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223 Ergebnis(se)
Abgeschlossene Forschungsprojekte = Förderung durch ein IRDiRC-Mitglied =
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Forschungsprojekt(e)

County Dublin
DUBLIN
Establishment of a scalable semantic data architecture for study of chronic disease
Trinity College Dublin
ADAPT Centre

County Dublin
DUBLIN
Ensemble averaging for complex disease prediction in the large p small n domain from multiple data sources
Trinity College Dublin
School of Computer Science and Statistcs - O'Reilly Institute

Baden-Württemberg
FREIBURG
SFB 1140 (KIDGEM) : Identifizierung von TULP3-Mutationen bei Patienten mit zystischen Nierenerkrankungen und verwandten Ziliopathien
Zentrum für Klinische Forschung am Universitätsklinikum Freiburg
Nephro Lab

Baden-Württemberg
HEIDELBERG
NEOCYST: Multidisziplinäres Netzwerk zur Erforschung der Pathogenese, der klinischen Präsentation und der Prognose hereditärer zystischer Nierenerkrankungen im Kindesalter (Verbundprojekt SE)
Zentrum für Kinder- und Jugendmedizin des Universitätsklinikums Heidelberg
Klinik für Kinderheilkunde I - Sektion Pädiatrische Nephrologie

Niedersachsen
HANNOVER
Charakterisierung von drei mit kongenitalen Anomalien der Nieren und ableitenden Harnwege (CAKUT) assoziierten Kandidatengenen und von deren Varianten mittels in vitro und in vivo Modellsystemen
Medizinische Hochschule Hannover
Institut für Humangenetik

Nordrhein-Westfalen
ESSEN
NEOCYST: Multidisziplinäres Netzwerk zur Erforschung der Pathogenese, der klinischen Präsentation und der Prognose hereditärer zystischer Nierenerkrankungen im Kindesalter (Verbundprojekt SE)
Universitätsklinikum Essen
Klinik für Kinderheilkunde II

Nordrhein-Westfalen
KÖLN
NEOCYST: Multidisziplinäres Netzwerk zur Erforschung der Pathogenese, der klinischen Präsentation und der Prognose hereditärer zystischer Nierenerkrankungen im Kindesalter (Verbundprojekt SE)
Universitätsklinikum Köln
Pädiatrische Nephrologie, Immunologie und Hypertensiologie

Nordrhein-Westfalen
MÜNSTER
NEOCYST: Multidisziplinäres Netzwerk zur Erforschung der Pathogenese, der klinischen Präsentation und der Prognose hereditärer zystischer Nierenerkrankungen im Kindesalter (Verbundprojekt SE)
KfH Kuratorium für Dialyse und Nierentransplantation e.V.
KfH-Nierenzentrum für Kinder und Jugendliche

Rheinland-Pfalz
MAINZ
NEOCYST: Multidisziplinäres Netzwerk zur Erforschung der Pathogenese, der klinischen Präsentation und der Prognose hereditärer zystischer Nierenerkrankungen im Kindesalter (Verbundprojekt SE)
Limbach Genetics GmbH
Medizinische Genetik Mainz - Limbach Genetics

ILE-DE-FRANCE
PARIS
Predisposition factors in hemolytic uremic syndrome, atypical form, and in thrombotic microangiopathies
AP-HP. Centre - Université de Paris - HEGP Hôpital Européen Georges Pompidou
Laboratoire d'Immunologie biologique

ILE-DE-FRANCE
PARIS
TRAJHISTORY project: assessing single cell TRAJectories and alterations of cell communication and tissue HISTOry to get causal insights into rare and catastrophic glomerular disease
PARCC - Paris-Centre de recherche Cardiovasculaire (U970)
Centre de Recherche Cardiovasculaire

KOREA, REPUBLIC OF
KOREA
Factors associated with chronic and severe status of rare disease and health-related quality of life among rare disease patients
Korea National Institute of Health

KOREA, REPUBLIC OF
KOREA
Integrative study of epigenetic variations in rare diseases
Korea National Institute of Health

KOREA, REPUBLIC OF
SEOUL
Establishment and operation of the clinical research network for rare glomerular diseases
Yonsei University College of Medicine

South Dakota
SIOUX FALLS
The molecular regulators of kidney collecting duct differentiation and maintenance
Sanford Research
Surendran Lab

ANTWERPEN
EDEGEM (ANTWERPEN)
Empowering Families through Technology: a mobile-health project to reduce the TAND identification and treatment gap (TANDem)
Antwerp University Hospital - UZA
Pediatric neurology/Kinderneurologie

ANTWERPEN
EDEGEM (ANTWERPEN)
GAGA: Identification of Gait Disorders in Children, Adolescents and Young Adults With Rare Genetic Diseases
Antwerp University Hospital - UZA
Pediatric neurology/Kinderneurologie

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS
EUNEFRON: rare disorders of the distal convoluted tubule (WP4)
Cliniques universitaires Saint-Luc - UCLouvain
Laboratory of Nephrology

Baden-Württemberg
FREIBURG
Die Rolle von CCL2 in der Nephronophthise und der autosomal dominanten polyzystischen Nierenerkrankung (ADPKD)
Zentrum für Klinische Forschung am Universitätsklinikum Freiburg
Nephro Lab

Baden-Württemberg
FREIBURG
Charakterisierung des DZIP1L-Proteins im Bereich der ziliären Transitionszone und seine Wechselwirkungen mit anderen Zystennieren-Proteinen
Zentrum für Klinische Forschung am Universitätsklinikum Freiburg
Nephro Lab

Bayern
MÜNCHEN
Die Rolle Kinase-gekoppelter TRP-Kanäle in der Mg2+-Homöostase: Von Mausmodellen zu menschlicher Erkrankung (TRR 152: P15)
Walther-Straub-Institut für Pharmakologie und Toxikologie der LMU München
Walther-Straub-Institut für Pharmakologie und Toxikologie

