AACHEN

Financiado por un miembro del IRDiRCEUROFA - EFACT: European Friedreich Ataxia Registry
Universitätsklinikum Aachen
Klinik für Neurologie

ALEMANIA

Nordrhein-Westfalen
AACHEN

EUROFA - EFACT: European Friedreich Ataxia Biobank
Universitätsklinikum Aachen
Klinik für Neurologie

ALEMANIA

Nordrhein-Westfalen
BONN

GEPARD: genebank of Parkinson's disease
Universitätsklinikum Bonn (AöR)
Klinik und Poliklinik für Neurologie

ALEMANIA

Nordrhein-Westfalen
ESSEN

ALS registry Nordrhein-Westfalen
Alfried Krupp Krankenhaus Rüttenscheid
Klinik für Neurologie

ALEMANIA

Nordrhein-Westfalen
MÜNSTER

ALEMANIA

Rheinland-Pfalz
LUDWIGSHAFEN

ALS registry Rheinland-Pfalz
Klinikum der Stadt Ludwigshafen gGmbH
Rheinland-Pfälzisches ALS-Register

ALEMANIA

Schleswig-Holstein
KIEL

Financiado por un miembro del IRDiRCCONNECT-GENERATE: National registry for autoimmune encephalitis
Universitätsklinikum Schleswig-Holstein - Campus Kiel
Klinik für Neurologie

AUSTRALIA

New South Wales
NORTH SYDNEY

Australian Motor Neurone Disease Registry (AMNDR)
Research Institute of Australia
Motor Neurone Disease

AUSTRALIA

Queensland
SOUTH BRISBANE

Global Angelman Syndrome Registry
Centre for Children's Health Research
Developmental Paediatrics Group, Mater Research

AUSTRIA

TIROL
INNSBRUCK

EMSA-SG: central patient registry of the European multiple system atrophy network
Medizinische Universität Innsbruck
Universitätsklinik für Neurologie

AUSTRIA

TIROL
INNSBRUCK

EMSA-SG: DNA bank of the European multiple system atrophy network
Medizinische Universität Innsbruck
Universitätsklinik für Neurologie

BELGICA

ANTWERPEN
ANTWERPEN

Inherited Peripheral Neuropathies Mutation Database - IPNMD
University of Antwerp - UA
Inherited Peripheral Neuropathies Mutation Database

BELGICA

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Belgian patient database for Wilson disease - contributes to the EuroWilson registry (terminated)
Cliniques universitaires Saint-Luc - UCLouvain
Service de gastro-entérologie et hépatologie pédiatrique

BELGICA

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

ENRAH: Belgian contribution to European registry for alternating hemiplegia in childhood [Terminated]
Secretariat Brussels, Postbus 10009
European Network for Research on Alternating Hemiplegia

BULGARIA

 South Central region
PLOVDIV

National registry of patients with Wilson disease - BG
BAPES - Bulgarian Association for Promotion of Education and Science
Information Centre for Rare Diseases and Orphan Drugs

BULGARIA

 South Central region
PLOVDIV

National registry of patients with mucopolysaccharidosis type II (MPS2) - BG
BAPES - Bulgarian Association for Promotion of Education and Science
Information Centre for Rare Diseases and Orphan Drugs

BULGARIA

 South-West region
SOFIA

National registry of patients with phenylketonuria - BG
University hospital of Obstetrics and Gynecology
Laboratory of molecular pathology - National Genetics Laboratory

DINAMARCA

Hovedstaden
COPENHAGEN

Nordic Database for Rare Diseases
Rigshospitalet
Department of Clinical Genetics and Paediatrics

DINAMARCA

Hovedstaden
HERLEV

Danish malignant hyperthermia registry - contributes to the European Malignant Hyperthermia Group (EMHG)
Herlev hospital - University of Copenhagen
Department of anaesthesiology - Danish Malignant Hyperthermia Centre - I 104 (LT)

DINAMARCA

Sjælland
COPENHAGEN

The PKU biobank as a national research source
Statens Serum Institut
Department of clinical biochemistry

ESPAÑA

Castilla - León
SALAMANCA

Banco Nacional de ADN: Colección de muestras de enfermedades raras
Centro de Investigación del Cáncer (USAL-CSIC)
Banco Nacional de ADN

ESTADOS UNIDOS

California
SAN FRANCISCO

Sjogren's International Collaborative Clinical Alliance registry
University of California
Department of Orofacial Sciences

ESTADOS UNIDOS

Massachusetts
CAMBRIDGE

HOS : Hunter Outcome Survey
Shire Human Genetics Therapies, Inc.

ESTADOS UNIDOS

Pennsylvania
EXTON

FARA: International Friedreich Ataxia Research Alliance registry
FARA - Friedreichs Ataxia Research Alliance

ESTADOS UNIDOS

Texas
DALLAS

Glucose transporter type 1 deficiency (G1D) Registry
Ut Southwestern Medical Center
Department of Neurology and Neurotherapeutics

FRANCIA

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

DNA and cells bank for alternating hemiplegia of childhood
Institution: Information not provided - FR

FRANCIA

AUVERGNE-RHONE-ALPES
BRON

EDMUS - NOMADMUS: French cohort of Devic's neuromyelitis optica and related neurological disorders
CHU de Lyon HCL - GH Est
Centre de Ressources Biologiques - NeuroBioTec

FRANCIA

AUVERGNE-RHONE-ALPES
BRON

EDMUS: European Database for Multiple Sclerosis and other related diseases
CHU de Lyon HCL - GH Est
Service de Neurologie A - EDMUS Coordinating Center

FRANCIA

ILE-DE-FRANCE
LE KREMLIN-BICÊTRE

Financiado por un miembro del IRDiRCRaDiCo-IDMet: National and European cohort on Imprinting Disorders and their metabolic consequences
Hôpital Bicêtre, GHU APHP. Université Paris Saclay
Service d'Endocrinologie et Diabète de l'Enfant

FRANCIA

ILE-DE-FRANCE
PARIS

EU-CHS: European central hypoventilation syndrome registry
CHU Paris - Hôpital Robert Debré
Equipe "Physiopathologie et neuroprotection des atteintes du cerveau en développement"

FRANCIA

ILE-DE-FRANCE
PARIS

French central hypoventilation syndrome registry - will contribute to the European CHS registry
CHU Paris - Hôpital Robert Debré
Equipe "Physiopathologie et neuroprotection des atteintes du cerveau en développement"

FRANCIA

ILE-DE-FRANCE
PARIS

Financiado por un miembro del IRDiRCRaDiCo-IDMet: National and European cohort on Imprinting Disorders and their metabolic consequences
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
Service Explorations fonctionnelles Endocriniennes

FRANCIA

ILE-DE-FRANCE
PARIS

French Cohorts in Sneddon syndrome and suspected Sneddon syndrome livedo
Groupe hospitalier AP-HP.6 - Hôpital Tenon
Service de dermatologie, médecine vasculaire et allergologie

FRANCIA

ILE-DE-FRANCE
PARIS

UMD ATP7B (ATPase, Cu++ transporting, beta polypeptide) mutations database
Hôpital Necker-Enfants Malades
Biochimie Métabolomique et Protéomique

FRANCIA

ILE-DE-FRANCE
PARIS

Motor Function Measure database (Neuromuscular Diseases)
Institut de Myologie - Hôpital Pitié-Salpêtrière
Unité clinique de pathologie neuromusculaire

FRANCIA

NOUVELLE AQUITAINE
LIMOGES

French Register of Amyotrophic Lateral Sclerosis
Faculté de médecine de Limoges
NeuroEpidémiologie Tropicale

