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Progetti di ricerca

FRANCIA

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Finanziato da un ente associato a IRDiRCHTS screening to identify molecules correcting connexon activity in CMTX disorder
CHU de Marseille - Hôpital de la Timone
Thérapie des Maladies Génétiques

ITALIA

LOMBARDIA
MILANO

Studio di nuove misure di outcome (6MWT e SAM) in pazienti affetti da Charcot Marie Tooth tipo 1A e 1B
Fondazione IRCCS Istituto Neurologico "Carlo Besta"
Clinica Neuropatie Degenerative Centrali e Periferiche

AUSTRIA

TIROL
INNSBRUCK

Finanziato da un ente associato a IRDiRCCMT-NET : Pregnancy assessment in Charcot-Marie-Tooth (CMT) neuropathy
Medizinische Universität Innsbruck
Zentrum Medizinische Genetik Innsbruck

AUSTRIA

WIEN
WIEN

Genetic background of late onset inherited peripheral neuropathies
Allgemeines Krankenhaus der Stadt Wien
Universitätsklinik für Orthopädie

FRANCIA

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

Finanziato da un ente associato a IRDiRCNeurofilaments in Health and Charcot-Marie-Tooth diseases
Institution: Information not provided - FR

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCNeuromics: Integrated European -omics research project for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases - FR
Institut du Cerveau et de la Moelle épinière (ICM) - Hôpital Pitié-Salpêtrière
Equipe "Bases moléculaires, physiopathologie et traitement des maladies neurodégénératives"

FRANCIA

ILE-DE-FRANCE
PARIS

Genetical basis of Charcot-Marie-Tooth disease and hereditary neuropathies
Institut du Cerveau et de la Moelle épinière (ICM) - Hôpital Pitié-Salpêtrière
Equipe "Excitabilité, synapse & pathologies associées"

FRANCIA

OCCITANIE
MONTPELLIER

Finanziato da un ente associato a IRDiRCCMT-NRG : Modulation of Neuregulin signaling as an effective strategy to treat hereditary neuropathies (Charcot-Marie-Tooth disease) - FR
CHU de Montpellier - Hôpital Saint-Eloi
Institut des Neurosciences de Montpellier - INSERM U1051

FRANCIA

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Finanziato da un ente associato a IRDiRCIdentification of novel genes in Charcot-Marie-Tooth disease in lebanese consanguineous families, through homozygous by descent analysis of whole genome sequence data
Faculté de Médecine de la Timone
Centre d'enseignement et de recherche en génétique médicale - INSERM UMR S910

GERMANIA

Baden-Württemberg
TÜBINGEN

Finanziato da un ente associato a IRDiRCNEUROMICS: Integrated European Project on Omics Research of Rare Neuromuscular and Neurodegenerative Diseases -DE-
Institut für Medizinische Genetik und angewandte Genomik Tübingen
Institut für Medizinische Genetik und angewandte Genomik

GERMANIA

Niedersachsen
GÖTTINGEN

Finanziato da un ente associato a IRDiRCCMT-NET : Biomarkers, validation of selected outcome measures (CMTNSmod)
Max-Planck-Institut für experimentelle Medizin
Abteilung Neurogenetik

GERMANIA

Niedersachsen
GÖTTINGEN

Finanziato da un ente associato a IRDiRCCMT-NET: Network for Research on Charcot-Marie-Tooth disease (coordination)
Max-Planck-Institut für experimentelle Medizin
Abteilung Neurogenetik

GERMANIA

Nordrhein-Westfalen
AACHEN

Finanziato da un ente associato a IRDiRCCMT-NET : Pathomechanisms of CMT: Relevance for human nerve pathology
Universitätsklinikum Aachen
Institut für Neuropathologie

GERMANIA

Nordrhein-Westfalen
BONN

GERMANIA

Nordrhein-Westfalen
KÖLN

Finanziato da un ente associato a IRDiRCNEUROMICS: Integrated European Project on Omics Research of Rare Neuromuscular and Neurodegenerative Diseases -DE-
Institut für Humangenetik am Universitätsklinikum Köln
Institut für Humangenetik