Berlin
BERLIN
FIGHT-CNNM2: Verbesserung von Diagnostik und Verständnis der Mechanismen von Hypomagnesiämie bei Patienten mit CNNM2-Mutationen
Charité - Universitätsmedizin Berlin (CVK)
Klinik für Pädiatrie mit Schwerpunkt Gastroenterologie, Nephrologie und Stoffwechselmedizin

Nordrhein-Westfalen
KÖLN
Das deutsche ADPKD-Tolvaptan-Behandlungsregister: Prospektive, beobachtende, multizentrische Studie von Patienten, die an ADPKD leiden und für eine Tolvaptan-Behandlung in Frage kommen
Universitätsklinikum Köln
Klinik II für Innere Medizin - Nephrologie, Rheumatologie, Diabetologie und allgemeine Innere Medizin

Nordrhein-Westfalen
MÜNSTER
Immunzellprofile im Blut bei Kindern, Jugendlichen und Erwachsenen mit Tuberöse Sklerose Komplex Erkrankung und deren Korrelation mit Organmanifestationen und Therapieansprechen auf eine Immuntherapie mit mTOR Inhibitoren
Universitätsklinikum Münster
Klinik für Neurologie mit Institut für Translationale Neurologie

Sachsen
LEIPZIG
Genetische Determinanten der Nierensteinbildung bei ADPKD
Universitätsklinikum Leipzig AöR
Klinik und Poliklinik für Endokrinologie, Nephrologie, Rheumatologie

AUVERGNE-RHONE-ALPES
GRENOBLE
Physiopathological studies of Lowe's syndrome and Dent's disease, two clinical entities with common molecular basis?
CHU Grenoble Alpes
Laboratoire de Génétique Moléculaire: maladies héréditaires et oncologie

ILE-DE-FRANCE
PARIS
EUNEFRON: rare disorders of the distal convoluted tubule (WP4)
AP-HP. Centre - Université de Paris - HEGP Hôpital Européen Georges Pompidou
Service de génétique

ILE-DE-FRANCE
PARIS
Pheno2Geno: Regulation of NKCC2 and NCC by Protein-Protein interactions: From salt losing tubulopathies to salt sensitive hypertension - FR
Centre de Recherches des Cordeliers (CRC)
Equipe "Métabolisme et Physiologie Rénale"

ILE-DE-FRANCE
PARIS
Identification of New Molecular Mechanisms involved in Bartter Syndrome
Centre de Recherches des Cordeliers (CRC)
Centre de Recherche des Cordeliers (CRC) - INSERM UMRS 1138

ILE-DE-FRANCE
PARIS
Whole Genome Sequencing to Unravel the Genetic Mechanisms of PLA2R-Associated Membranous Nephropathy
Groupe hospitalier AP-HP.6 - Hôpital Tenon
INSERM UMRS 1155 "Des maladies rénales aux maladies fréquentes, remodelage et réparation"

ILE-DE-FRANCE
PARIS
Study of the rupture of tubular homeostasis in polycystic kidney disease
Hôpital Necker-Enfants Malades
Néphropathies héréditaires et rein en développement

OCCITANIE
MONTPELLIER
Determination of the three-dimensional structure of the active and inactive conformations of the vasopressin V2 receptor StrainV2
IGF - Institut de Génomique Fonctionnelle
Département Neurosciences

CAMPANIA
NAPOLI
Role of phosphoinositide metabolism in the structure and function of the Golgi complex and in the pathogenesis of Lowe syndrome
TIGEM - Telethon Institute of Genetics and Medicine
Laboratorio di Ricerca

Gelderland
NIJMEGEN
The magnesium journey through the renal cell: how to get out?
Radboudumc - Radboud universitair medisch centrum
Afdeling Fysiologie

Gelderland
NIJMEGEN
FIGHT-CNNM2: For Improving diagnostics and Grasping the disease mechanisms of rare Hypomagnesemia in paTients with CNNM2 mutations - NL
Radboudumc - Radboud universitair medisch centrum
Afdeling Fysiologie

Gelderland
NIJMEGEN
TREATCilia: Novel Therapeutic Avenues for dynein-related Ciliopathies
Radboudumc - Radboud universitair medisch centrum
Afdeling Genetica

Østlandet
OSLO
Effectiveness and safety of mTOR-inhibitor in patients with tuberous sclerosis complex
Oslo University Hospital, Ullevaal
NevSom - Nasjonalt kompetansesenter for nevroutviklingsforstyrrelser og hypersomier

WIEN
ADDRESS: NOT PROVIDED - AT
JINARC PASS: A 9-year, Multicentre, Non-interventional, Post-authorisation Safety Study for Patients Prescribed JINARC® for Autosomal Dominant Polycystic Kidney Disease - AT
Institution: Information not provided - AT

Region Skåne
LUND
Bacterial virulence factors, innate immunity and prothrombotic mechanisms in renal disease
Lund University
Department of Clinical Sciences - Division of Pediatrics

Region Stockholm
STOCKHOLM
Understanding Genetic Mechanisms in Disorders and Development of Diagostic Methods
Karolinska Institutet - Solna
Department of Molecular Medicine and Surgery (MMK)

Region Örebro län
ÖREBRO
Study on cognitive hearing sciences (Linnéus HEAD) in Ushers, Alström syndrome, CHARGE and other syndromic deafness disorders
Örebro University Hospital
Department of Audiology/ Audiological Clinical Research Centre

Suisse Alémanique
BERN
Thrombotic thrombocytopenic purpura - role of ADAMTS13 and long-term outcome
Universitätsspital Inselspital
Department of Hematology and Central Hematology Laboratory

Canarias
LAS PALMAS DE GRAN CANARIA
Investigation of therapeutic strategies for Dent-1 disease and adaptation of RenalTube to the needs of patients with primary tubulopathies
Hospital Universitario de Gran Canaria Dr. Negrín
FIISC: Fundación Canaria Instituto de Investigación Sanitaria de Canarias

Cataluña
BARCELONA
Therapeutical strategies for cystinuria
IRB Barcelona - Instituto de Investigación Biomédica
Transportadores de aminoácidos y enfermedad