FRANCIA

OCCITANIE
MONTPELLIER

French registry of rare hypersomnias
CHU de Montpellier - Hôpital Gui de Chauliac
Unité des Troubles du sommeil et de l'éveil

GRECIA

ATTIKI
ATHENS

PATIENT REGISTRY AND DNA BIOBANK ON NEUROGENETIC DISORDERS
University of Athens - Medical school
Neurogenetics Unit

HUNGRIA

Dél-Dunántúl
PECS

Friedreich ataxia biobank
Clinical Center - University of Pécs
Department of Medical Genetics

IRLANDA

County Dublin
DUBLIN

Hunter Outcome Survey (HOS): patient registry
Children's Health Ireland @ Temple Street
National Centre for Inherited Metabolic Disorders

IRLANDA

County Dublin
DUBLIN

Financiado por un miembro del IRDiRCIrish Registry for homocystinurias and methylation defects - contributes to E-HOD
Children's Health Ireland @ Temple Street
National Centre for Inherited Metabolic Disorders

IRLANDA

County Dublin
DUBLIN

Irish registry of amyotrophic lateral sclerosis and motor neurone disease - contributes to Euro-MOTOR
Trinity College Dublin
Department of Neurology - Trinity Biomedical Sciences Institute

ITALIA

CAMPANIA
NAPOLI

Bank for the Diagnosis and Research on neuromuscular Disorders (NHMGB) (EuroBioBank partner)
AOU Università degli Studi della Campania "Luigi Vanvitelli" - Centro storico
Servizio di Cardiomiologia e Genetica Medica

ITALIA

LIGURIA
GENOVA

Galliera Genetic Bank
Ospedali Galliera
Dipartimento di Scienze genetiche, Perinatali e Ginecologiche

ITALIA

LOMBARDIA
BERGAMO

Angelman Syndrome Italian Registry (RISA)
ASST Papa Giovanni XXIII
Fondazione per la Ricerca dell'Ospedale di Bergamo

ITALIA

LOMBARDIA
BOSISIO PARINI

ITALIA

LOMBARDIA
BOSISIO PARINI

IBAHC: Italian registry for alternating hemiplegia of childhood
IRCCS "E. Medea"
Laboratorio di Biologia Molecolare

ITALIA

LOMBARDIA
MILANO

Human DNA bank of patients affected by Parkinson disease and parkinsonisms
ASST Nord Milano
Parkinson Institute-Centro parkinson

ITALIA

LOMBARDIA
MILANO

GLUT1 deficiency syndrome registry
Associazione Italiana GLUT1

ITALIA

LOMBARDIA
MILANO

DNA cell lines and nerve muscle cardiac tissues bank (EuroBioBank partner)
Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico
U.O. Malattie Neuromuscolari

ITALIA

LOMBARDIA
MILANO

Movement Disorders Biobank (EuroBioBank partner)
Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
U.O. di Neurogenetica Molecolare

ITALIA

LOMBARDIA
SAN DONATO MILANESE

Italian registry of muscular channelopathy
IRCCS Policlinico San Donato
U.O. di Neurologia - Centro per lo Studio delle Malattie Neuromuscolari

ITALIA

PIEMONTE
TORINO

ITALIA

PUGLIA
SAN GIOVANNI ROTONDO

Genetic Biobank from patients with Williams-Beuren syndrome and other genomic disorders
IRCCS Ospedale Casa Sollievo della Sofferenza -Poliamb. Giovanni Paolo II
U.O.C. Genetica Medica

ITALIA

SICILIA
CATANIA

EUROWILSON: Registry and network to improve the management of Wilson Disease
Presidio Ospedaliero Garibaldi-Nesima
Servizio di Genetica Medica - Centro di Riferimento per la Prevenzione, la Diagnosi e la Cura delle Malattie Genetiche Rare

ITALIA

TOSCANA
PISA

Italian Registry of Kernicterus and hyperbilirubinemia
Fondazione "Gabriele Monasterio" - Consiglio Nazionale delle Ricerche CNR
Fondazione Toscana Gabriele Monasterio

NORUEGA

Nord-Norge
TROMSØ

HUE-MAN patient registry on alpha mannosidosis
UNN - Universitetssykehuset Nord-Norge
Department of medical genetics

NORUEGA

Nord-Norge
TROMSØ

HUE-MAN mutation registry on alpha mannosidosis
UNN - Universitetssykehuset Nord-Norge
Department of medical genetics

NORUEGA

Nord-Norge
TROMSØ

HUE-MAN biobank on alpha mannosidosis
UNN - Universitetssykehuset Nord-Norge
Department of medical genetics

PAISES BAJOS (LOS)

Gelderland
NIJMEGEN

Financiado por un miembro del IRDiRCERN [eUROGEN] - ERN eUROGEN Registry for rare urogenital diseases
Radboudumc - Radboud universitair medisch centrum
Afdeling Kinderurologie

PAISES BAJOS (LOS)

Gelderland
NIJMEGEN

Financiado por un miembro del IRDiRCERN [eUROGEN] - ERN eUROGEN Registry for rare urogenital diseases
Radboudumc - Radboud universitair medisch centrum
Afdeling Health Evidence

PAISES BAJOS (LOS)

Limburg
MAASTRICHT

Biobank Myotonic Dystrophy type 1 (DNA, serum, fibroblasts and pericytes)
AZM - Academisch Ziekenhuis Maastricht
Afdeling Neurologie

PAISES BAJOS (LOS)

Limburg
MAASTRICHT

Biobank Myotonic Dystrophy type 1 (DNA, serum, fibroblasts and pericytes)
AZM - Academisch Ziekenhuis Maastricht
Biobank Klinische Genetica Maastricht

PAISES BAJOS (LOS)

Noord-Holland
AMSTERDAM

Dutch patient registry for Niemann-Pick Disease Type C
Amsterdam UMC, locatie AMC
Afdeling Erfelijke Stofwisselingsziekten

PAISES BAJOS (LOS)

Noord-Holland
AMSTERDAM

The ALD Connect Patient Portal
Amsterdam UMC, locatie AMC
Laboratorium Genetische Metabole Ziekten

PAISES BAJOS (LOS)

Noord-Holland
AMSTERDAM

PAISES BAJOS (LOS)

Noord-Holland
AMSTERDAM

PAISES BAJOS (LOS)

Noord-Holland
NAARDEN

The international Mps I registry
Genzyme Europe B.V.

