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14 Resultado(s)
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Proyectos de investigación
SUIZA
Suisse Romande
GENÈVE
Genetic investigations in Children with Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam: A collaborative, prospective, tertiary care center study
Centre Médical Universitaire - CMU
Département de médecine génétique et développement
SUIZA
Suisse Romande
GENÈVE
Genetic investigations in Children with Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam: A collaborative, prospective, tertiary care center study
Hôpital des Enfants - Hôpitaux Universitaires de Genève HUG
Unité de neuropédiatrie
ESPAÑA
Cataluña
BARCELONA
Evaluación de la causalidad de los genes candidatos de NGS en las encefalopatías epilépticas y del desarrollo
Vall d'Hebron Institut de Recerca VHIR
Vall d'Hebron Institut de Recerca
FINLANDIA
Finland
OULU
Novel Diagnostics and Treatment Strategies for Developmental Disorders, Childhood Epilepsies and Movement Disorders
University of Oulu
Biocenter Oulu
ESPAÑA
Galicia
A CORUÑA
Campos magnéticos estáticos como terapia innovadora para la epilepsia refractaria y el síndrome de Dravet; investigación experimental, numérica y clínica
Hospital Materno-Infantil Teresa Herrera
Fundación Profesor Nóvoa Santos
NORUEGA
Østlandet
OSLO
Diet, Gut Microbiota and Epigenetics - Identification of factors associated with successful dietary treatment of epilepsy in children
Oslo University Hospital, Ullevaal
NevSom - Nasjonalt kompetansesenter for nevroutviklingsforstyrrelser og hypersomier
NORUEGA
Østlandet
SANDVIKA
Theraputic drug monitoring of patients across the ages at a referral center
SSE - Spesialistsykehuset for epilepsi, Oslo University Hospital
NK-SE - Nasjonalt kompetansesenter for sjeldne epilepsirelaterte diagnoser
PORTUGAL
SUL
LISBOA
Noninvasive dynamic neuroimaging in epilepsy
Instituto Superior Técnico
LaSEEB-Evolutionary Systems and Biomedical Engineering Lab
REPUBLICA CHECA (LA)
Capital City Prague
PRAHA
Epilepsy genetics: To solve unsolvable cases with combined OMICs tools
University Hospital Motol
Department of Pediatric Neurology
FRANCIA
ILE-DE-FRANCE
PARIS
Neuroglobin gene overexpression: a promising tool for treating a large spectrum of neurological disorders thanks to its ability to safely and sustainably preserve mitochondrial integrity
Institut National de la Santé et de la Recherche Médicale
ITALIA
LAZIO
ROMA
Diverse rare diseases caused by functional dysregulation of Rho GTPase-related proteins
ISS - Istituto Superiore di Sanità
Centro Nazionale Malattie Rare
Proyectos de investigación multicéntricos
- CHU de Lyon HCL - GH Est-Hôpital Femme Mère Enfant
- Service d'epileptologie clinique, des troubles du sommeil et de neurologie fonctionnelle de l'enfant
- University of Antwerp - UA, Campus Drie Eiken
- VIB Department of Molecular Genetics
- The National Hospital For Neurology and Neurosurgery
- Department of Clinical and Experimental Epilepsy
FRANCIA
AUVERGNE-RHONE-ALPES
BRON
NEUROPED: European network of reference for rare paediatric neurological diseases
BELGICA
ANTWERPEN
ANTWERPEN
EuroEPINOMICS: Genetics of rare epilepsy syndromes - RES
REINO UNIDO (EL)
Greater London
LONDON