Cataluña
BARCELONA
Deciphering the mechanisms of PLA2R-specific B-cell autoimmunity in primary membranous nephropathy (PMN) (BCELL-MEM)
Vall d'Hebron Institut de Recerca VHIR
Grupo de investigación en nefrología y trasplante renal

Cataluña
L'HOSPITALET DE LLOBREGAT
Cystinuria: Validation of a new cystine lithiasis biomarker in patients and design of a new treatment based on cystine lithiasis modulators identified in mouse models
IDIBELL - Instituto de Investigación Biomédica de Bellvitge
Instituto de Investigación Biomédica de Bellvitge

Cataluña
MARTORELL
FIGHT-CNNM2: For Improving diagnostics and Grasping the disease mechanisms of rare Hypomagnesemia in patients with CNNM2 mutations - ES
Asociación para la información y la investigación de la Hipomagnesemia Familiar

Comunidad Valenciana
VALENCIA
Therapeutical strategies for cystinuria
INCLIVA - Facultad de Medicina de la Universidad de Valencia
Grupo de investigación en fisiopatología celular y orgánica del estrés oxidativo

Galicia
VIGO
Molecular mechanisms in ciliopathies
Universidade de Vigo
Grupo de Enfermedades raras

País Vasco
BARAKALDO
FIGHT-CNNM2: For Improving diagnostics and Grasping the disease mechanisms of rare Hypomagnesemia in patients with CNNM2 mutations - ES
Hospital Universitario Cruces
Unidad de Trastornos Congénitos del Metabolismo

País Vasco
DERIO
FIGHT-CNNM2: For Improving diagnostics and Grasping the disease mechanisms of rare Hypomagnesemia in patients with CNNM2 mutations - ES
Centro de Investigación Cooperativa en Biociencias (CIC bioGUNE)
Liver Disease Lab

País Vasco
ÁLAVA
Application of new technologies in rare disorders: artificial intelligence and next generation sequencing in inactivating PTH/PTHrP signalling disorders
Instituto de Investigación Sanitaria Bioaraba

Washington
ADDRESS: NOT PROVIDED - US
Human biochemical genetics
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Mechanisms of retinal degeneration in inherited diseases
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Mechanotransduction and the regulation of skeletal muscle mass
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Elucidating the neuropathophysiology of tsc using genetically engineered human neurons
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Zfp423 mechanisms in joubert syndrome and related disorders
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Filamin a in tsc
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Mechanisms of synapse remodeling in tsc
Institution: Information not provided - US

West Midlands
BIRMINGHAM
EURO-WABB: EURO-Rare Diabetes Project (coordination)
Birmingham Children's Hospital NHS Foundation Trust
Diabetes Unit

VLAAMS BRABANT
LEUVEN
Molecular and functional pathogenesis in NF1 and related diseases
UZ Leuven - Campus Gasthuisberg
Centrum Menselijke Erfelijkheid - UZ Leuven

Baden-Württemberg
FREIBURG
Eine prospektive, internationale, multizentrische Verlaufbeobachtungsstudie bei Patienten mit kombiniertem T-Zell Immundefekt (profound combined immunodeficiency : P-CID)
CCI am Universitätsklinikum Freiburg
Centrum für Chronische Immundefizienz

Bayern
ERLANGEN
Pathogenese der autosomal dominanten-tubulointerstitiellen Nierenerkrankung (SFB 1350: Tubulussystem und Interstitium der Niere: (Patho-)Physiologie und Crosstalk)
Internistisches Zentrum des Universitätsklinikums Erlangen
Medizinische Klinik 4 - Nephrologie und Hypertensiologie

Berlin
BERLIN
CLC Cl-Kanäle und Transporter in grundlegenden zellulären Prozessen und pathologischen Zuständen
Leibniz-Institut für Molekulare Pharmakologie
Department Physiology and Pathology of Ion Transport

Berlin
BERLIN
Molekulare Genetik der autosomal-dominanten Hypertonie mit Brachydaktylie Typ E
Max-Delbrück-Centrum für Molekulare Medizin
AG Luft - Genetik und Pathophysiologie des Herz - Kreislaufsystems

Mecklenburg-Vorpommern
GREIFSWALD
Mutationsspektrum und klinische Symptomatik bei Patienten mit genetisch bedingten Hämostasestörungen
Institut für Humangenetik der Universitätsmedizin Greifswald
Institut für Humangenetik

Niedersachsen
GÖTTINGEN
Europäisches Alport-Therapieregister
Universitätsmedizin Göttingen
Klinik für Nephrologie und Rheumatologie

Niedersachsen
GÖTTINGEN
Bedeutung der Interaktion von Schlitzmembran, Podozyt und glomerulärer Basalmembran bei der Pathogenese von glomerulären Nierenerkrankungen wie dem Alport Syndrom
Universitätsmedizin Göttingen
Klinik für Nephrologie und Rheumatologie

Nordrhein-Westfalen
BAD OEYNHAUSEN
Molekularbiologische Diagnostik und Pathobiochemie des Pseudoxanthoma elasticum
Ruhr-Universität Bochum
Institut für Laboratoriums- und Transfusionsmedizin

Nordrhein-Westfalen
BONN
Luto-Studie: Systematische Untersuchung der molekularen Ursachen bei Kongenitalen Uro-Rektalen Malformationen für Probanden und Angehörige mit LUTO (Lower Urinary Tract Obstruction)
Universitätsklinikum Bonn (AöR)
Institut für Humangenetik

Schleswig-Holstein
LÜBECK
DSDCare: Standardisierte Zentren-zentrierte Versorgung von DSD (Differences in Sex-Development) über die Lebensspanne
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Hormonzentrum für Kinder und Jugendliche - Lübeck

Finland
TURKU
Clinical research study on neurofibromatosis type 1 in Finland
University of Turku
Institute of Biomedicine

AUVERGNE-RHONE-ALPES
PRAGUE
Neurofibromatosis type 1 Disease Model
Faculty of Medicine and University Hospital Motol
Department of Pediatrics