PAISES BAJOS (LOS)

Noord-Holland
NAARDEN

PAISES BAJOS (LOS)

Utrecht
UTRECHT

ALS database
UMC Utrecht - Universitair Medisch Centrum Utrecht
Afdeling Neurologie

PAISES BAJOS (LOS)

Zuid-Holland
LEIDEN

Leiden Narcolepsy Biobank (DNA, serum, CSF and peripheral blood cells)
LUMC - Leids Universitair Medisch Centrum
Afdeling Neurologie

PAISES BAJOS (LOS)

Zuid-Holland
LEIDEN

LUMC Biobank Hemiplegic Migraine (DNA/plasma/serum/cell lines/CSF)
LUMC - Leids Universitair Medisch Centrum
Afdeling Neurologie

PAISES BAJOS (LOS)

Zuid-Holland
ROTTERDAM

ENCORE Biobank for Neurodevelopmental Disorders (blood/saliva/skin biopsies)
Erasmus MC - Erasmus Medisch Centrum
Afdeling Neurowetenschappen

PAISES BAJOS (LOS)

Zuid-Holland
ROTTERDAM

POLONIA

Warszawa
WARSAW

Polish Registry of Patients with Neuromuscular Diseases contributes to the TREAT-NMD network
Warszawski Uniwersytet Medyczny - Medical University of Warsaw
Klinika Neurologii - Department of Neurology

PORTUGAL

NORTE
PORTO

MitoBreak: The mitochondrial DNA breakpoints database.
CIIMAR - Interdisciplinary Centre of Marine and Environmental Research

REINO UNIDO (EL)

Cambridgeshire
CAMBRIDGE

European Prader-Willi syndrome database
Developmental Psychiatry - University of Cambridge
Learning Disabilities Research Group

REINO UNIDO (EL)

Greater London
LONDON

BPOLD: British Paediatric Orphan Lung Disease Registry
GOSH NHS Foundatin Trust
Respiratory Medicine Group

REINO UNIDO (EL)

Greater London
LONDON

Batten Disease Neuronal Ceroid Lipofuscinosis (NCL) Patient Registry
UCL University College London
MRC Laboratory for Molecular Cell Biology

REINO UNIDO (EL)

Greater Manchester
MANCHESTER

Registry for Patients with Niemann-Pick Type C Disease
St Mary's Hospital
Manchester Cente for Genomic Medicine

REINO UNIDO (EL)

Lothian
EDINBURGH

BPOLD: British Paediatric Orphan Lung Disease Registry
Royal Hospital for Sick Children
Department of Respiratory, Sleep & General Medicine

REINO UNIDO (EL)

South Yorkshire
SHEFFIELD

EURO WILSON: Creating a European Clinical Database and designing randomised controlled clinical trials for Wilson disease - UK
The Sheffield Children's Hospital
Sheffield Children's Hospital (Division of Child Health)

REINO UNIDO (EL)

Staffordshire
STOKE ON TRENT

UK Registry for Central Hypoventilation Syndrome (CHS)
University Hospital of North Staffordshire - Cheethams Children's Centre
UK Central Hypoventilation Syndrome Registry

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE UPON TYNE

UK Myotonic dystrophy type I patient registry (part of the TREAT-NMD network)
Newcastle upon Tyne Hospitals NHS Trust
John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE-UPON-TYNE

United Kingdom Primary Sjogren's Syndrome Registry
Faculty of Medical Sciences Newcastle University
Musculoskeletal Research Group Institute of Cellular Medicine

REINO UNIDO (EL)

West Midlands
BIRMINGHAM

Financiado por un miembro del IRDiRCEIMD: European registry and network for intoxication type metabolic diseases
Birmingham Children's Hospital NHS Foundation Trust
Department of Clinical Inherited Metabolic Disorders

REINO UNIDO (EL)

West Midlands
BIRMINGHAM

Financiado por un miembro del IRDiRCInternational Niemann-Pick Disease Registry
Queen Elizabeth Hospital
Inherited Metabolic Disorders

REPUBLICA CHECA (LA)

South Moravia
BRNO

Autoimmune neuromuscular disease
Masaryk University
Department of Neurology

SUECIA

Region Skåne
LUND

LYSTbase: Mutation registry for Chediak-Higashi syndrome (previously known as CHS1base)
Lund University
Department of Experimental Medical Science

SUIZA

Suisse Alémanique
BASEL

SACHER: Swiss Adult Congenital HEart disease Registry
Universitätsspital Basel
Cardiology Department

ALEMANIA

Baden-Württemberg
TÜBINGEN

Financiado por un miembro del IRDiRCMEFOPA: registry for patients with rare Mendelian forms of Parkinson's Disease -terminated-
Hertie-Institut für klinische Hirnforschung (HIH)
Abteilung Neurologie mit Schwerpunkt neurodegenerative Erkrankungen

ALEMANIA

Baden-Württemberg
TÜBINGEN

MEFOPA-biobank for patients with rare Mendelian forms of Parkinson's Disease
Hertie-Institut für klinische Hirnforschung (HIH)
Abteilung Neurologie mit Schwerpunkt neurodegenerative Erkrankungen

ALEMANIA

Baden-Württemberg
TÜBINGEN

EUROSCA-R: European patient registry on spinocerebellar ataxias
Institut für Medizinische Genetik und angewandte Genomik Tübingen
Institut für Medizinische Genetik und angewandte Genomik

ALEMANIA

Baden-Württemberg
TÜBINGEN

EUROSCA-R: European biobank on spinocerebellar ataxias
Institut für Medizinische Genetik und angewandte Genomik Tübingen
Institut für Medizinische Genetik und angewandte Genomik

ALEMANIA

Baden-Württemberg
ULM

Enroll-HD Registry
Universitäts- und Rehabilitationskliniken Ulm (RKU)
Zentrale Koordination des Europäischen HD Netzwerks

ALEMANIA

Baden-Württemberg
ULM

Enroll-HD Biobank
Universitäts- und Rehabilitationskliniken Ulm (RKU)
Zentrale Koordination des Europäischen HD Netzwerks

ALEMANIA

Bayern
MÜNCHEN

Financiado por un miembro del IRDiRCGerman CMT-patient registry germany - part of the TREAT-NMD network
Friedrich-Baur-Institut
TREAT-NMD-Patientenregister

ALEMANIA

Bayern
MÜNCHEN

EHDN: neuroacanthocytosis patient registry
LMU Klinikum der Universität München - Campus Großhadern
Arbeitsgruppe Kognitive Neurologie - Neurologische Klinik und Poliklinik

ALEMANIA

Hamburg
HAMBURG

Registry for Patients with WT1 Mutation Associated Diseases
UKE - Universitätsklinikum Hamburg-Eppendorf
Klinik und Poliklinik für Kinder- und Jugendmedizin

ALEMANIA

Niedersachsen
GÖTTINGEN

German TSE research platform: establishment of a national CJD sample bank
Universitätsmedizin Göttingen
Prionforschungsgruppe

ALEMANIA

Nordrhein-Westfalen
AACHEN

Financiado por un miembro del IRDiRCCMT- Net: National biobank
Universitätsklinikum Aachen
Institut für Neuropathologie

ALEMANIA

Nordrhein-Westfalen
BONN

EUROSCA-R: European patient registry on spinocerebellar ataxias
Universitätsklinikum Bonn (AöR)
Klinik und Poliklinik für Neurologie

ALEMANIA

Nordrhein-Westfalen
BONN

EUROSCA-R: European biobank on spinocerebellar ataxias
Universitätsklinikum Bonn (AöR)
Klinik und Poliklinik für Neurologie

ALEMANIA

Nordrhein-Westfalen
BONN

European registry of sporadic degenerative ataxia with adult onset
Universitätsklinikum Bonn (AöR)
Klinik und Poliklinik für Neurologie

ALEMANIA

Nordrhein-Westfalen
DÜSSELDORF

Neuromyelitis optica patient registry
Universitätsklinikum Düsseldorf
Neuromyelitis optica Studiengruppe (NEMOS)

ALEMANIA

Rheinland-Pfalz
MAINZ

Mainz registry of congenital anomalies - contributes to the EUROCAT network
Universitätsmedizin Mainz
Geburtenregister Mainzer Modell

ALEMANIA

Sachsen-Anhalt
MAGDEBURG

Centre Saxony-Anhalt registry of congenital anomalies - contributes to the EUROCAT network
Universitätsklinikum Magdeburg A.ö.R
MONZ - Fehlbildungsmonitoring Sachsen-Anhalt

ALEMANIA

Schleswig-Holstein
LÜBECK

Financiado por un miembro del IRDiRCDYSTRACT: German Dystonia Registry
Universität Lübeck
Institut für Neurogenetik

