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13 Result(s)

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    • CANADA
    • Colombie-Britannique
    • VANCOUVER
    • FORGE - Finding of Rare Disease Genes in Canada
    • University of British Columbia
    • Faculty of Medicine
    • More details
    • CANADA
    • Ontario
    • OTTAWA, ONTARIO
    • FORGE - Finding of Rare Disease Genes in Canada
    • University of Ottawa
    • Faculty of Medicine -
    • More details
    • CANADA
    • Québec
    • MONTREAL
    • FORGE - Finding of Rare Disease Genes in Canada
    • Centre hospitalier universitaire Sainte-Justine
    • Pédiatrie
    • More details
    • FRANCE
    • PAYS DE LA LOIRE
    • NANTES
    • Genetics of congenital cardiac conduction defects
    • CHU de Nantes - Hôpital Nord Guillaume et René Laënnec
    • Clinique cardiologique et maladies vasculaires
    • More details
    • FRANCE
    • PAYS DE LA LOIRE
    • NANTES
    • Phenotype profile of congenital cardiac conduction defects
    • CHU de Nantes - Hôpital Nord Guillaume et René Laënnec
    • Clinique cardiologique et maladies vasculaires
    • 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
    • Hessen
    • MARBURG
    • Structure and function of potassium channels of the K2P family in the cardiovascular system (FOR1086)
    • Philipps-Universität Marburg
    • AG Zellphysiologie (Prof. Dr. Dr. Daut)
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Genetic variants in K2P channel genes and monogenetic cardial conduction defects (FOR1086)
    • Universitätsklinikum Münster
    • Institut für Genetik von Herzerkrankungen
    • More details
    • ITALY
    • LAZIO
    • ROMA
    • Molecular basis of conduction defects of the heart
    • Istituto CSS-Mendel
    • Laboratorio di Biologia Molecolare e Citogenetica
    • 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
    • LEBANON
    • Beyrouth
    • BEIRUT
    • Genetic causes of congenital heart diseases in the Lebanese population: screening for mutations in transcription factors implicated in heart development and cardiac function
    • American University of Beirut
    • Département de biochimie
    • More details
    • SWITZERLAND
    • Suisse Alémanique
    • BASEL
    • Genotyping of patients with inherited arrythmias and cardiomyopathies
    • Universitätsspital Basel
    • CardioBiology Research Laboratories
    • More details
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Gene identification in inherited cardiovascular disease
    • The Heart Hospital
    • Centre for Cardiology In The Young
    • More details