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Research projects
GERMANY
Bayern
WÜRZBURG
DYSTRACT: Generation of novel DYT1, DYT6 and DYT12 mouse and rat models of dystonia
Institut für Klinische Neurobiologie der Universität Würzburg
Institut für Klinische Neurobiologie
GERMANY
Bayern
WÜRZBURG
DYSTRACT: System physiology of dystonia development in rodent models of DYT1 and DYT12
Neurologische Klinik und Poliklinik des Universitätsklinikums Würzburg
Neurologische Klinik und Poliklinik
GERMANY
Mecklenburg-Vorpommern
ROSTOCK
Genetical and biochemical characterisation of DYT1 dystonia
Klinik für Neurologie und Poliklinik der Universitätsmedizin Rostock
Klinik für Neurologie und Poliklinik
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
Qhts to identify inhibitors of dyt1 inclusion formation
Institution: Information not provided - US
FRANCE
OCCITANIE
MONTPELLIER
Comparative Efficacy of Genome vs Exome Sequencing Approaches for the Diagnosis of Dystonias
IURC - Institut Universitaire de Recherche Clinique
Laboratoire de génétique moléculaire
GERMANY
Baden-Württemberg
TÜBINGEN
Genetic Basis of Dystonia in Turkish families
Hertie-Institut für klinische Hirnforschung (HIH)
Abteilung Neurologie mit Schwerpunkt neurodegenerative Erkrankungen
GERMANY
Baden-Württemberg
TÜBINGEN
Genetic Basis of Dystonia in Turkish families
Institut für Medizinische Genetik und angewandte Genomik Tübingen
Institut für Medizinische Genetik und angewandte Genomik
GERMANY
Bayern
WÜRZBURG
DYSTRACT: Network on research and management of rare dystonia (coordination)
Neurologische Klinik und Poliklinik des Universitätsklinikums Würzburg
Neurologische Klinik und Poliklinik
GERMANY
Berlin
BERLIN
DYSTRACT: Genetic fingerprints of oscillatory network activity in dystonia
Charité - Universitätsmedizin Berlin
Sektion Bewegungsstörungen und Neuromodulation, Campus Mitte und Campus Virchow Klinikum
GERMANY
Hessen
MARBURG
DYSTRACT: IT platform for the Dystonia Translational Research and Therapy Consortium
Universitätsklinikum Gießen und Marburg GmbH, Standort Marburg
Kompetenznetz Parkinson - Netzwerk Sekretariat
GERMANY
Schleswig-Holstein
LÜBECK
Phenotypic spectrum and molecular characterization of Movement disorders
Universität Lübeck
Institut für Neurogenetik
GERMANY
Schleswig-Holstein
LÜBECK
DYSTRACT: Elucidation of novel genetic causes and modifiers for dystonia
Universität Lübeck
Institut für Neurogenetik
GERMANY
Schleswig-Holstein
LÜBECK
DYSTRACT: Modeling dystonia in an endogenous human cellular system: Platform and characterization of iPS derived neurons from patients with monogenic isolated dystonia
Universität Lübeck
Institut für Neurogenetik
GERMANY
Schleswig-Holstein
LÜBECK
DYSTRACT: Defining motor system endophenotypes in dystonia using a multimodal neurophysiology and structural imaging approach
Universität Lübeck
Institut für Neurogenetik
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
FRANCE
ILE-DE-FRANCE
PARIS
STaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
FRANCE
PAYS DE LA LOIRE
NANTES
FROGH : FRench Regional Origins in Genetics for Health - FR
Institut de Recherche en Santé - Université de Nantes
L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
ITALY
CAMPANIA
NAPOLI
Telethon Undiagnosed Disease Program - Revised Proposal
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine
JAPAN
JAPAN
AICHI
Management ofthe clinical diagnostic centre for rare intractable diseases with genome instability and development of potential therapeutic medicine
Research Institute of Environmental Medicine, Nagoya University
JAPAN
JAPAN
AICHI
Establishment of the Next-generation Muti-omics Clinical Diagnostic Centre for rare intractable diseases with genome instability
Research Institute of Environmental Medicine, Nagoya University
JAPAN
JAPAN
TOKYO
Formation of integrated omics analysis base of refractory diseases in children and perinatal period
National Center for Child Health and Development
Research Institute
Multicentric Research projects
- CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
- Unité fonctionnelle Maladie de Parkinson et Pathologies du Mouvement
- Universitätsklinikum Aachen
- GeNeMove - Netzwerksekretariat
- Neurologische Klinik und Poliklinik des Universitätsklinikums Würzburg
- Neurologische Klinik und Poliklinik
- Fondazione IRCCS Istituto Neurologico "Carlo Besta"
- Neurologia I
- Zentrum für Neuropathologie und Prionforschung (ZNP)
- Zentrum für Neuropathologie und Prionforschung der LMU München
- Hospital Universitari de Bellvitge
- Unidad de Neuropatología
- University of British Columbia
- Maternal Infant Child and Youth Research Network
- Muséum National d'Histoire Naturelle
- Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
- Institut de Recherche en Santé - Université de Nantes
- L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
- IRCCS Ospedale Pediatrico Bambino Gesù - SEDE GIANICOLO
- Servizio Clinico di Consulenza Genetica
FRANCE
ILE-DE-FRANCE
PARIS
Réseau national des dystonies
GERMANY
Nordrhein-Westfalen
AACHEN
GeNeMove: German Network of Hereditary Movement Disorders
GERMANY
Bayern
WÜRZBURG
DYSTRACT: Network on research and management of rare dystonia
ITALY
LOMBARDIA
MILANO
European network for the study of dystonia syndromes
GERMANY
Bayern
MÜNCHEN
BNE: BrainNet Europe II: European brain tissue bank
SPAIN
Cataluña
L'HOSPITALET DE LLOBREGAT
CIEN: Spanish Network for Cooperative Research in Neurological diseases
CANADA
Colombie-Britannique
VANCOUVER
Maternal Infant Child and Youth Research Network (MICYRN)
FRANCE
ILE-DE-FRANCE
PARIS
STaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy
FRANCE
PAYS DE LA LOIRE
NANTES
FROGH : FRench Regional Origins in Genetics for Health
ITALY
LAZIO
ROMA