AUSTRALIA

New South Wales
WESTMEAD

RettBASE: RettSyndrome.org variation database
University of Sydney
Children's Hospital - Paediatrics and Child Health

AUSTRALIA

Victoria
MEKBOURNE

Myeloma and Related Diseases Registry (MRDR)
Monash University
Department of Epidemiology & Preventive Medicine

AUSTRIA

OBERÖSTERREICH
LINZ

Non-Interventional, web-based Registry for Histiocytic Disorders
Ordensklinikum Linz GmbH Elisabethinen
Interne 1 - Hämatologie mit Stammzelltransplantation, Hämostaseologie und medizinische Onkologie

AUSTRIA

STEIERMARK
GRAZ

Styrian registry of congenital anomalies - contributes to the EUROCAT network
Medizinische Universität Graz
Forschungsverein zur Registrierung steirischer Geburtsfehlbildungen

BELGICA

ANTWERPEN
ANTWERPEN

Antwerpen registry of congenital anomalies - contributes to the EUROCAT network
Provinciaal Instituut voor Hygiëne (PIH)- Antwerpen
EUROCAT Belgium_Antwerpen

BELGICA

HAINAUT
GOSSELIES

Hainaut and Namur registry of congenital anomalies - contributes to the EUROCAT network
Institut de Pathologie et de Génétique
Département de Génétique Clinique - Institut de Pathologie et de Génétique (IPG)

BELGICA

OOST-VLAANDEREN
GENT

I-DSD: International Disorders of Sex Development registry - Flanders contribution (Ghent university hospital)
Ghent University Hospital - UZ Gent
Het Centrum voor geslachtsontwikkeling [DSD team] - UZ Gent

CANADA

Colombie-Britannique
VANCOUVER

Glomerulonephritis Registry
Centre for Health Evaluation and Outcome Sciences (CHEOS)
Department of Nephrology

DINAMARCA

Syddanmark
ODENSE

Funen county registry of congenital anomalies - contributes to the EUROCAT network
University of Southern Denmark
Epidemiology department

ESPAÑA

Asturias
OVIEDO

Registro MEN: Registro de Neoplasias Endocrinas Múltiples, Feocromocitomas y Paragangliomas
Hospital Universitario Central de Asturias
Servicio de Endocrinología y Nutrición

ESPAÑA

Cataluña
BELLATERRA

Biobanco de reparación del DNA
Universitat Autònoma de Barcelona
Grupo de inestabilidad genómica y reparación del DNA

ESPAÑA

Comunidad Valenciana
VALENCIA

Financiado por un miembro del IRDiRCTREAT-CMT: Base de datos de mutaciones CMT en la población española
Centro de Investigación Príncipe Felipe (CIPF)
Unidad de Genética y Genómica de Enfermedades Neuromusculares y Neurodegenerativas

ESPAÑA

Madrid
MADRID

Financiado por un miembro del IRDiRCRegistro Nacional de Encefalopatías Espongiformes Transmisibles Humanas
Centro Nacional de Epidemiología (CNE)
Area de Epidemiología Aplicada

ESPAÑA

País Vasco
VITORIA-GASTEIZ

ESTADOS UNIDOS

Georgia
ATLANTA

CMDIR: congenital muscular dystrophy international registry
Emory University
Woodruff Health Sciences Center

ESTADOS UNIDOS

Virginia
CHARLOTTESVILLE

GNAO1 International Patient Registry
University of Virginia Health System
Department of Neurology

FINLANDIA

Finland
HELSINKI

Register of Congenital Malformations
Terveyden ja hyvinvoinnin laitos (THL)
Finnish Institute for Health and Welfare (THL)

FRANCIA

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

French registry of Kabuki syndrome
Institution: Information not provided - FR

FRANCIA

AUVERGNE-RHONE-ALPES
BRON

EDMUS - NOMADMUS: French biobank of Devic's neuromyelitis optica and related neurological disorders
CHU de Lyon HCL - GH Est
Centre de Ressources Biologiques - NeuroBioTec

FRANCIA

AUVERGNE-RHONE-ALPES
CLERMONT-FERRAND

Auvergne registry of congenital anomalies - contributes to the EUROCAT network
CHU de Clermont-Ferrand - Hôpital d'Estaing
Service de génétique médicale

FRANCIA

AUVERGNE-RHONE-ALPES
LYON

Rhône-Alpes registry of congenital anomalies - contributes to the EUROCAT network
Registre des Malformations en Rhône Alpes
Registre des Malformations en Rhône Alpes REMERA

FRANCIA

BRETAGNE
RENNES

FRANCIA

BRETAGNE
RENNES

French registry of Iron overload genetic rare diseases, non-related to the HFE gene
CHU de Rennes - Hôpital Pontchaillou
Service des maladies du foie

FRANCIA

CENTRE-VAL DE LOIRE
TOURS

NF-France: genotype/phenotype database on neurofibromatosis 1
CHRU de Tours - Hôpital Clocheville
Pôle Enfants - Neuropédiatrie et handicaps

FRANCIA

GRAND-EST
REIMS

CRB TOXOPLASMA: biological resources centre - Toxoplasma
UFR de Médecine de Reims IFR 53
Protozooses transmises par l'alimentation (Cryptosporidiose, Giardiose et Toxoplasmose)

FRANCIA

GRAND-EST
STRASBOURG

UMD CSA (ERCC8) mutations database
CHU de Strasbourg - Hôpital de Hautepierre
Service de Neuropédiatrie

FRANCIA

GRAND-EST
STRASBOURG

UMD CSB (ERCC6) mutations database
CHU de Strasbourg - Hôpital de Hautepierre
Service de Neuropédiatrie

FRANCIA

HAUTS-DE-FRANCE
LOMME

French registry of tetrahydrobiopterin deficiencies
Hôpital Saint-Philibert
Laboratoire de biochimie

FRANCIA

ILE-DE-FRANCE
CRÉTEIL

NF-France: genotype/phenotype database on neurofibromatosis 1
Hôpitaux Universitaires Henri Mondor
Service de dermatologie

FRANCIA

ILE-DE-FRANCE
PARIS

FRANCIA

ILE-DE-FRANCE
PARIS

SYRENE: Rett syndrome network - French database of clinical and genetic aspects of Rett syndrome
Hôpital Necker-Enfants Malades
Service de Neurologie pédiatrique

FRANCIA

OUTRE-MER
FORT DE FRANCE

French West Indies registry of congenital anomalies - contributes to the EUROCAT network
CHU de Martinique - Maison de la Femme, de la Mère et de l'Enfant
Centre Pluridisciplinaire de Diagnostic Prénatal (CPDP)

FRANCIA

OUTRE-MER
SAINT-PIERRE

La Réunion Fench Island registry of congenital anomalies - contributes to the EUROCAT network
CHU de la Réunion - GH Sud Réunion - Saint-Pierre
Service de Génétique Médicale

HUNGRIA

Dél-Dunántúl
PECS

Huntington disease biobank
Clinical Center - University of Pécs
Department of Medical Genetics

HUNGRIA

Dél-Dunántúl
PECS

Neurofibromatosis type 1 biobank
Clinical Center - University of Pécs
Department of Medical Genetics

HUNGRIA

Dél-Dunántúl
PECS

Rett syndrome biobank
Clinical Center - University of Pécs
Department of Medical Genetics

HUNGRIA

Dél-Dunántúl
PECS

Spinocerebellar ataxia biobank
Clinical Center - University of Pécs
Department of Medical Genetics

