x

Pesquisar um projeto de investigação

* (*) campo(s) de preenchimento obrigatório

57 Resultado(s)

Ordenados por

Financiado por um membro do IRDiRC =

Projetos de investigação

FRANCA

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Financiado por um membro do 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

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

ALEMANHA

Baden-Württemberg
TÜBINGEN

Financiado por um membro do 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

ALEMANHA

Niedersachsen
GÖTTINGEN

Financiado por um membro do IRDiRCCMT-NET : Biomarkers, validation of selected outcome measures (CMTNSmod)
Max-Planck-Institut für experimentelle Medizin
Abteilung Neurogenetik

ALEMANHA

Niedersachsen
GÖTTINGEN

Financiado por um membro do IRDiRCCMT-NET: Network for Research on Charcot-Marie-Tooth disease (coordination)
Max-Planck-Institut für experimentelle Medizin
Abteilung Neurogenetik

ALEMANHA

Nordrhein-Westfalen
AACHEN

ALEMANHA

Nordrhein-Westfalen
AACHEN

Financiado por um membro do IRDiRCCMT-NET : Pathomechanisms of CMT: Relevance for human nerve pathology
Universitätsklinikum Aachen
Institut für Neuropathologie

ALEMANHA

Nordrhein-Westfalen
BONN

ALEMANHA

Nordrhein-Westfalen
KÖLN

Financiado por um membro do IRDiRCNEUROMICS: Integrated European Project on Omics Research of Rare Neuromuscular and Neurodegenerative Diseases -DE-
Institut für Humangenetik am Universitätsklinikum Köln
Institut für Humangenetik

ALEMANHA

Nordrhein-Westfalen
MÜNSTER

Financiado por um membro do IRDiRCCMT-NET : Natural history and risk factors during development study in adult CMT patients
Universitätsklinikum Münster
Klinik für Schlafmedizin und Neuromuskuläre Erkrankungen

AUSTRIA

TIROL
INNSBRUCK

Financiado por um membro do IRDiRCCMT-NET : Pregnancy assessment in Charcot-Marie-Tooth (CMT) neuropathy
Medizinische Universität Innsbruck
Zentrum Medizinische Genetik Innsbruck

ESPANHA

Comunidad Valenciana
VALENCIA

Financiado por um membro do 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

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCA resource for mouse models of peripheral neuropathy
Institution: Information not provided - US

FINLANDIA

Finland
HELSINKI

Hereditary neuropathy and spastic paraplegia: new mechanisms, biomarkers and treatment
University of Helsinki
Stem Cells and Metabolism Research Program

FRANCA

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

Financiado por um membro do IRDiRCNeurofilaments in Health and Charcot-Marie-Tooth diseases
Institution: Information not provided - FR

FRANCA

ILE-DE-FRANCE
PARIS

Financiado por um membro do 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"

FRANCA

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"

FRANCA

OCCITANIE
MONTPELLIER

Financiado por um membro do 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

FRANCA

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Financiado por um membro do 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

HUNGRIA

Közép-Magyarország
BUDAPEST

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

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

Financiado por um membro do IRDiRCUpper Limbs evaluation in hereditary NeuropAthies: the ULNA project
Institution: Information not provided - IT

ITALIA

LOMBARDIA
MILANO

Financiado por um membro do IRDiRCCMT national registry: towards definition of standards of care and clinical trials
Fondazione IRCCS Istituto Neurologico "Carlo Besta"
Clinica Neuropatie Degenerative Centrali e Periferiche

ITALIA

LOMBARDIA
MILANO

Financiado por um membro do IRDiRCModulating Neuregulin-1 Signals to Treat Hereditary Demyelinating Neuropathies
IRCCS Ospedale San Raffaele
Divisione di Genetica e Biologia Cellulare

ITALIA

LOMBARDIA
MILANO

Financiado por um membro do IRDiRCNEUROMICS: Integrated European Project on Omics Research of Rare Neuromuscular and Neurodegenerative Diseases - IT
Università degli Studi di Milano - Scienze Farmacologiche e Biomolecolari
Laboratorio di Biologia delle Cellule Staminali

PAISES BAIXOS

Zuid-Holland
LEIDEN

SUECIA

Stockholms läns landsting
ADDRESS: NOT PROVIDED - SE

FRANCA

GRAND-EST
ILLKIRCH-GRAFFENSTADEN

Financiado por um membro do 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

FRANCA

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

FRANCA

PAYS DE LA LOIRE
ANGERS

FRANCA

ILE-DE-FRANCE
PARIS

Financiado por um membro do 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

FRANCA

PAYS DE LA LOIRE
NANTES

Financiado por um membro do 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

Financiado por um membro do IRDiRCTelethon Undiagnosed Disease Program - Revised Proposal
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine

JAPAO

JAPAN
ADDRESS : NOT PROVIDED - JP

JAPAO

JAPAN
ADDRESS : NOT PROVIDED - JP

Projetos de investigação multicêntricos