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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)

CANADA

Colombie-Britannique
VICTORIA

CANADA

Ontario
TORONTO

SPAIN

Madrid
MADRID

Funded by an IRDiRC memberIdentification 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

Funded by an IRDiRC memberA powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US

Multicentric Research projects