HUNGRIA

Dél-Dunántúl
PECS

Tuberous sclerosis biobank
Clinical Center - University of Pécs
Department of Medical Genetics

HUNGRIA

Közép-Magyarország
BUDAPEST

National NF Register
Nemzeti NF Regiszter
NF Magyarorszag

IRLANDA

County Cork
CORK

IRLANDA

County Dublin
DUBLIN

Dublin registry of congenital anomalies - contributes to the EUROCAT network
Dr. Steeven's Hospital
HSE Registry of Congenital Anomalies (East)

IRLANDA

County Kilkenny
KILKENNY

South East of Ireland registry of congenital anomalies - part of BINOCAR and EUROCAT network
Health Service Executive South SE
South East of Ireland registry of congenital anomalies

ITALIA

CAMPANIA
BENEVENTO

Campania registry of congenital anomalies - contributes to the EUROCAT network
A.O.R.N. "Gaetano Rummo"
U.O.C. di Genetica Medica

ITALIA

EMILIA ROMAGNA
REGGIO EMILIA

Ring14 Clinical database
Associazione Internazionale Ring 14 ONLUS

ITALIA

LAZIO
ROMA

Italian registry of Creutzfeldt-Jakob disease and correlated syndromes
ISS - Istituto Superiore di Sanità
Dipartimento di Biologia Cellulare e Neuroscienze

ITALIA

SICILIA
CATANIA

ISMAC: Sicilian registry of congenital anomalies - contributes to the EUROCAT network
ASMAC
Associazione per la Prevenzione Sociale e per il Trattamento delle Malformazioni Congenite

ITALIA

TOSCANA
PISA

Tuscan Registry of Congenital Anomalies
Fondazione "Gabriele Monasterio" - Consiglio Nazionale delle Ricerche CNR
Unità di Ricerca Epidemiologia Ambientale e Registri di Patologia

ITALIA

TOSCANA
SIENA

Cells lines and DNA bank of Rett syndrome and other X-linked mental retardation
Azienda Ospedaliera Universitaria Senese - Policlinico Santa Maria alle Scotte
U.O.C. di Genetica Medica

ITALIA

TOSCANA
SIENA

Rett Syndrome Database
Azienda Ospedaliera Universitaria Senese - Policlinico Santa Maria alle Scotte
U.O.C. di Genetica Medica

ITALIA

VENETO
PADOVA

North-east Italy registry of neurofibromatosis
Azienda Ospedaliera di Padova
U.O.C. Genetica Clinica ed Epidemiologica

ITALIA

VENETO
PADOVA

North-East of Italy registry of congenital anomalies - contributes to the EUROCAT network
Azienda Ospedaliera di Padova
U.O.C. Genetica Clinica ed Epidemiologica

MALTA

MALTA
G'MANGIA

MALTA CONGENITAL ANOMALIES REGISTRY (MCAR) - it contributes to EUROCAT
Ministry for Health
Directorate of Health Information and Research

PAISES BAJOS (LOS)

Gelderland
NIJMEGEN

AGORA: biobank (DNA) for congenital anomalies and childhood cancer
Radboudumc - Radboud universitair medisch centrum
Afdeling Kinderurologie

PAISES BAJOS (LOS)

Gelderland
NIJMEGEN

AGORA: biobank (DNA) for congenital anomalies and childhood cancer
Radboudumc - Radboud universitair medisch centrum
Afdeling Health Evidence

PAISES BAJOS (LOS)

Groningen
GRONINGEN

EUROCAT Northern Netherlands - contributes to the international EUROCAT network
UMCG - Universitair Medisch Centrum Groningen
Afdeling Genetica

PAISES BAJOS (LOS)

Noord-Holland
AMSTERDAM

Biobank CEEx study (fibroblasts)
Amsterdam UMC, locatie AMC
Kinderpolikliniek Klinische Genetica

PAISES BAJOS (LOS)

Noord-Holland
AMSTERDAM

Biobank CEEx study (fibroblasts)
Amsterdam UMC, locatie AMC
Polikliniek Algemene Kindergeneeskunde

PAISES BAJOS (LOS)

Zuid-Holland
LEIDEN

LUMC Biobank RVCL-S (DNA/peripheral blood cells/plasma/serum/tissue/CSF)
LUMC - Leids Universitair Medisch Centrum
Afdeling Neurologie

POLONIA

Poznan
POZNAN

PRCM: Polish registry of congenital malformations - contributes to the EUROCAT network
Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu
Zaklad Genetyki Medycznej

PORTUGAL

NORTE
PORTO

Portuguese Rett syndrome registry
Hospital de Santo António - Centro Hospitalar do Porto
Serviço de Pediatria Médica

PORTUGAL

SUL
LISBOA

RENAC - Portuguese registry of congenital anomalies (contributes to the EUROCAT network)
Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
Departamento de Epidemiologia

REINO UNIDO (EL)

East Sussex
BRIGHTON

TuberOus SClerosis registry to increase disease Awareness (TOSCA)
Royal Sussex County Hospital
Sussex Kidney Unit

REINO UNIDO (EL)

Hampshire
SOUTHAMPTON

WANDA - Wessex registry of antenatally detected anomalies - part of BINOCAR and EUROCAT network
Princess Anne Hospital
Paediatric Endocrinology and the Wessex Clinical Genetics Service

REINO UNIDO (EL)

Merseyside
LIVERPOOL

United Kingdom neuromyelitis optica registry
The Walton Centre NHS Foundation Trust
The Walton Centre for Neurology and Neurosurgery

REINO UNIDO (EL)

Nottinghamshire
NOTTINGHAM

Ataxia-Telangiectasia International Registry (A-T Society)
William Whitehouse
Pediatric Neurology Department

REINO UNIDO (EL)

Oxfordshire
OXFORD

UK10K RARE CHD - Congenital heart disease variant database
The Wellcome Trust Centre for Human Genetics
Division of Cardiovascular Medicine

REINO UNIDO (EL)

South Yorkshire
SHEFFIELD

EHDN: registry of juvenile Huntington's disease
The Sheffield Children's Hospital
Sheffield Clinical Genetics Department (part of the Sheffield Clinical Genetics Service)

REINO UNIDO (EL)

Tayside
EDINBURGH

Rett Syndrome Mutation Database: MeCP2 gene
MRC Centre for Regenerative Medicine
Institute for Stem Cell Research

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE UPON TYNE

Global FKRP registry (Global Fukutin-Related Protein defects registry) - Part of TREAT-NMD Alliance
Institute of Genetic Medicine - International Centre for Life
Global FKRP Registry

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE UPON TYNE

Global FKRP registry (Global Fukutin-Related Protein defects registry) - Part of TREAT-NMD Alliance
Newcastle upon Tyne Hospitals NHS Trust
John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE UPON TYNE

International A-T Registry
Newcastle upon Tyne Hospitals NHS Trust
John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine

SUECIA

Region Skåne
LUND

MYO5Abase: Mutation registry for Griscelli syndrome, type 1 (GS1)
Lund University
Department of Experimental Medical Science

SUECIA

Region Skåne
LUND

SUECIA

Region Skåne
LUND

STX11base: Mutation registry for Familial haemophagocytic lymphohistiocytosis 4 (FHL4)
Lund University
Department of Experimental Medical Science

SUECIA

Region Skåne
LUND

UNC13Dbase: Mutation registry for Familial hemophagocytic lymphohistiocytosis 3
Lund University
Department of Experimental Medical Science

SUECIA

Region Skåne
LUND

CD59base: Mutation registry for CD59 deficiency
Lund University
Department of Experimental Medical Science

