Parceria : Académicos = 
, Industriais = 
, Investidores financeiros = 
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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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- Collection and characterisation of cases with a small supernumerary marker chomosome with the goal of a genotype phenotype correlation
- Universitätsklinikum Jena
- Molekulare Zytogenetik (FISH Labor)
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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 -
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- FORGE - Finding of Rare Disease Genes in Canada
- Centre hospitalier universitaire Sainte-Justine
- Pédiatrie
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- Analysis of new mutations in families with Charcot-Marie-Tooth disease
- The Cyprus Institute of Neurology and Genetics
- Laboratory of neurology and genetics
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- Genetic characterization of CMT families in Cyprus
- The Cyprus Institute of Neurology and Genetics
- Laboratory of neurology and genetics
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- ESPANHA
- Cataluña
- BARCELONA
- Diagnostic potential and reliability of array-CGH technique in chorionic villi samplings. Detection of cryptic chromosome abnormalities and possible fetoplacental discrepancies
- Hospital Clínico de Barcelona (Edificio Helios III)
- Laboratorio de Citogenética y Genética Clínica
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- ESPANHA
- Comunidad Valenciana
- VALENCIA
- TREAT-CMT: Traslational Research, Experimental Medicine and Therapeutics of Charcot-Marie-Tooth Disease (coordination)
- CIBERER
- Centro de Investigación Biomédica en Red de Enfermedades Raras
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- ESPANHA
- Comunidad Valenciana
- VALENCIA
- Traslational Research and disease mechanisms in hereditary peripheral neuropathies: development of a diagnostic tool for Charcot-Marie-Tooth, investigation of the cellular physiopathology of type 4C and characterization of a new hereditary recurrent neuropathy linked to SMYD4 gene
- Centro de Investigación Príncipe Felipe (CIPF)
- Laboratorio de Genética y Genómica de Enfermedades Neuromusculares
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- ESPANHA
- Comunidad Valenciana
- VALENCIA
- TREAT-CMT: Traslational Research, Experimental Medicine and Therapeutics of Charcot-Marie-Tooth Disease - WP2: Translational genomics and identification of biomarkers for the diagnosis of CMT neuropathy
- Centro de Investigación Príncipe Felipe (CIPF)
- Laboratorio de Genética y Genómica de Enfermedades Neuromusculares
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- ESPANHA
- Comunidad Valenciana
- VALENCIA
- TREAT-CMT: Traslational Research, Experimental Medicine and Therapeutics of Charcot-Marie-Tooth Disease - WP3: Cellular routes, physiopathology and therapeutics of CMT neuropathy associated with mitochondria
- Centro de Investigación Príncipe Felipe (CIPF)
- Laboratorio de Genética y Genómica de Enfermedades Neuromusculares
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- ESPANHA
- Comunidad Valenciana
- VALENCIA
- TREAT-CMT: Traslational Research, Experimental Medicine and Therapeutics of Charcot-Marie-Tooth Disease - WP1: Natural history, phenotyping and clinical research tools
- Hospital Universitario y Politécnico La Fe
- Servicio de Neurología (H. La Fe)
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- ESPANHA
- Comunidad Valenciana
- VALENCIA
- Rationalisation of molecular diagnosis of the Charcot-Marie-Tooth neuropathy
- Instituto de Biomedicina de Valencia (CSIC)
- Unidad de Genética y Medicina Molecular
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- FRANCA
- ILE-DE-FRANCE
- LE KREMLIN BICETRE
- Genotype-phenotype relationships in 1A, 1B and X-linked Charcot-Marie-Tooth diseases
- CHU de Bicêtre
- Laboratoire de génétique moléculaire, pharmacogénétique et hormonologie
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- FRANCA
- ILE-DE-FRANCE
- PARIS
- Search for phenotype modifier genes in Charcot-Marie-Tooth 1A
- CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
- Institut du Cerveau et de la Moëlle épinière
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- FRANCA
- ILE-DE-FRANCE
- PARIS
- Genetical basis of Charcot-Marie-Tooth disease and hereditary neuropathies
- CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
- Institut du Cerveau et de la Moëlle épinière
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- FRANCA
- PROVENCE-ALPES-COTE D'AZUR
- MARSEILLE
