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Terminated research projects = 
Funded by an IRDiRC member = 
Study involving ERN members in at least two Member States = 
Research projects
GERMANY
Bayern
MÜNCHEN
Patient-specific induced pluripotent stem cell models to elucidate the role of TRP channels in the pathogenesis of CPVT1 and of PFHBI (TRR 152: P17)
Klinikum rechts der Isar der Technischen Universität München
Klinik und Poliklinik für Innere Medizin I
GERMANY
Saarland
HOMBURG
Patient-specific induced pluripotent stem cell models to elucidate the role of TRP channels in the pathogenesis of CPVT1 and of PFHBI (TRR 152: P17)
Universitätsklinikum des Saarlandes
Institut für Molekulare Zellbiologie
GERMANY
Bayern
MÜNCHEN
Characterization of the arrhythmia substrates in hereditary in comparison to non-hereditary arrhythmogenic cardiomyopathy by cardiac magnetic resonance imaging
Helios Klinikum München West
Klinik für Kardiologie und Internistische Intensivmedizin
BELGIUM
ARRONDISSEMENT BRUSSELS-CAPITAL
ADDRESS: NOT PROVIDED - BE
QUALI-NEUROREHAB: Impact of a neuro-cardiac rehabilitation program on the quality of life of children, adolescents and young adults with rare congenital heart disease: the multicentre randomized controlled QUALI-NEUROREHAB trial -BE
Institution: Information not provided - BE
FRANCE
HAUTS-DE-FRANCE
ADDRESS: NOT PROVIDED - FR
QUALI-NEUROREHAB: Impact of a neuro-cardiac rehabilitation program on the quality of life of children, adolescents and young adults with rare congenital heart disease: the multicentre randomized controlled QUALI-NEUROREHAB trial -FR
Institution: Information not provided - FR
FRANCE
PROVENCE-ALPES-COTE D'AZUR
NICE
SGLT2 Inhibitors in Adult Patients With Heart Failure Related to Congenital Heart Disease
Faculté de médecine de Nice Sophia-Antipolis
CHU Nice
GERMANY
Bayern
MÜNCHEN
QUALI-NEUROREHAB: Impact of a neuro-cardiac rehabilitation program on the quality of life of children, adolescents and young adults with rare congenital heart disease: the multicentre randomized controlled QUALI-NEUROREHAB trial - DE
Deutsches Herzzentrum München
Klinik für angeborene Herzfehler und Kinderkardiologie
CANADA
Colombie-Britannique
VICTORIA
Silent Genomes: Reducing health care disparities and improving diagnostic success for children with genetic diseases from Indigenous populations
University of Victoria
Community Genetics Research Program/Island Medical Program
CANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
FRANCE
PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
Modelisation and Therapeutic Approaches for Rare Diseases
Université de médecine Aix-Marseille Université
Centre de Génétique de Marseille (Marseille Medical Genetics - MMG)
SPAIN
Andalucía
SEVILLA
Development of bioinformatic tools for the automatic handling of secondary findings and their use in genetic and pharmacogenetic counseling
Fundación Progreso y Salud
Área de bioinformática clínica
SPAIN
Andalucía
SEVILLA
Development of a repository of genomic analysis workflows
Fundación Progreso y Salud
Área de bioinformática clínica
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Centro de Regulación Genómica
Archivo europeo de genomas y fenomas del CRG
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Clínic de Barcelona
Servicio de Inmunologia
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Universitari Vall d'Hebron
Laboratorio de Genética
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital de la Santa Creu i Sant Pau
Servicio de Genética
SPAIN
Cataluña
ESPLUGUES DE LLOBREGAT
Federated network for functional genomics of undiagnosed and rare diseases, RareFunction
Fundació Sant Joan de Déu - Institut de Recerca Sant Joan de Déu
Grupo de investigación en Neurogenética y Medicina Molecular
SPAIN
Cataluña
ESPLUGUES DE LLOBREGAT
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Sant Joan de Déu Barcelona
Servicio de Laboratorio
SPAIN
Cataluña
L'HOSPITALET DE LLOBREGAT
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Universitari de Bellvitge
Unidad de Genética Molecular
SPAIN
Madrid
MADRID
Identification of new genes causing rare diseases in pediatric patients, searching of genetic pharmacological targets, and drugs discovery, the steps for a personalized medicine
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares
Multicentric Research projects
- Institution: Information not provided - FR
- AP-HP. Centre - Université de Paris - HEGP Hôpital Européen Georges Pompidou
- Thérapie cellulaire en pathologie cardiovasculaire
FRANCE
HAUTS-DE-FRANCE
ADDRESS: NOT PROVIDED - FR
QualiNeuroRehab - Impact of a neurocardiology rehabilitation program on quality of life in children, adolescents, and young adults with rare congenital heart disease
FRANCE
ILE-DE-FRANCE
PARIS