SUECIA

Region Skåne
LUND

TLR3base: Mutation registry for Influenza-associated encephalopathy
Lund University
Department of Experimental Medical Science

SUECIA

Region Skåne
LUND

UNC93B1base: Mutation registry for UNC93B deficiency (Herpes simplex encephalitis)
Lund University
Department of Experimental Medical Science

SUECIA

Region Stockholm
HUDDINGE

Swedish and Finnish registry of CADASIL patients
Karolinska Institutet - Huddinge
Department of Neurobiology, Care Sciences and Society

SUIZA

Suisse Alémanique
BERN

Swiss Paediatric Renal Registry
Institute of Social and Preventive Medicine (ISPM)

SUIZA

Suisse Alémanique
ZÜRICH

BH4: international mutation registry of tetrahydrobiopterin deficiency
Universitäts - Kinderspital Zürich - Eleonorenstiftung
Abteilung für Stoffwechselkrankheiten

SUIZA

Suisse Romande
LAUSANNE

Swiss registries for Interstitial and Orphan Lung Diseases (SIOLD Registries)
Centre Hospitalier Universitaire Vaudois CHUV
Swiss registries for Interstitial and Orphan Lung Diseases

SUIZA

Suisse Romande
LAUSANNE

EUROCAT VAUD Switzerland - Registry of congenital malformations of canton Vaud
Centre Hospitalier Universitaire Vaudois CHUV
Département Femme-Mère-Enfant - Maternité

CANADA

Ontario
BRAMPTON

Fragile X Patient Registry
FXRFC
Fragile X Research Foundation of Canada

CANADA

Québec
MONTRÉAL

Canadian Inflammatory Myopathy Study (CIMS)
Hôpital général juif - Jewish General Hospital
Rheumatology Department, Suite A 725

CANADA

Québec
MONTRÉAL

Canadian Inflammatory Myopathy Study (CIMS)
Montreal Neurological Institute and Hospital
Clinical Research Unit (CRU)

CROACIA

CROATIA
ZAGREB

Registry for neuromuscular disease
University Hospital Centre Zagreb
Department of Child Neurology

ESPAÑA

Cataluña
BARCELONA

Registro de pacientes Atrofia Muscular Espinal España - parte de la red TREAT-NMD
Hospital Universitari Vall d'Hebron
Laboratorio de Genética

FINLANDIA

Finland
TURKU

FRANCIA

GRAND-EST
STRASBOURG

Mutation registry of the Coffin-Lowry syndrome
CHU de Strasbourg - Hôpital Civil
Laboratoire de diagnostic génétique

FRANCIA

ILE-DE-FRANCE
PARIS

Financiado por un miembro del IRDiRCRaDiCo-PP: National cohort on periodic paralysis : clinical, genetic and medico-economic studies involving m-health monitoring tools
APHP.Sorbonne Université, Hôpital de la Pitié-Salpêtrière
Unité Neurogénétique et métabolisme

FRANCIA

ILE-DE-FRANCE
PARIS

French registry for macrophagic myofasciitis
APHP.Sorbonne Université, Hôpital de la Pitié-Salpêtrière
Département de Médecine Interne et Immunologie Clinique (DMIIC)

FRANCIA

ILE-DE-FRANCE
PARIS

French auto-immunity and Rituximab (AIR) registry: prospective study of patients treated with Rituximab
CHU Paris Centre - Hôpital Cochin, Site Cochin
Unité fonctionnelle de Médecine interne et centre de référence maladies rares

FRANCIA

NORMANDIE
ROUEN

UMD-SMN1 France
CHU de Rouen
Laboratoire de génétique moléculaire

HUNGRIA

Dél-Dunántúl
PECS

Epilepsy biobank
Clinical Center - University of Pécs
Department of Medical Genetics

HUNGRIA

Közép-Magyarország
BUDAPEST

SMA registry Hungary - contributes to the TREAT-NMD network
National Institute of Environmental Health
Department of Molecular Genetics and Diagnostics

IRLANDA

County Dublin
DUBLIN

Irish Dystonia DNA Biobank
St. Vincent's University Hospital
Department of Neurology

ITALIA

CAMPANIA
NAPOLI

Naples Human Mutation Gene Biobank
AOU Università degli Studi della Campania "Luigi Vanvitelli" - Centro storico
Servizio di Cardiomiologia e Genetica Medica

ITALIA

LOMBARDIA
MILANO

RAM-NET: Italian registry of patients with neuromuscular diseases - contributes to Treat-NMD european network
Fondazione IRCCS Istituto Neurologico "Carlo Besta"
Clinica Neuropatie Degenerative Centrali e Periferiche

ITALIA

PIEMONTE
NOVARA

BIODEF-International Database of tetrahydrobiopterin Deficiencies
Università degli Studi del Piemonte Orientale
Laboratorio di Patologia Genetica

ITALIA

SICILIA
MESSINA

Financiado por un miembro del IRDiRCTransthyretin amyloid neuropathy (TTR-FAP) italian registry
A.O.U. Policlinico "G. Martino"
Centro Clinico Nemo Sud - Centro ad alta specializzazione per le malattie neuromuscolari

ITALIA

TOSCANA
FIRENZE

Biogene- Biobank of biological material from patients affected by genetic diseases
Azienda Ospedaliero Universitaria Careggi
S.O.D. Diagnostica Genetica

PAISES BAJOS (LOS)

Groningen
GRONINGEN

L1CAM Mutation Database
UMCG - Universitair Medisch Centrum Groningen
Laboratorium DNA Diagnostiek

PAISES BAJOS (LOS)

Zuid-Holland
ROTTERDAM

Biobank Frontotemporal Dementia Erasmus MC (DNA/RNA/plasma/serum/tissue)
Erasmus MC - Erasmus Medisch Centrum
Alzheimercentrum Erasmus MC

REINO UNIDO (EL)

Greater Manchester
SALFORD

EuroMyositis registry
Hope Hospital, University of Manchester
The University of Manchester Rheumatic Diseases Centre

REINO UNIDO (EL)

Surrey
SUTTON

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE UPON TYNE

UK and Ireland Spinal muscular atrophy (SMA) patient registry (part of the TREAT-NMD network)
Newcastle University
John Walton Muscular Dystrophy Research Centre, Institute for Genetic Medicine

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE UPON TYNE

UK and Ireland Spinal muscular atrophy (SMA) patient registry (part of the TREAT-NMD network)
Newcastle upon Tyne Hospitals NHS Trust
John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine

REPUBLICA CHECA (LA)

South Moravia
BRNO

Spinal muscular atrophy patient registry in the Czech Republic - part of the TREAT-NMD network
University hospital Brno
Institute of Biostatistics and Analyses

SUECIA

Region Skåne
LUND

DKC1base: Mutation registry for Hoyeraal-Hreidarsson syndrome and dyskeratosis congenita
Lund University
Department of Experimental Medical Science

SUECIA

Region Skåne
LUND

SUECIA

Region Västerbotten
UMEÅ

Swedish Registry for Familial Amyloid Polyneuropathy
University Hospital of Umeå
Department of Medicine

SUIZA

Suisse Alémanique
BASEL

Swiss Registry for Neuromuscular Disorders
Universitäts-Kinderspital beider Basel UKBB
Die Abteilung für Neuro- und Entwicklungspädiatrie

SUIZA

Suisse Alémanique
BERN

Swiss Registry for Neuromuscular Disorders
Institute of Social and Preventive Medicine (ISPM)