AUVERGNE-RHONE-ALPES
PRAGUE
Role on Nonmuscle Myosin II in membrane trafficking and organ function
Faculty of Medicine and University Hospital Motol
Department of Pediatrics

GRAND-EST
STRASBOURG
Bernard-Soulier Syndrome and MYH9 associated diseases: study of blood platelets anomalies and of the thrombopoïesis, correction by genetic therapy
Établissement Français du Sang - Grand Est
UR U311 - Biologie et pharmacologie de l'hémostase et de la thrombose

ILE-DE-FRANCE
PARIS
Implementation of non-invasive prenatal diagnosis of rare and severe monogenic diseases
AP-HP.Centre - Université de Paris - Hôpital Cochin
Service de Médecine Génomique des Maladies de Système et d'Organe

ILE-DE-FRANCE
PARIS
Molecular signature of convertase activation in complement-dependent glomerulopathies
Centre de Recherches des Cordeliers (CRC)
Centre de Recherche des Cordeliers (CRC) - INSERM UMRS 1138

ILE-DE-FRANCE
PARIS
Constitutive hematologic diseases: clinical and therapeutic research, molecular biology
GHU AP-HP Nord. Université de Paris - Hôpital Saint-Louis
Service d'hématologie pédiatrique

OCCITANIE
TOULOUSE
Structure-function relationship of the TSH receptor and of the related receptors
CHU de Toulouse - Hôpital Rangueil
Institut des Maladies Métaboliques et Cardiovasculaires

PAYS DE LA LOIRE
ANGERS
Structure-function relationship of the TSH receptor and of the related receptors
CHU d'Angers
Plateau de Biologie et Médecine Moléculaire

EMILIA ROMAGNA
MODENA
Pseudoxanthoma elasticum: from the understanding of pathogenetic mechanisms towards therapeutic perspectives
Università degli Studi di Modena e Reggio Emilia
LabGen - Laboratorio Sequenziamento Genomico

LIGURIA
GENOVA
Functional and structural studies of human CLC chloride proteins involved in genetic diseases
Consiglio Nazionale delle Ricerche
Istituto di Biofisica

LOMBARDIA
ROZZANO
Functional dissection of the molecular underpinnings of 7q11.23 syndromes: bridging pathogenic insight to drug discovery at single cell resolution
IRCCS Istituto Clinico Humanitas
Istituto Clinico Humanitas

Ontario
TORONTO
iPS cells to model vascular disease in patients with Williams Beuren syndrome
Hospital for Sick Children, Research Institute

Gelderland
NIJMEGEN
HNF1ß: master regulator of cilia formation and electrolyte homeostasis in ADTKD-HNF1ß patients
Radboudumc - Radboud universitair medisch centrum
Afdeling Fysiologie

NORTE
PORTO
Alport Syndrome: Clinical and molecular study of Portuguese families
Faculdade de Medicina da Universidade do Porto
Unidade de Investigação e Desenvolvimento de Nefrologia

NORTE
PORTO
LIMP-2 studies: from clinical genetics to functional genomics and back (studies in action myoclonus-renal failure syndrome (AMRF))
Instituto de Biologia Molecular e Celular
Unidade de Biologia do Lisossoma e do Peroxissoma

SUL
LISBOA
Functional and genetic analysis of WNK protein kinases involved in Gordon syndorme
Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
Unidade de Investigação e Desenvolvimento

Suisse Alémanique
ZÜRICH
Role of PKD1 and WNK4 in the regulation of the renal thiazide-sensitive NaCl cotransporter NCC
Universität Zürich
Anatomisches Institut

Suisse Alémanique
ZÜRICH
Genetic and molecular contributors to adrenocortical hormone excess
Universitätsspital Zürich
Klinik für Endokrinologie, Diabetologie und Klinische Ernährung

Suisse Romande
FRIBOURG
The Differential Roles of Positive Emotions and Emotion Regulation for Socio-Emotional Processes in Developmental Disabilities: Insights for Future Interventions
Universität Freiburg
Heilpädagogisches Institut

Suisse Romande
GENÈVE
Non-cell-autonomous circadian regulation of brain function
UNIGE Université de Genève
Département de Génétique et Evolution

Asturias
OVIEDO
Application of RenalTube to patients needs and clinical and experimental research on distal renal tubular acidosis and hypophosphatemic rickets linked to the X chromosome
Fundación para la Investigación Biosanitaria del Principado de Asturias
FINBA: Fundación para la Investigación Biosanitaria del Principado de Asturias

Cataluña
BADALONA
Impact of cellular, genetic and epigenetic heterogeneity in the progression and treatment of peripheral nervous system tumors associated to Neurofibromatosis type 1
Instituto de Investigación Germans Trias i Pujol
Fundació Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol

Cataluña
BARCELONA
Role of Apolipoprotein A-Ib in the idiopathic nephrotic syndrome
Vall d'Hebron Institut de Recerca VHIR
Grupo de investigación en nefrología y trasplante renal

Madrid
MADRID
Quantitative profiles of complement FH/FHR proteins as biomarkers of disease predisposition and evolution in primary and secondary haemolytic uraemic syndrome
IdiPAZ - Instituto de Investigación Sanitaria del Hospital Universitario La Paz
Laboratorio de Inmunopatología del Complemento

Connecticut
CHESHIRE
CCRN 1093 (aHUS): An observational, non-interventional multicenter, multinational study of patients with Atypical HemolyticUremic Syndrome (aHUS Registry)
Alexion Pharmaceuticals, Inc.

