Search for a research project
Other search option(s)
16 Result(s)
Funded by an IRDiRC member = 
Member of a ERN = 
Research projects
FRANCE
HAUTS-DE-FRANCE
LILLE
Research of genes and mutations involved in ventricle disorders with sudden death risk
CHRU de Lille - Hôpital Albert Calmette
Service de cardiologie
FRANCE
ILE-DE-FRANCE
PARIS
Research of genes and mutations involved in ventricle disorders with sudden death risk
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Service de cardiologie - Rythmologie
FRANCE
ILE-DE-FRANCE
PARIS
Clinical, electrophysiological and genetic aspects of Brugada syndrome
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Service de cardiologie - Rythmologie
FRANCE
ILE-DE-FRANCE
PARIS
Research of genes and mutations involved in ventricle disorders with sudden death risk
Hôpital Necker-Enfants Malades
Cardiologie pédiatrique : Unité médico-chirurgicale de cardiologie congénitale et pédiatrique
FRANCE
PAYS DE LA LOIRE
NANTES
Clinical research on Brugada syndrome
Faculté de médecine de Nantes
Physiopathologie et pharmacologie cellulaire et moléculaire
FRANCE
PAYS DE LA LOIRE
NANTES
Phenotype profile of the Brugada syndrome
Faculté de médecine de Nantes
Physiopathologie et pharmacologie cellulaire et moléculaire
FRANCE
PAYS DE LA LOIRE
NANTES
Genetics of the Brugada syndrome
Faculté de médecine de Nantes
Physiopathologie et pharmacologie cellulaire et moléculaire
SPAIN
Cataluña
BARCELONA
Characterization and risk stratification in Brugada syndrome through the development and validation of novel artificial intelligence model-based approaches for precision medicine
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)
Grupo de investigación en arritmias, resincronización e imágenes cardíacas
SWITZERLAND
Suisse Alémanique
BERN
Co-regulation of cardiac ion channels: focus on the sodium channel Nav1.5
Universität Bern
Institute of Biochemistry and Molecular Medicine (IBMM)
SWITZERLAND
Suisse Italienne
LUGANO
A Novel Approach to Assess Atrial Electrical Abnormalities in Patients with Brugada Syndrome: From the ECG to the Creation of a Patient-Specific Cardiac Model
Cardiocentro Ticino
Cardiologia
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
SPAIN
Madrid
MADRID
Bioinformatics developments based on network and systems biology to identify new candidate genes for rare genetic diseases
Fundación Jiménez Díaz
Área de Genética y Genómica
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
Fundación para la Investigación Biomédica del Hospital Universitario 12 de Octubre
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
A powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US
Multicentric Research projects
- AP-HP. Centre - Université de Paris - HEGP Hôpital Européen Georges Pompidou
- Thérapie cellulaire en pathologie cardiovasculaire
FRANCE
ILE-DE-FRANCE
PARIS