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Projetos de investigação encerrados = Financiado por um membro do IRDiRC = Membro de uma ERN =

Projetos de investigação

CANADA

Québec
MONTRÉAL

Financiado por um membro do IRDiRCUnraveling the molecular basis of novel forms of hypomyelinating leukodystrophies
Montreal Children's Hospital Research Institute - McGill University
Pediatric Neurodegenerative Laboratory

ALEMANHA

Baden-Württemberg
TÜBINGEN

LEUKO-Expert: Diagnosis Support for the Rare Disease Family Leukodystrophy
Hertie-Institut für klinische Hirnforschung (HIH)
Abteilung Neurologie mit Schwerpunkt neurodegenerative Erkrankungen

ALEMANHA

Nordrhein-Westfalen
AACHEN

LEUKO-Expert: Diagnosis Support for the Rare Disease Family Leukodystrophy
Universitätsklinikum Aachen
Klinik für Neurologie

ALEMANHA

Nordrhein-Westfalen
BONN

ALEMANHA

Sachsen
LEIPZIG

LEUKO-Expert: Diagnosis Support for the Rare Disease Family Leukodystrophy
Universitätsklinikum Leipzig AöR
Klinik und Poliklinik für Neurologie

ALEMANHA

Sachsen
MITTWEIDA

LEUKO-Expert: Diagnosis Support for the Rare Disease Family Leukodystrophy
Hochschule Mittweida
Datenbank Gruppe - Prof. Dr. T. Kirsten

CANADA

Québec
MONTRÉAL

Clinical, radiological and genetic characterization of new forms of leukodystrophies
Montreal Children's Hospital Research Institute - McGill University
Pediatric Neurodegenerative Laboratory

FRANCA

ILE-DE-FRANCE
PARIS

Financiado por um membro do IRDiRCNG4LEUKO: Exploring neuron-glia interactions in leukodystrophies using human iPSC-based models: implication for therapy - FR
Institut de Psychiatrie et Neurosciences Paris (IPNP), Inserm UMR_S 1266
Equipe Interactions entre neurones et oligodendroglies dans la myélinisation et la réparation de la myéline

ITALIA

LOMBARDIA
MILANO

Financiado por um membro do IRDiRCNG4LEUKO: Exploring neuron-glia interactions in leukodystrophies using human iPSC-based models: implication for therapy - IT
Istituto San Raffaele Telethon per la Terapia Genica - TIGET
Istituto San Raffaele Telethon per la Terapia Genica

ESPANHA

Cataluña
BARCELONA

ESPANHA

Cataluña
BARCELONA

Igenco: In-Depth genomics and cross-omics analysis for undiagnosed rare diseases on a user-friendly collaborative platform
ISGlobal - Instituto de Salud Global de Barcelona
Programa de investigación en Enfermedades no transmisibles y medio ambiente

ITALIA

LAZIO
ROMA

Financiado por um membro do IRDiRCDiverse rare diseases caused by functional dysregulation of Rho GTPase-related proteins
ISS - Istituto Superiore di Sanità
Centro Nazionale Malattie Rare

CANADA

Colombie-Britannique
VICTORIA

CANADA

Ontario
TORONTO

ESPANHA

Cataluña
BARCELONA

Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Centro de Regulación Genómica
Archivo europeo de genomas y fenomas del CRG

ESPANHA

Cataluña
BARCELONA

ESPANHA

Cataluña
BARCELONA

ESPANHA

Cataluña
BARCELONA

ESPANHA

Cataluña
ESPLUGUES DE LLOBREGAT

ESPANHA

Cataluña
L'HOSPITALET DE LLOBREGAT

Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Universitari de Bellvitge
Unidad de Genética Molecular

ESPANHA

Madrid
MADRID

Financiado por um membro do IRDiRCIdentification of new genes causing rare diseases in pediatric patients, searching of genetic pharmacological targets, and drugs discovery, the steps for a personalized medicine
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares

Projetos de investigação multicêntricos