Washington
ADDRESS: NOT PROVIDED - US
Targeting tumors with nf1 loss
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Clinical and genetic studies of vacterl association
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Genomic analysis in genes responsible for eye abnormalities in patients
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Molecular and signaling mechanisms of peripheral nerve sheath tumorigenesis
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Mechanisms of nf1 pathophysiology underlying hyperactivity
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Social competence in youth with neurofibromatosis type 1
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Project 1: gene networks for social cognition in williams syndrome
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Project 2: modeling williams syndrome using human neurons
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Project 3: cellular architectonics and local circuits
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Project 4: neuroimaging of social circuitry
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Project 5: characterization of social phenotype
Institution: Information not provided - US

Tyne & Wear
NEWCASTLE UPON TYNE
The Role of Membrane Attack Complex in Atypical Haemolytic Uraemic Syndrome
Institute of Cellular Medicine, Newcastle University, Medical School
Institute of Cellular Medicine

OOST-VLAANDEREN
GENT
ImmunAID: Immunome Project Consortium for Autoinflammatory Disorders - BE
VIB headquarters
VIB (vlaams instituut voor biotechnologie) headquarters

VLAAMS BRABANT
LEUVEN
ImmunAID: Immunome Project Consortium for Autoinflammatory Disorders - BE
UZ Leuven - Campus Gasthuisberg
Pediatric Rheumatology

Baden-Württemberg
HEIDELBERG
ReDox : Repurposing von Doxycyclin zur Behandlung von Patienten mit AL-Amyloidose -DE-
Zentrum für Innere Medizin (Krehl-Klinik)
Abteilung Innere Medizin V - Hämatologie, Onkologie und Rheumatologie

Baden-Württemberg
TÜBINGEN
ESPED-Studie: Omphalozelen und assoziierte Fehlbildungen bei Neu- und Frühgeborenen
Universitätsklinik für Kinder- und Jugendmedizin Tübingen
Abteilung für Neonatologie

Bayern
ERLANGEN
STOP-FSGS: Lösliche Faktoren bei FSGS
Internistisches Zentrum des Universitätsklinikums Erlangen
Medizinische Klinik 4 - Nephrologie und Hypertensiologie

Berlin
BERLIN
Der Einfluss der extrakorporalen Photopherese auf die Sklerose der Haut - eine klinische Sondierungsstudie
Charité - Universitätsmedizin Berlin (CCM)
Clinical Research Center for Hair and Skin Science

Berlin
BERLIN
ActiMON: Aktivitätsmonitoring bei Jugendlichen und jungen Erwachsenen mit rheumatischen und muskuloskelettalen Erkrankungen
Deutsches Rheuma-Forschungszentrum Berlin
Forschungsbereich Epidemiologie

Hamburg
HAMBURG
Prospektive Anfangs-Kohortenstudie bei juveniler systemischer Sklerose
Schön Klinik Hamburg Eilbek
Hamburger Zentrum für Kinder- und Jugendrheumatologie

Hessen
FRANKFURT AM MAIN
TIF1-gamma Projekt: Immunhistochemische Analyse von "transkription intermediaty faktor-1gamma" (TIF1-gamma) Antikörper in der Haut von erwachsenen Patienten mit anti-TIF1-gamma-positiver Dermatomyositis
Universitätsklinikum Frankfurt
Klinik für Dermatologie, Venerologie und Allergologie

Niedersachsen
HANNOVER
TIF1-gamma Projekt: Immunhistochemische Analyse von "transkription intermediaty faktor-1gamma" (TIF1-gamma) Antikörper in der Haut von erwachsenen Patienten mit anti-TIF1-gamma-positiver Dermatomyositis
Medizinische Hochschule Hannover
Klinik für Dermatologie, Allergologie und Venerologie

Nordrhein-Westfalen
KÖLN
Genomische Analysen und Entwicklung epigenetischer Biomarker bei Steroid-resistentem nephrotischem Syndrom (KFO 329)
Institut für Humangenetik am Universitätsklinikum Köln
Institut für Humangenetik

Nordrhein-Westfalen
KÖLN
Die Bedeutung einer gestörten Schlitzmembran-Signaltransduktion bei der Entstehung der FSGS (KFO 329)
Universitätsklinikum Köln
Klinik II für Innere Medizin - Nephrologie, Rheumatologie, Diabetologie und allgemeine Innere Medizin

Nordrhein-Westfalen
KÖLN
TIF1-gamma Projekt: Immunhistochemische Analyse von "transkription intermediaty faktor-1gamma" (TIF1-gamma) Antikörper in der Haut von erwachsenen Patienten mit anti-TIF1-gamma-positiver Dermatomyositis
Universitätsklinikum Köln
Klinik und Poliklinik für Dermatologie und Venerologie

Rheinland-Pfalz
LUDWIGSHAFEN
Vaskulitis-Register RLP/S: Prospektive Untersuchung der Diagnostik und Therapie von Vaskulitiden in Rheinland-Pfalz/Saarland
Klinikum der Stadt Ludwigshafen gGmbH
Klinik für Innere Medizin, Hämato-Onkologie, Nephrologie, Infektiologie und Rheumatologie

Sachsen-Anhalt
DESSAU
Epidemiologie der Behçet-Krankheit in Deutschland
Städtisches Klinikum Dessau
Klinik für Dermatologie, Venerologie und Allergologie / Immunologisches Zentrum

Sachsen-Anhalt
DESSAU
Prognostische Kriterien der Behçet-Krankheit
Städtisches Klinikum Dessau
Klinik für Dermatologie, Venerologie und Allergologie / Immunologisches Zentrum

Schleswig-Holstein
LÜBECK
Generierung und Charakterisierung eines Antikörper-basierten Mausmodells für die systemische Sklerose
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Klinik für Rheumatologie und Klinische Immunologie

AUVERGNE-RHONE-ALPES
BRON
Genetic transmission of familial forms of sarcoidosis
CHU de Lyon HCL - GH Est
Unité Médicale de Génétique des Cancers et des Maladies Multifactorielles

AUVERGNE-RHONE-ALPES
BRON
Genetic transmission of familial forms of sarcoidosis
CHU de Lyon HCL - GH Est-Hôpital Louis Pradel
Service de pneumologie

ILE-DE-FRANCE
PARIS
Evaluation and treatement of scleroderma
AP-HP.Sorbonne Université - Hôpital Saint-Antoine
Service de médecine interne

ILE-DE-FRANCE
PARIS
PLA2R-negative extramembranous glomerulopathies: antigens, models and patients
Groupe hospitalier AP-HP.6 - Hôpital Tenon
INSERM UMRS 1155 "Des maladies rénales aux maladies fréquentes, remodelage et réparation"

