Skip to
  1. Homepage
  2. Research and trials
  3. Research projects
Search by disease/gene

Search by disease/gene

*
(*) mandatory field


 

Other search option(s)

20 matching term(s)

Partnership : Academics = Academics, Industrials = Industrials, Financial investitors = Financial investitors

    • FINLAND
    • Finland
    • HELSINKI
    • Academics
    • Molecular genetics of epilepsy syndromes
    • Folkhälsan
    • The Folkhälsan Institute of Genetics
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • News antiepileptics evaluation in child epilepsy treatment
    • CHU Paris - Hôpital Robert Debré
    • Service de neurologie pédiatrique et des maladies métaboliques
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • RoME : Role of Microglia in Epilepsy
    • Neurophysiology & New Microscopies Laboratory
    • More details
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • Genetics of idiopathic generalized epilepsies
    • Hôpital Henri Gastaut
    • Centre Saint Paul
    • More details
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • EEG, biological and clinical follow-up of rare and serious epileptic child syndrome
    • Hôpital Henri Gastaut
    • Centre Saint Paul
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • IonNeurONet: Molecular diagnosis and exome sequencing in ion channel diseases (project 7)
    • CeGaT GmbH
    • CeGaT GmbH und Praxis für Humangenetik
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • IonNeurONet: Regulation of surface expression and development of bio assays to improve the situation of patients harbouring a mutation leading to transporter defect in channelopathies (project 6)
    • Universitätsklinikum Tübingen
    • Molekulargenetisches Labor
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • IonNeurONet: German Network on neurological and ophthalmological ion channel diseases: Coordination and management (project 1)
    • Universitätsklinikum Tübingen
    • Medizinische Genetik Tübingen
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Differential physiological and pathophysiological role of neuronal voltage gated Na+ channels Nav1.1 (SCN1A) and Nav1.2 (SCN2A)
    • Universitätsklinikum Tübingen
    • Abteilung für Neurologie mit Schwerpunkt Epileptologie
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Ion channel switch and its role for pathogenesis of idiopathic epilepsy syndromes
    • Universitätsklinikum Tübingen
    • Abteilung für Neurologie mit Schwerpunkt Epileptologie
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • EPICURE: Functional genomics and neurobiology of epilepsy: a basis for new therapeutic strategies (coordination)
    • Universitätsklinikum Tübingen
    • Abteilung für Neurologie mit Schwerpunkt Epileptologie
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • IonNeurONet: German Network on neurological and ophthalmological ion channel diseases: Coordination and management (project 1)
    • Universitätsklinikum Tübingen
    • Abteilung für Neurologie mit Schwerpunkt Epileptologie
    • More details
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Excitation-contraction coupling in health and disease: Ion channel diseases - diagnosis, pathogenesis and therapy
    • Universität Ulm
    • Institut für Angewandte Physiologie
    • More details
    • GERMANY
    • Bayern
    • MÜNCHEN
    • 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
    • More details
    • ITALY
    • LOMBARDIA
    • MILANO
    • Functional study of epileptogenic na+ channel mutations in transfected neurons and animal models
    • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
    • Dipartimento di Neurofisiopatologia ed Epilettologia Diagnostica
    • More details
    • ITALY
    • PUGLIA
    • BARI
    • Hereditary chloride channelopathies of skeletal muscle and kidney: from genotype to phenotype and novel pharmacotherapeutical approaches
    • Università degli Studi di Bari
    • Sezione di Farmacologia
    • More details
    • PORTUGAL
    • SUL
    • LISBOA
    • Noninvasive dynamic neuroimaging in epilepsy
    • Instituto Superior Técnico
    • LaSEEB-Evolutionary Systems and Biomedical Engineering Lab
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • NIHR BioResource - Rare Disease: SPEED - Specialist Pathology: Evaluating Exomes in Diagnostics
    • Wellcome Trust/MRC Building
    • Cambridge Institute for Medical Research
    • More details
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Genetic disorders of human brain development
    • Western General Hospital
    • MRC Human Genetics Unit
    • More details
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • NIPSIGEN - Clinical translation of non-invasive prenatal diagnosis (NIPD) for single gene disorders (Health Innovation Challenge Fund)
    • Birmingham Women's NHS Foundation Trust
    • Regional Genetics Unit
    • More details