Partnership : Academics = 
, Industrials = 
, Financial investitors = 
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- CANADA
- Colombie-Britannique
- VANCOUVER
- FORGE - Finding of Rare Disease Genes in Canada
- University of British Columbia
- Faculty of Medicine
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- CANADA
- Ontario
- OTTAWA, ONTARIO
- FORGE - Finding of Rare Disease Genes in Canada
- University of Ottawa
- Faculty of Medicine -
- More details
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- FORGE - Finding of Rare Disease Genes in Canada
- Centre hospitalier universitaire Sainte-Justine
- Pédiatrie
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- Study of the molecular pathogenesis and development of therapeutic approaches for myotonic dystrophy
- The Cyprus Institute of Neurology and Genetics
- Department of molecular genetics A
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- FRANCE
- AUVERGNE
- CLERMONT-FERRAND
- MYORES: Multi-organismic approach to study normal and aberrant muscle development, function and repair
- Faculté de médecine de Clermont-Ferrand
- Laboratoire de Génétique, Reproduction et Développement
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- FRANCE
- ILE-DE-FRANCE
- EVRY
- NMD-CHIP: design, production and technical validation of candidate genes targeted chips (WP3)
- Généthon
- Généthon - Banque d'ADN et de cellules
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- FRANCE
- ILE-DE-FRANCE
- GARCHES
- Tolerability and efficiency of the precoce use of non invasive nocturnal mechanical ventilation in adult affected by myotonic dystrophy
- GHU Paris Île-de-France Ouest - Hôpital Raymond Poincaré
- Service de réanimation et unité de ventilation à domicile
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- FRANCE
- NORD-PAS-DE-CALAIS
- LILLE
- NEUROSPLICEDETAU: involvement and lack of correction of splicing of Tau in myotonic dystrophy
- Faculté de médecine de Lille
- Maladies neurodégénératives et mort neuronale
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- FRANCE
- PROVENCE-ALPES-COTE D'AZUR
- MARSEILLE
- NMD-CHIP: chip design, synthesis and technical validation for known genes involved in neuromuscular diseases (WP2)
- CHU de Marseille - Hôpital de la Timone
- Laboratoire de génétique moléculaire
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- FRANCE
- PROVENCE-ALPES-COTE D'AZUR
- NICE
- Study of proliferation and differentiation of myoblasts in muscular dystrophies
- Faculté de médecine de Nice Sophia-Antipolis
- Cellules souches et différenciation
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- BNE: BrainNet Europe II: European brain tissue bank - Network for clinical neuroscience and basic research (coordination)
- Ludwig-Maximilians-Universität München
- Zentrum für Neuropathologie und Prionforschung
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- Identification and characterization of genes, leading to hereditary muscular dystrophy, atrophy and myotonic diseases
- Universität Würzburg
- Institut für Humangenetik
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- NMD-CHIP: Chip validation and quality assessment (WP5)
- Universität Würzburg
- Institut für Humangenetik
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- GERMANY
- Nordrhein-Westfalen
- BOCHUM
- MYORES: analysis of the signalling pathways controlling hypaxial myogenesis in the avian embryo (2)
- Ruhr-Universität Bochum
- Institut für Anatomie
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- GERMANY
- Nordrhein-Westfalen
- BOCHUM
- MYORES: Identifizierung genetischer Defekte, die mit humanen Myopathien des Fetus assoziiert sind
- Ruhr-Universität Bochum
- Institut für Anatomie
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- Development of an RNA interference-based system for the molecular cell therapy of Myotonic Dystrophy
- Azienda Ospedaliera Universitaria Policlinico di Tor Vergata
- U.O.C. Laboratorio di Genetica Medica
- More details
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- Role of autophagy in muscle diseases
- IRCCS Ospedale Pediatrico Bambino Gesù
- Unità di Malattie Neuromuscolari e Neurodegenerative, Laboratorio di Medicina Molecolare
- More details
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- Characterization of pathways regulating cell cycle and muscle-specific transcription during myogenic differentiation: therapeutical implications for muscle regeneration
- Parco Scientifico Biomedico di Roma San Raffaele
- Laboratorio di Endocrinologia e Metabolismo Molecolare
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- The RAMYD (risk of arrhythmias in Myotonc Dystrophy Type I) study: phase II
- Università Cattolica del Sacro Cuore
- Istituto di Anatomia Umana e Biologia Cellulare
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- Role of Necdin in the differentiation and regeneration of the skeletal muscle: mechanism of action and application to the cell therapy of muscular dystrophy
- Consorzio per la Genetica Molecolare Umana
- Dipartimento di Medicina Sperimentale
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- ITALY
- LOMBARDIA
- SAN DONATO MILANESE
- Validation of a neuromuscular individualized quality of life measure in Italy
- IRCCS Policlinico San Donato
- Clinica Neurologica - Centro per lo Studio delle Malattie Neuromuscolari
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- New mechanisms for the control of TGF-BETA/MYOSTATIN signaling in Muscular Dystrophy
- CNR - Istituto di Neuroscienze
- Dipartimento di Istologia Microbiologia e Biotecnologie Mediche
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- McArm study: development of a motion controlled arm support
- UMC St Radboud - Oost
- Afdeling Revalidatie
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- NETHERLANDS
- Utrecht
- UTRECHT
- GMA - Group medical appointments for neuromuscular patients: To compare group medical appointments (shared medical appointments or group visits) with conventional one to one appointments for patients with a chronic neuromuscular disease in terms of health outcome (quality of life) and costs, an intervention study.