OCCITANIE
TOULOUSE
Validation of a Fetal Urine Peptidome-based Classifier to Predict Post-natal Renal Function in Posterior Urethral Valves (Antenatal)
CHU de Toulouse - Hôpital des Enfants
Pédiatrie - Néphrologie, médecine interne et hypertension

PROVENCE-ALPES-COTE D'AZUR
VALBONNE
Dynamics of anti-PLA2R1 and anti-THSD7A autoantibodies in patients with extramembranous glomerulonephritis: from early stages to active disease
IPMC - Institut de Pharmacologie Moléculaire et Cellulaire
Equipe "Physiopathologie moléculaire des phospholipases A2 & de leurs médiateurs"

CAMPANIA
NAPOLI
DESSCIPHER: Development and Prevention of Severe Heart Disease in Systemic Sclerosis (terminated)
AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani
Divisione di Reumatologia

CAMPANIA
NAPOLI
DESSCIPHER: Development and prevention of pulmonary hypertension in systemic sclerosis (terminated)
AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani
Divisione di Reumatologia

CAMPANIA
NAPOLI
Prevention and Treatment of Digital Ulcers in Systemic Sclerosis - IT (terminated)
AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani
Divisione di Reumatologia

LOMBARDIA
BERGAMO
Unravelling the role of PAX2 mutations in human Focal Segmental Glomerulosclerosis
IRCCS Mario Negri - Centro Anna Maria Astori
Dipartimento Medicina Molecolare

LOMBARDIA
RANICA
Identification of new genes associated to familial idiopathic steroid-resistant nephrotic syndrome
Istituto di Ricerche Farmacologiche Mario Negri
Centro di Ricerche Cliniche per le Malattie Rare

TOSCANA
FIRENZE
DESSCIPHER: Development and Prevention of Severe Heart Disease in Systemic Sclerosis (terminated)
AOU Careggi
S.O.D. di Reumatologia

TOSCANA
FIRENZE
DESSCIPHER: Development and prevention of pulmonary hypertension in systemic sclerosis (terminated)
AOU Careggi
S.O.D. di Reumatologia

TOSCANA
FIRENZE
Prevention and Treatment of Digital Ulcers in Systemic Sclerosis - IT (terminated)
AOU Careggi
S.O.D. di Reumatologia

JAPAN
NAGASAKI
Investigation of Adult Still's disease in precision medicine to create evidences that facilitate the revision of diagnostic criteria through nation-wide clinical research network
Nagasaki University Graduate School of Biomedical Sciences
Department of Immunology and Rheumatology

Ontario
TORONTO
The Effect of Creatine Supplementation on Muscle Function in Childhood Myositis
Hospital for Sick Children, Research Institute

Utrecht
NIEUWEGEIN
Genetic predisposition to interstitital lung diseases and disease phenotypes
St. Antonius Ziekenhuis, locatie Nieuwegein
Longcentrum

Østlandet
OSLO
Prediction of response to immunosuppressive treatment in Systemic sclerosis (Precise)
Oslo University Hospital
Avdeling for revmatologi, hud- og infeksjonssykdommer

Østlandet
OSLO
'The Norwegian, nationwide Systemic Sclerosis cohort; a novel tool for cardiopulmonary, gastro-intestinal and cancer risk evaluation; (NORSE Care study) from beside to bench'
Oslo University Hospital
Avdeling for revmatologi, hud- og infeksjonssykdommer

WIEN
WIEN
Systems medicine analysis of sarcoidosis by targeting mTOR in a co-clinical trial in patients and mice
Allgemeines Krankenhaus der Stadt Wien
Universitätsklinik für Dermatologie

Region Skåne
LUND
Mycophenolate Mofetil Pharmacokinetics in Systemic Sclerosis (MMFSSC)
Skåne University Hospital, Lund

Region Stockholm
STOCKHOLM
Molecular and clinical studies of bladder exstrophy and congenital adrenal hyperplasia
Karolinska Institutet - Solna
Department of Women's and Children's Health

Andalucía
SEVILLA
Autophagy and inflammation: model in classic autoinflammatory syndromes and Behçet's disease
IBIS - Instituto de Biomedicina de Sevilla
Grupo de Inmunología

Cataluña
BADALONA
Use of artificial intelligence and systems biology for diagnosis and personalized risk assessment for inherited kidney diseases, focusing on Alport syndrome
Instituto de Investigación Germans Trias i Pujol
Grupo de investigación en Mecanismos epigenéticos del cáncer y diferenciación celular

Cataluña
BARCELONA
Use of artificial intelligence and systems biology for diagnosis and personalized risk assessment for inherited kidney diseases, focusing on Alport syndrome
Universitat Politècnica de Catalunya
Departamento de Ingeniería de Sistemas, Automática e Informática Industrial

Madrid
ALCORCÓN
Deciphering the role of factor-H related proteins in complement-related kidney diseases
Hospital Universitario Fundación Alcorcón
Servicio de Nefrología

Madrid
MADRID
Use of artificial intelligence and systems biology for diagnosis and personalized risk assessment for inherited kidney diseases, focusing on Alport syndrome
Hospital Universitario Fundación Jiménez Díaz
Servicio de Nefrología e Hipertensión

Madrid
MADRID
Deciphering the role of factor-H related proteins in complement-related kidney diseases
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en Nefrología Clínica