- CMTHER: CMT1A phenotype correction by modulating molecules for PMP22 gene expression : role of ascorbic acid and other molecules
- CHU de Marseille - Hôpital de la Timone
- Thérapie des Maladies Génétiques
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- Search for genes and mutations implicated in Charcot-Marie-Tooth disease, type 1
- CHU de Lyon-GH Est - Hospices Civils de Lyon
- UF de neurogénétique moléculaire
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- An in vitro model of myelin protein zero mutations in schwann cells: from pathogenesis to therapy
- Università degli Studi di Genova
- Dipartimento di Neuroscienze Oftalmologia e Genetica
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- A multicenter study to evaluate the effects on Charcot Marie Tooth neuropathy type 1A of a composite tradmill, stretching and proprioceptive exercise (Tre SPE) rehabilitation program
- Università degli Studi di Genova
- Dipartimento di Neuroscienze Oftalmologia e Genetica
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- Role of purinergic receptors in myelination: therapeutic implications for treatment of the peripheral neurophaty Charcot-Marie-Tooth 1A
- Università degli Studi di Genova
- Dipartimento di Neuroscienze Oftalmologia e Genetica
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- Novel outcome measures (6MWT and SAM) for Charcot Marie Tooth type 1A and 1B
- Fondazione IRCCS Istituto Neurologico "Carlo Besta"
- Clinica Neuropatie Degenerative Centrali e Periferiche
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- Development of an instrumented movement analysis protocol for the multitasking analysis of locomotor functions in adult and young patients with Charcot Marie Tooth disease type 1A and 1B
- Fondazione IRCCS Istituto Neurologico "Carlo Besta"
- Clinica Neuropatie Degenerative Centrali e Periferiche
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- A multicenter study to evaluate the effects on Charcot Marie Tooth neuropathy type 1A of a composite tradmill, stretching and proprioceptive exercise (Tre SPE) rehabilitation program
- Fondazione IRCCS Istituto Neurologico "Carlo Besta"
- Clinica Neuropatie Degenerative Centrali e Periferiche
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- Restoring cell-extracellular matrix interactions to rescue tissue degeneration and favor repair in hereditary neuropathies
- IRCCS Ospedale San Raffaele - DIBIT
- Unità di Neurobiologia Cellulare e Molecolare
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- Novel outcome measures for Charcot-Marie-Tooth disease
- A.O.U. Policlinico "G. Martino"
- Dipartimento di Neuroscienze, Scienze Psichiatriche ed Anestesiologiche
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- Study on genetic risk factors in Down Syndrome and other forms of mental retardation
- IRCCS OASI Maria Santissima
- Laboratorio di Citogenetica
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- Effect of beta-amyloid protein on fibroblast survival in patients with Down Syndrome
- IRCCS OASI Maria Santissima
- Laboratorio di Citogenetica
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- Expression of apoptotic genes in patients with 22q11.2 microdeletion
- IRCCS OASI Maria Santissima
- Laboratorio di Genetica Molecolare
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- Novel outcome measures for Charcot-Marie-Tooth disease
- Università degli Studi di Verona
- Laboratorio di Neuromorfologia Dipartimento di Scienze Morfologico-Biomediche
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- A multicenter study to evaluate the effects on charcot-marie-tooth neuropathy type 1a of a composite treadmill, stretching and proprioceptive exercise (trespe) rehabilitation program
- Università degli Studi di Verona
- Laboratorio di Neuromorfologia Dipartimento di Scienze Morfologico-Biomediche
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- Role of the PMP22 gene in the variability of Charcot-Marie-Tooth disease type 1A disease
- Mossakowski Medical Research Centre - Polish Academy of Sciances
- Neuromuscular Unit
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- REINO UNIDO
- Cambridgeshire
- HINXTON
- The Deciphering Developmental Disorders (the DDD study)
- Wellcome Trust Sanger Institute
- DECIPHER
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- REINO UNIDO
- Greater London
- LONDON
- Strengthening hip flexors to improve walking distance in people with Charcot Marie Tooth Disease
- National Hospital for Neurology and Neurosurgery
- MRC Centre for Neuromuscular Disease and Department of Molecular Neurosciences
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