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Research projects
GERMANY
Berlin
BERLIN
EURDYSCOVER: Pathophysiology of dystonia - role of gene-environment interaction and common pathophysiological pathways -DE
Charité - Universitätsmedizin Berlin
Sektion Bewegungsstörungen und Neuromodulation, Campus Mitte und Campus Virchow Klinikum
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
Qhts to identify inhibitors of dyt1 inclusion formation
Institution: Information not provided - US
FRANCE
ILE-DE-FRANCE
PARIS
EURDYSCOVER: Pathophysiology of dystonia - role of gene-environment interaction and common pathophysiological pathways - FR
AP-HP.Sorbonne Université - Hôpital de la Pitié-Salpêtrière
Unité fonctionnelle Maladie de Parkinson et Pathologies du Mouvement
ITALY
LAZIO
ROMA
EURDYSCOVER: Fisiopatologia della distonia - ruolo dell'interazione geni-ambiente e processi fisiopatologici comuni - IT
IRCCS Fondazione Santa Lucia - CERC
Laboratorio di Neurofisiologia e Plasticità
UNITED STATES
Arizona
PHOENIX
The etiology of inherited neurological diseases
Phoenix Children's Hospital
Barrow Neurological Institute
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
Patholog-omics - essential tremor in the broader context of neurodegeneration
Institution: Information not provided - US
FINLAND
Finland
OULU
Novel Diagnostics and Treatment Strategies for Developmental Disorders, Childhood Epilepsies and Movement Disorders
University of Oulu
Biocenter Oulu
FRANCE
ILE-DE-FRANCE
PARIS
Neuroglobin gene overexpression: a promising tool for treating a large spectrum of neurological disorders thanks to its ability to safely and sustainably preserve mitochondrial integrity
Institut National de la Santé et de la Recherche Médicale
ITALY
LAZIO
ROMA
Diverse rare diseases caused by functional dysregulation of Rho GTPase-related proteins
ISS - Istituto Superiore di Sanità
Centro Nazionale Malattie Rare
SPAIN
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
SPAIN
Madrid
MADRID
RAREGenomics: Network of Genomic, Functional, Clinical and Therapeutic Resources for the Study of Rare Neurological Diseases
Hospital Universitario Fundación Jiménez Díaz
Servicio de Genética Clínica
CANADA
Colombie-Britannique
VICTORIA
Silent Genomes: Reducing health care disparities and improving diagnostic success for children with genetic diseases from Indigenous populations
University of Victoria
Community Genetics Research Program/Island Medical Program
CANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
SPAIN
Madrid
MADRID
Identification 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
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
A powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US
Multicentric Research projects
- Neurologische Klinik und Poliklinik des Universitätsklinikums Würzburg
- Neurologische Klinik und Poliklinik
- Fondazione IRCCS Istituto Neurologico "Carlo Besta"
- Neurologia I
- Azienda Ospedaliera di Padova
- Clinica Pediatrica
- Haukeland University Hospital
GERMANY
Bayern
WÜRZBURG
EURDYSCOVER: Pathophysiology of dystonia - role of gene-environment interaction and common pathophysiological pathways
ITALY
LOMBARDIA
MILANO
European network for the study of dystonia syndromes
ITALY
VENETO
PADOVA
Brains for brain: research group of the European task force on brain and neurodegenerative lysosomal storage diseases
NORWAY
Vestlandet
BERGEN