Washington
ADDRESS: NOT PROVIDED - US
Juvenile myositis
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Genetic analysis of complex inflammatory disorders
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Genetics; natural history; and pathophysiology of behcet's disease
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Genetics; pathophysiology; and treatment of recessive autoinflammatory diseases
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Genetic; cellular and molecular mechanisms in autoimmunity to retina
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Immunogenetic mechanisms in behcet's disease
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Contribution of adipocytes and adipose secreted factors to fibrosis in systemic sclerosis
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Systemic sclerosis (ssc) vasculopathy: improved clinical monitoring and treatment
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Systemic sclerosis-associated interstitial lung disease response index
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Animal care: supporting research on pathogenesis and treatment of autoimmunity
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Connective tissue diseases/inflammatory myopathies--polymyositis/dermatomyositis
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Immunopathogen autoimmune inflammatory myopathies--polymyositis/dermatomyositis
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Pathogenesis of behcet's disease and still's disease
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Project 1 biomarkers of disease activity and progression in systemic sclerosis
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Project 1: systemic sclerosis skin biomarkers & therapeutics
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Project 3: targeting pro-fibrotic e3 ligases in systemic sclerosis
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Translational immunology research: a support for clinical immunological research
Institution: Information not provided - US

Cambridgeshire
CAMBRIDGE
Pathogenic mechanisms and effects of treatment in chronic, idiopathic inflammatory myopathies, myositis
University of Cambridge
Department of Medicine

Greater London
LONDON
Sub-phenotyping in juvenile dermatomyositis (JDM), a rare and serious autoimmune childhood disorder, within the UK JDM Cohort and Biomarker Study: from phenotype to stratified treatments
GOSH NHS Foundatin Trust
Juvenile Dermatomyositis Research Centre

North Yorkshire
COTTINGHAM
Exploring the Immunology of Sarcoidosis
Castle Hill Hospital

Bayern
MÜNCHEN
Etablierung von Oberflächenplasmonenresonanz (SPR) Tests zur verbesserten Diagnostik von Autoimmunerkrankungen
Klinikum rechts der Isar der Technischen Universität München
Arbeitsgruppe Biosensorik

Rheinland-Pfalz
MAINZ
Die Wirkung von körperlicher Aktivität und Belimumab auf die chronische Erschöpfung (Fatigue) und die Anti-NR2-Antikörper bei SLE Patienten
Universitätsmedizin Mainz
I. Medizinische Klinik und Poliklinik

ILE-DE-FRANCE
PARIS
Model contribution in the microeconomic assessment of therapeutic strategies in Wegener granulomatosis
AP-HP.Centre - Université de Paris - Hôpital Cochin
Service de Santé publique : Gestion des risques et qualité

LAZIO
ROMA
Identification of biological and imaging events that predict the progression of Takayasu arteritis (TA) vascular lesions
ISS - Istituto Superiore di Sanità
Centro di Riferimento per la Medicina di Genere

PUGLIA
BARI
Physiopathology of HCV-related Cryoglobulinemic Vasculitis: molecular, immunological and clinical analisys
Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Unità di Epatologia - Sezione di Medicina Interna e Oncologia Clinica

Ontario
TORONTO
Genetics of Rare Systemic Inflammatory Diseases
The Hospital for Sick Children
Genetics and Genome Biology

WIEN
ADDRESS: NOT PROVIDED - AT
SABLE: A 5-Year Prospective Observational Registry to Assess Adverse Events of Interest and Effectiveness in Adults With Active, Autoantibody-Positive Systemic Lupus Erythematosus Treated With or Without BENLYSTA (Belimumab) - AT
Institution: Information not provided - AT

Suisse Alémanique
BASEL
Longitudinal Imaging in Patients With Large Vessel Vasculitis to Predict Further Disease Course
Universitätsspital Basel
Rheumatologie

Andalucía
ARMILLA
Identification of functionally relevant genetic variants associated with GCA - ES
Instituto de Parasitología y Biomedicina "López-Neyra"
Bases genéticas de las enfermedades autoinmunes

Cataluña
BARCELONA
Systems biology and bioinformatics approaches to provide a holistic understanding of GCA biology - ES
Anaxomics Biotech SL - Barcelona

Cataluña
BARCELONA
BeliLES: Effectiveness, Tolerability, and Safety of Belimumab in Patients With Systemic Lupus Erythematosus Treated at the Spanish Departments of Internal Medicine
Hospital Clínic de Barcelona
Servicio de Enfermedades Autoinmunes

Cataluña
BARCELONA
Multimodal imaging study for the diagnosis and prognosis of patients with systemic lupus erythematosus
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)
Institut d'Investigacions Biomèdiques August Pi i Sunyer

Cataluña
BARCELONA
Functional characterisation of inflammation and vascular remodelling pathways in GCA - ES
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)
Grupo de investigación en enfermedades autoinmunes sistémicas

Madrid
MADRID
Study of the relevance of PSGL-1/P-selectin interaction in the cellular proteostasis and implication in the pathogenesis of scleroderma and lupus
IIS Princesa - Instituto de Investigación del Hospital de La Princesa
Fundación Biomédica del Hospital de La Princesa

Washington
ADDRESS: NOT PROVIDED - US
Direct regulation of extracellular proteostasis by the unfolded protein response
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Addressing critical knowledge gaps in early diffuse scleroderma trial design
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Characterizing the takayasu arteritis genetic risk in rps9/lilrb3
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Nasal microbiome and host immunity in granulomatosis with polyangiitis
Institution: Information not provided - US

Washington
ADDRESS: NOT PROVIDED - US
Biomarkers of pulmonary complications of scleroderma: the ssc-pah and
Institution: Information not provided - US

West Yorkshire
LEEDS
GCA Consortium - Clinical and immunogenetic characterization of Giant Cell Arteritis (GCA) and polymyalgia rheumatica (PMR)
Leeds Institute of Rheumatic and Musculoskeletal Medicine
Molecular Rheumatology Group

West Yorkshire
LEEDS
Clinical and Immunogenetic Characterization of Giant Cell Arteritis (GCA) and Polymyalgia Rheumatica (PMR)
University of Leeds
Leeds institute of clinical trials

West Yorkshire
LEEDS
MICA: Treatment According to Response in Giant cEll arTeritis (TARGET)
University of Leeds
The University of Leeds