- Piet van Dommelenhuis
- CBO - Kwaliteitsinstituut voor de gezondheidszorg
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- NETHERLANDS
- Zuid-Holland
- LEIDEN
- GMA - Group medical appointments for neuromuscular patients: To compare group medical appointments (shared medical appointments or group visits) with conventional one to one appointments for patients with a chronic neuromuscular disease in terms of health outcome (quality of life) and costs, an intervention study.
- LUMC - Leids Universitair Medisch Centrum
- Afdeling Public Health en Eerstelijnsgeneeskunde
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- Development of new therapies for myotonic dystrophy: in vivo drug discovery
- Instituto Químico de Sarriá
- Grupo de Ingeniería Molecular
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- SPAIN
- Cataluña
- MOLLET DEL VALLÈS
- Development of new therapies for myotonic dystrophy: in vivo drug discovery
- Institut Universitari de Ciència i Tecnologia
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- SPAIN
- Comunidad Valenciana
- BURJASSOT
- New therapeutic targets for myotonic dystrophy: analysis of microRNAs in two animal models of the disease
- Universitat de València. Facultat de Ciencies Biologiques
- Laboratorio de Genómica Traslacional
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- SPAIN
- Comunidad Valenciana
- BURJASSOT
- Development of new therapies for myotonic dystrophy: in vivo drug discovery
- Universitat de València. Facultat de Ciencies Biologiques
- Laboratorio de Genómica Traslacional
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- MYORES: normal and pathological functions of muscle specific proteins
- CBMSO - Centro de Biología Molecular Severo Ochoa
- Análisis Genético y Funcional de la Miogénesis en Drosophila
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- MYORES: muscle patterning, cellular movement and fusion processes
- CBMSO - Centro de Biología Molecular Severo Ochoa
- Análisis Genético y Funcional de la Miogénesis en Drosophila
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- MYORES: normal and pathological functions of muscle specific proteins
- Instituto Cajal (CSIC)
- Análisis Genético de la Regulación Sináptica y Muscular
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- MYORES: muscle patterning, cellular movement and fusion processes
- Instituto Cajal (CSIC)
- Análisis Genético de la Regulación Sináptica y Muscular
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- UNITED KINGDOM
- Greater London
- LONDON
- MYORES: analysis of the signaling pathways controlling hypaxial myogenesis in the avian embryo
- Dental Institute - King's College London
- Department of Cell & Developmental Biology
- More details
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- UNITED KINGDOM
- Greater London
- LONDON
- MYORES: comparison of the mechanisms regulating myogenic specification of trunk versus head muscles
- Dental Institute - King's College London
- Department of Cell & Developmental Biology
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- UNITED KINGDOM
- Greater London
- LONDON
- Explaining and changing adverse illness perceptions in muscle disease by a cognitive behavioural therapy technique
- Guy's Hospital
- Health Psychology Section, Psychology Department, Institute of Psychiatry
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- UNITED KINGDOM
- Greater London
- LONDON
- Study about the control of the efficiency of muscle regeneration and its implications in muscular dystrophies
- School of Biomedical sciences - King's College London
- Randall Division of Cell and Molecular Biophysics
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- UNITED KINGDOM
- Greater London
- LONDON
- Relating satellite cell heterogeneity to stem cell function and its implications in muscular dystrophies
- School of Biomedical sciences - King's College London
- Randall Division of Cell and Molecular Biophysics
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- UNITED KINGDOM
- Norfolk
- NORWICH
- MYORES: study epaxial myogenesis, role of Hedgehog and Wnt signalling in cell fate specification and the molecular basis of their known cooperativity, using animal models
- University of East Anglia
- School of biological sciences, cell and developmental biology
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- UNITED KINGDOM
- Nottinghamshire
- NOTTINGHAM
- Assays for drug discovery in myotonic dystrophy
- Queen's Medical Centre
- Human Genetics Group
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- UNITED KINGDOM
- Shropshire
- OSWESTRY
- A study of buccal cells in Myotonic Dystrophy
- Robert Jones & Agnes Hunt Orthopaedic & District Hospital NHS Trust
- The Centre for Inherited Neuromuscular Disorders
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- UNITED KINGDOM
- South Yorkshire
- SHEFFIELD
- MYORES: study epaxial myogenesis, role of Hedgehog and Wnt signalling in cell fate specification and the molecular basis of their known cooperativity, using animal models
- The University of Sheffield
- Department of Biomedical Science
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- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Long-term application of Poloxamer 188: A potential therapeutic agent in Muscular Dystrophy?
- International Centre for Life
- Institute of Genetic Medicine
- More details
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- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- TREAT-NMD: Accelerating Treatments for Neuromuscular Diseases (coordination)
- International Centre for Life
- Institute of Genetic Medicine
- More details
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- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- NMD-CHIP: societal aspects of the development of targeted DNA-chips for high throughput diagnosis of neuromuscular disorders (WP7)
- Newcastle University
- Policy, Ethics and Life Sciences Research Centre
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