TURQUIA

TURKEY
ANKARA

Duchenne and Becker muscular dystrophy and spinal muscular dystrophy patient registries in Turkey - contributes to the TREAT-NMD network
Hacettepe University Faculty of Medicine
Department of physical therapy and rehabilitation

UCRANIA

UKRAINE
KHARKIV

Spinal muscular atrophy patient registry in Ukraine - part of the TREAT-NMD network
Academy of medical science of Ukraine
Institute of Neurology, Psychiatry and Narcology

ALEMANIA

Bayern
MÜNCHEN

ALEMANIA

Bayern
MÜNCHEN

German DM registry: Patient registry for myotonic dystrophy (DM)
Friedrich-Baur-Institut
TREAT-NMD-Patientenregister

ALEMANIA

Hessen
FRANKFURT AM MAIN

Ataxia-Telangiectasia patient registry - contributes to the ESID Database
Klinikum der Johann Wolfgang Goethe-Universität Frankfurt
Schwerpunkt Allergologie, Pneumologie und Mukoviszidose

ALEMANIA

Hessen
MARBURG

German national case collection of familial pancreatic cancer
Universitätsklinikum Gießen und Marburg GmbH, Standort Marburg
Klinik für Visceral- Thorax- und Gefäßchirurgie

AUSTRALIA

Western Australia
CRAWLEY

Nemaline myopathy variant database
University of Western Australia and Western
Centre for MedicalResearch

BELGICA

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

EUNEFRON: registry of the European network for the study of orphan nephropathies
Cliniques universitaires Saint-Luc - UCLouvain
Laboratory of Nephrology

ESPAÑA

Asturias
OVIEDO

Financiado por un miembro del IRDiRCRenalTube: Base de datos de pacientes con tubulopatías primarias
Hospital Universitario Central de Asturias
Servicio de Pediatría

ESPAÑA

Cataluña
BARCELONA

Financiado por un miembro del IRDiRCEUROMAC: Registro de pacientes afectados por la enfermedad de McArdle
Vall d'Hebron Institut de Recerca VHIR
Grupo de investigación en patología neuromuscular y mitocondrial

FRANCIA

BRETAGNE
RENNES

French cohort of rhombencephalosynapsis
CHU de Rennes - Hôpital Sud
Service de génétique clinique

FRANCIA

BRETAGNE
RENNES

French biological collection of rhombencephalosynapsis
CHU de Rennes - Hôpital Sud
Service de génétique clinique

FRANCIA

ILE-DE-FRANCE
CRÉTEIL

DM Scope: Myotonic dystrophy patient registry in France - part of the TREAT-NMD network
Hôpitaux Universitaires Henri Mondor
Service de neurologie

FRANCIA

ILE-DE-FRANCE
PARIS

French cohort in genetic microcephalies
CHU Paris - Hôpital Robert Debré
UF de Génétique clinique

FRANCIA

ILE-DE-FRANCE
PARIS

CoF-AT study: a French cohort on ataxia-telangiectasia
CLCC Institut Curie
Cancer et génome: bioinformatique, biostatistiques et épidémiologie d'un système complexe

FRANCIA

ILE-DE-FRANCE
PARIS

CoF-AT study: a French cohort on ataxia-telangiectasia
CLCC Institut Curie
Service de Génétique

FRANCIA

ILE-DE-FRANCE
PARIS

UMD LMNA (Lamin A/C) mutations database
Institut de Myologie - Hôpital Pitié-Salpêtrière
Centre de Recherche en Myologie

FRANCIA

OCCITANIE
MONTPELLIER

French cohort of focal dystonia famillies
IURC - Institut Universitaire de Recherche Clinique
Laboratoire de génétique moléculaire

ITALIA

LAZIO
ROMA

RIAT: Ataxia teleangiectasia Italian registry
A.O. S. Andrea
Servizio di Genetica Medica

ITALIA

LAZIO
ROMA

V-RIAT: variant Ataxia telangiectasia Italian registry
A.O. S. Andrea
Servizio di Genetica Medica

ITALIA

LAZIO
ROMA

Financiado por un miembro del IRDiRCTelethon-UILDM registry CMD (Congenital Muscular Dystrophy) - contributes to european Treat-NMD network
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
U.O.C. Neuropsichiatria Infantile

ITALIA

LOMBARDIA
MILANO

INNCB MG Registry
Fondazione IRCCS Istituto Neurologico "Carlo Besta"
U.O. Neurologia IV - Malattie Neuromuscolari e Neuroimmunologia

ITALIA

LOMBARDIA
SAN DONATO MILANESE

Italian registry of myotonic dystrophies
IRCCS Policlinico San Donato
U.O. di Neurologia - Centro per lo Studio delle Malattie Neuromuscolari

REINO UNIDO (EL)

Greater London
LONDON

UK and Ireland Juvenile Dermatomyositis Cohort Biomarker Study and Repository
GOSH NHS Foundatin Trust
Juvenile Dermatomyositis Research Centre

REINO UNIDO (EL)

Greater London
LONDON

REINO UNIDO (EL)

Greater London
LONDON

UK and Ireland Juvenile Dermatomyositis Cohort Biomarker Study and Repository
The Institute of Child Health & The Division of Medicine, UCL
The Institute of Child Health & The Division of Medicine

REINO UNIDO (EL)

Merseyside
LIVERPOOL

UK and Ireland Juvenile Dermatomyositis Cohort Biomarker Study and Repository
Alder Hey Children's Hospital
Department of Rheumatology

REINO UNIDO (EL)

South Glamorgan
CARDIFF

Myotonic dystrophy patient registry in United Kingdom - part of the TREAT-NMD network
University Hospital of Wales
Institute of Medical Genetics

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE UPON TYNE

Myotonic dystrophy patient registry in United Kingdom - part of the TREAT-NMD network
Newcastle upon Tyne Hospitals NHS Trust
John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine

SUECIA

Region Skåne
LUND

MRE11Abase: Mutation registry for Ataxia-telangiectasia-like disorder (ATLD)
Lund University
Department of Experimental Medical Science

ALEMANIA

Bayern
MÜNCHEN

German FSHD registry: Patient registry for Facioscapulohumeral dystrophy (FSHD)
Friedrich-Baur-Institut
TREAT-NMD-Patientenregister

ALEMANIA

Nordrhein-Westfalen
MÜNSTER

Nephronophthisis registry for patients in germany, austria and switzerland
KfH Kuratorium für Dialyse und Nierentransplantation e.V.
KfH-Nierenzentrum für Kinder und Jugendliche

ALEMANIA

Nordrhein-Westfalen
MÜNSTER

Nephronophthisis registry for patients in germany, austria and switzerland
Universitätsklinikum Münster
Klinik für Kinder- und Jugendmedizin - Allgemeine Pädiatrie

AUSTRALIA

New South Wales
MARRICKVILLE

DuchenneConnect Australia patient registry
Save Our Sons Duchenne Foundation

ESPAÑA

Cataluña
BARCELONA

The Connexin-deafness mutations database
Centro de Regulación Genómica
Programa Genes y Enfermedad

ESTADOS UNIDOS

Washington
SEATTLE

FRANCIA

ILE-DE-FRANCE
PARIS

Duchenne and Becker muscular dystrophy patient registry in France - part of the TREAT-NMD network
CHU Paris Centre - Hôpital Cochin, Site Cochin
Service de génétique et biologie moléculaires

FRANCIA

ILE-DE-FRANCE
PARIS

Financiado por un miembro del IRDiRCLaminopathies and emerinopathies patient registry
Institut de Myologie - Hôpital Pitié-Salpêtrière
Équipe "Génétique, Physiopathologie & approches thérapeutiques des maladies du muscle"