West Yorkshire
LEEDS
Linking public and GCA datasets to identify novel pathogenic pathways -GB
University of Leeds
The University of Leeds
Multizentrische Forschungsprojekte
- Cliniques universitaires Saint-Luc - UCLouvain
- Laboratory of Nephrology
- Zentrum für Kinder- und Jugendmedizin des Universitätsklinikums Heidelberg
- Klinik für Kinderheilkunde I - Sektion Pädiatrische Nephrologie
- Trinity College Dublin
- ADAPT Centre
- IMAGINE - Institut des Maladies Génétiques
- Equipe "Base moléculaire des maladies rénales héréditaires: néphronophtise et hypodysplasie"
- Radboudumc - Radboud universitair medisch centrum
- Afdeling Fysiologie
- Institution: Information not provided - PL
- Centre de Recherches des Cordeliers (CRC)
- Equipe "Métabolisme et Physiologie Rénale"
- Fondation René Touraine
- Institut de Recherche sur la Peau, Fondation René Touraine
- Adienne S.R.L.
- IRCCS Istituto Europeo di Oncologia
- Stem cell epigenetics Unit
- Fondazione IRCCS Policlinico San Matteo
- Clinica Medica III
- The Mount Sinai School of Medicine
- Department of pediatric endocrinology
- Department of Health
- Birmingham Children's Hospital NHS Foundation Trust
- Department of Nephrology
- Zentrum für Kinder- und Jugendmedizin des Universitätsklinikums Heidelberg
- Klinik für Kinderheilkunde I - Sektion Pädiatrische Nephrologie
- Kerckhoff-Klinik GmbH
- Abteilung für Rheumatologie und klinische Immunologie
- Universitätsklinikum Aachen
- Institut für Humangenetik
- Universitätsklinikum Aachen
- Klinik für Nieren- und Hochdruckkrankheiten, rheumatologische und immunologische Erkrankungen (Med. Klinik II)
- Universitätsklinikum Aachen
- Klinik für Nieren- und Hochdruckkrankheiten, rheumatologische und immunologische Erkrankungen (Med. Klinik II)
- Universitätsklinikum Magdeburg A.ö.R
- MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
- GHU AP-HP Nord. Université de Paris - Hôpital Saint-Louis
- MATHEC - Maladies Auto-Immunes et Thérapie Cellulaire
- Institut National de la Santé et de la Recherche Médicale
- Ospedale San Giuseppe Multimedica
- Il Polmone.it - Malattie Rare Polmonari
- Fondazione IRCCS Policlinico San Matteo
- Dipartimento di Medicina Molecolare
- GOSH NHS Foundatin Trust
- Rheumatology Unit
- Alder Hey Children's Hospital
- Department of Rheumatology

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS
EUNEFRON: the European network for the study of orphan nephropathies

Baden-Württemberg
HEIDELBERG
EURENOMICS: European Consortium for High-Throughput Research in Rare Kidney Diseases (TERMINATED)

County Dublin
DUBLIN
HELICAL - Health Data Linkage for Clinical Benefit

ILE-DE-FRANCE
PARIS
AnBiCyst : Functional characterization of ANKS6/ANKS3/BICC1 complex and implication in cystic kidney diseases

Gelderland
NIJMEGEN
FIGHT-CNNM2: For Improving diagnostics and Grasping the disease mechanisms of rare Hypomagnesemia in paTients with CNNM2 mutations

Kraków
ADDRESS: NOT PROVIDED - PL
EPISTOP: Long-term, prospective study evaluating clinical and molecular biomarkers of epileptogenesis in a genetic model of epilepsy - tuberous sclerosis complex

ILE-DE-FRANCE
PARIS
Réseau européen de recherche sur les acidoses tubulaires rénales

ILE-DE-FRANCE
PAROS
TAG: TogetherAgainstGenodermatoses - improving health care and social support for patients and family affected by severe genodermatoses

LOMBARDIA
CAPONAGO
PRATH: preclinical study of recombinant human anti-C5 for the treatment of atypical hemolytic uremic syndrome (TERMINATED)

LOMBARDIA
MILANO
DISEASEAVATARS: Modeling Disease through Cell Reprogramming: a Translational Approach to the Pathogenesis of Syndromes Caused by Symmetrical Gene Dosage Imbalances

LOMBARDIA
PAVIA
EUPLANE: EUropean PLAtelet NEtwork for studying physiopathology of two inherited thrombocytopenias, THC2 and MYH9-RD, characterized by genetic alterations of RUNX1-target genes

New York
NEW YORK
RGSDC: Rare Genetic Steroid Disorders Consortium

Greater London
LONDON
RASopathy network: disorders of the Ras-MAPK pathway

West Midlands
BIRMINGHAM
European Paediatric Research for Hemolytic Uremic Syndrome (HUS)

Baden-Württemberg
HEIDELBERG
PODONET: consortium for clinical, genetic and experimental research into hereditary diseases of the podocyte

Hessen
BAD NAUHEIM
DESSCIPHER: Europäisches Forschungsprojekt zur Therapieoptimierung der Systemischen Sklerose

Nordrhein-Westfalen
AACHEN
EUCID.net: Europäisches Netzwerk für angeborene Imprinting-Erkrankungen

Nordrhein-Westfalen
AACHEN
Rare-G: The Epidermal Growth Factor System in Rare Glomerular Disease: From Molecular Mechanisms to Therapeutics

Nordrhein-Westfalen
AACHEN
STOP-FSGS: Speed Translation-Oriented Progress to diagnose and treat focal segmental glomerulosclerosis (FSGS)

Sachsen-Anhalt
MAGDEBURG
International Clearinghouse for Birth Defects Monitoring Systems

ILE-DE-FRANCE
PARIS
NISSC-2 : Post AHSCT (Autologous Hematopoietic Stem Cell Transplantation) management for patients with systemic sclerosis: a prospective, non-interventional approach across Europe

ILE-DE-FRANCE
PARIS
ImmunAID: Immunome Project Consortium for Autoinflammatory Disorders

LOMBARDIA
MILANO
Il Polmone.it - Malattie Rare Polmonari

LOMBARDIA
PAVIA
ReDox : Repurposing doxycycline in the treatment of AL amyloidosis

Greater London
LONDON
ENJD: European Network for Juvenile Dermatomyositis

Merseyside
LIVERPOOL