GERMANIA

Nordrhein-Westfalen
MÜNSTER

Finanziato da un ente associato a IRDiRCCMT-NET : Natural history and risk factors during development study in adult CMT patients
Universitätsklinikum Münster
Klinik für Schlafmedizin und Neuromuskuläre Erkrankungen

ITALIA

EMILIA ROMAGNA
ADDRESS: NOT PROVIDED - IT

ITALIA

EMILIA ROMAGNA
ADDRESS: NOT PROVIDED - IT

ITALIA

EMILIA ROMAGNA
ADDRESS: NOT PROVIDED - IT

ITALIA

EMILIA ROMAGNA
ADDRESS: NOT PROVIDED - IT

Finanziato da un ente associato a IRDiRCUpper Limbs evaluation in hereditary NeuropAthies: the ULNA project
Institution: Information not provided - IT

ITALIA

LOMBARDIA
MILANO

Finanziato da un ente associato a IRDiRCRegistro nazionale CMT: verso la definizione degli standard di cura e le sperimentazioni cliniche
Fondazione IRCCS Istituto Neurologico "Carlo Besta"
Clinica Neuropatie Degenerative Centrali e Periferiche

ITALIA

LOMBARDIA
MILANO

ITALIA

LOMBARDIA
MILANO

Finanziato da un ente associato a IRDiRCNEUROMICS: progetto europeo integrato di ricerca "omica" sulle malattie neuromuscolari e neurodegenerative - IT
Università degli Studi di Milano - Scienze Farmacologiche e Biomolecolari
Laboratorio di Biologia delle Cellule Staminali

SPAGNA

Comunidad Valenciana
VALENCIA

Finanziato da un ente associato a IRDiRCEnhancing diagnosis, prognosis and therapy of rare neurodegenerative diseases
Centro de Investigación Príncipe Felipe (CIPF)
Laboratorio de Genética y Genómica de Enfermedades Neuromusculares

SPAGNA

Comunidad Valenciana
VALENCIA

Finanziato da un ente associato a IRDiRCHereditary neuropathies in childhood and adolescence: genetic diagnosis and determinants of quality of life
IIS La Fe - Instituto de Investigación Sanitaria La Fe
Grupo de investigación en patología neuromuscular y ataxias

SVEZIA

Stockholms läns landsting
ADDRESS: NOT PROVIDED - SE

UNGHERIA

Közép-Magyarország
BUDAPEST

Genetic epidemiology analysis in hereditary neuropathies
Institute of Genomic Medicine and Rare Disorders, Semmelweis University
Genetics Laboratory

FRANCIA

GRAND-EST
ILLKIRCH-GRAFFENSTADEN

Finanziato da un ente associato a IRDiRCGenCognition: Genetic basis of intellectual disability and other cognitive disorders
Institut de génétique et de biologie moléculaire et cellulaire - IGBMC
Département Médecine translationnelle et neurogénétique

FRANCIA

PAYS DE LA LOIRE
NANTES

In vivo modeling for the genetic diagnosis of intellectual disabilities
CHU de Nantes - Institut de Biologie
Laboratoire de génétique moléculaire

REGNO UNITO; GRAN BRETAGNA

Cambridgeshire
HINXTON

The Deciphering Developmental Disorders (the DDD study)
Wellcome Trust Sanger Institute
DECIPHER

FRANCIA

PAYS DE LA LOIRE
ANGERS

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCSTaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196

FRANCIA

PAYS DE LA LOIRE
NANTES

Finanziato da un ente associato a IRDiRCFROGH : 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

ITALIA

CAMPANIA
NAPOLI

Finanziato da un ente associato a IRDiRCProgramma Telethon per le malattie senza diagnosi
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine

REGNO UNITO; GRAN BRETAGNA

Lothian
EDINBURGH

Genetic disorders of human brain development
Western General Hospital
MRC Human Genetics Unit

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