FRANCIA

OCCITANIE
MONTPELLIER

Duchenne and Becker muscular dystrophy patient registry in France - part of the TREAT-NMD network
IURC - Institut Universitaire de Recherche Clinique
Laboratoire de génétique moléculaire

FRANCIA

PAYS DE LA LOIRE
ANGERS

eOPA1: mutations registry of OPA1 gene (Optic atrophy 1)
CHU d'Angers
UF de Génétique Moléculaire

FRANCIA

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

UMD-DYSF, a locus-specific database for the compilation and interactive analysis of mutations in the Dysferlin gene.
Faculté de Médecine de la Timone
Centre d'enseignement et de recherche en génétique médicale - INSERM UMR S910

FRANCIA

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Financiado por un miembro del IRDiRCFrench National FSHD Registry
Faculté de Médecine de la Timone
Centre d'enseignement et de recherche en génétique médicale - INSERM UMR S910

HUNGRIA

Közép-Magyarország
BUDAPEST

DMD registry - Hungary - contributes to the TREAT-NMD network
National Institute of Environmental Health
Department of Molecular Genetics and Diagnostics

ITALIA

EMILIA ROMAGNA
MODENA

ITALIA

LAZIO
ROMA

DMD / BMD Italy Patient Registry
Parent Project - ONLUS

ITALIA

LOMBARDIA
MILANO

Telethon-UILDM registry LGMD (Limb Girdle Muscular Dystrophy) - contributes to european Treat-NMD network
Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico
Dipartimento di Scienze Neurologiche

PAISES BAJOS (LOS)

Gelderland
NIJMEGEN

FSHD registry
Radboudumc - Radboud universitair medisch centrum
Afdeling Neurologie

PAISES BAJOS (LOS)

Zuid-Holland
LEIDEN

PORTUGAL

NORTE
PORTO

Duchenne and Becker muscular dystrophy patient registry in Portugal - contributes to the TREAT-NMD network
CGMJM - Centro de Genética Médica Jacinto Magalhães
Centro de Genética Médica Jacinto Magalhães

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE UPON TYNE

The MTM and CNM Registry - The Myotubular and Centronuclear Myopathy Patient Registry
Newcastle University
John Walton Muscular Dystrophy Research Centre, Institute for Genetic Medicine

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE UPON TYNE

The Global Registry for COL6-related dystrophies
Newcastle University
John Walton Muscular Dystrophy Research Centre, Institute for Genetic Medicine

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE UPON TYNE

The MTM and CNM Registry - The Myotubular and Centronuclear Myopathy Patient Registry
Newcastle upon Tyne Hospitals NHS Trust
John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine

REINO UNIDO (EL)

Tyne & Wear
NEWCASTLE UPON TYNE

UK facioscapulohumeral muscular dystrophy patient registry (part of the TREAT-NMD network)
Newcastle upon Tyne Hospitals NHS Trust
John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine

REPUBLICA CHECA (LA)

South Moravia
BRNO

ALEMANIA

Hamburg
HAMBURG

Financiado por un miembro del IRDiRCPompe Disease Registry - DE
UKE - Universitätsklinikum Hamburg-Eppendorf
Klinik und Poliklinik für Kinder- und Jugendmedizin

ESPAÑA

Cataluña
BARCELONA

ESPAÑA

Comunidad Valenciana
VALENCIA

Registro español de pacientes con distrofia muscular tipo Duchenne - parte de la red TREAT-NMD
IIS La Fe - Instituto de Investigación Sanitaria La Fe
Grupo de investigación en biomedicina molecular, celular y genómica

ESPAÑA

Madrid
MADRID

Registro español de pacientes con la enfermedad de McArdle
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares

ESPAÑA

Madrid
VILLAVICIOSA DE ODÓN

Registro español de pacientes con la enfermedad de McArdle
Universidad Europea de Madrid. Facultad de Ciencias de la Salud
Laboratorio de Fisiología del Ejercicio

FRANCIA

ILE-DE-FRANCE
PARIS

UMD DMD (Dystrophin) mutations database
CHU Paris Centre - Hôpital Cochin, Site Cochin
Service de génétique et biologie moléculaires

FRANCIA

ILE-DE-FRANCE
PARIS

UMD EMD (Emerin) mutations database
Institut de Myologie - Hôpital Pitié-Salpêtrière
Centre de Recherche en Myologie

FRANCIA

ILE-DE-FRANCE
PARIS

French certified registry of glycogen storage disease type 2
Institut de Myologie - Hôpital Pitié-Salpêtrière
Unité clinique de pathologie neuromusculaire

FRANCIA

OCCITANIE
MONTPELLIER

UMD DMD (Dystrophin) mutations database
IURC - Institut Universitaire de Recherche Clinique
Laboratoire de génétique moléculaire

ITALIA

LOMBARDIA
MILANO

Financiado por un miembro del IRDiRCBank of cells, tissues and DNA from patients with neuromuscular diseases (EuroBioBank partner)
Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
Laboratorio di Biologia della Cellula Muscolare

PAISES BAJOS (LOS)

Noord-Holland
NAARDEN

The intenational Pompe registry
Genzyme Europe B.V.

REINO UNIDO (EL)

Essex
LONDON

North Star database
Great Ormond Street Hospital
Dubowitz Neuromuscular Centre

SUECIA

Region Skåne
LUND

TAZbase: Mutation registry for Barth syndrome
Lund University
Department of Experimental Medical Science

SUIZA

Suisse Alémanique
BERN

Financiado por un miembro del IRDiRCSwiss Pompe Registry
Inselspital Universitätsspital
Centre for Neuromuscular Diseases

Redes de registos y biobancos

ALEMANIA

Bayern
MÜNCHEN

BNE: BRAINNET EUROPE II (Network of European Brain and Tissue Banks for Clinical and Basic Neuroscience)
  • Zentrum für Neuropathologie und Prionforschung (ZNP)
  • Zentrum für Neuropathologie und Prionforschung der LMU München
  • REINO UNIDO (EL)

    Tyne & Wear
    NEWCASTLE UPON TYNE

    Financiado por un miembro del IRDiRCTREAT-NMD: Accelerating Treatments for Neuromuscular Diseases (registries)
  • Newcastle upon Tyne Hospitals NHS Trust
  • John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine
  • ALEMANIA

    Baden-Württemberg
    HEIDELBERG

    iNTD Network - International Working Group on Neurotransmitter Related Disorders
  • Dietmar-Hopp-Stoffwechselzentrum
  • Klinik für Kinderheilkunde I - Stoffwechsellabor
  • PAISES BAJOS (LOS)

    Noord-Holland
    AMSTERDAM

    Financiado por un miembro del IRDiRCE-HOD - European network and registry for homocystinurias and methylation defects
  • Amsterdam UMC, locatie VUmc
  • Afdeling Interne Geneeskunde
  • REINO UNIDO (EL)

    South Yorkshire
    SHEFFIELD

    Financiado por un miembro del IRDiRCEUROWILSON: European network on Wilson disease (registries)
  • The Sheffield Children's Hospital
  • Sheffield Children's Hospital (Division of Child Health)
  • FRANCIA

    PROVENCE-ALPES-COTE D'AZUR
    MARSEILLE

    EURORETT: European network on Rett syndrome (registry)
  • Faculté de Médecine de la Timone
  • Centre d'enseignement et de recherche en génétique médicale - INSERM UMR S910
  • REINO UNIDO (EL)

    Antrim and Newtownabbey
    NEWTOWNABBEY