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Financé par un membre IRDiRC = Membre d'un ERN =

Projets de recherche

BELGIQUE

OOST-VLAANDEREN
GENT

Financé par un membre IRDiRCImmunAID: Consortium du projet Immunome pour les troubles auto-inflammatoires - BE
VIB headquarters
VIB (vlaams instituut voor biotechnologie) headquarters

BELGIQUE

VLAAMS BRABANT
LEUVEN

Financé par un membre IRDiRCImmunAID: Consortium du projet Immunome pour les troubles auto-inflammatoires - BE
UZ Leuven - Campus Gasthuisberg
Pediatric Rheumatology

ETATS-UNIS

Washington
ADDRESS: NOT PROVIDED - US

AUTRICHE

WIEN
WIEN

Financé par un membre IRDiRCiDysChart: Charting key molecules and mechanisms of human immune Dysregulation
AKH BT 25.3
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases

BELGIQUE

OOST-VLAANDEREN
GENT

Unraveling pathophysiologic and genetic causes of primary immune deficiencies with a focus on antibody disorders (common variable immunodeficiency= CVID) and disorders of anti-fungal immunity (chronic mucocutaneous candidiasis = CMC)
PID research lab (PIRL), UZ Gent - MRBII - Entrance 38
Center for Primary Immunodeficiencies Ghent, Jeffrey Modell Foundation diagnostic and research center

CANADA

Colombie-Britannique
VICTORIA

CANADA

Ontario
TORONTO

ESPAGNE

Cataluña
BARCELONA

ESPAGNE

Madrid
MADRID

Financé par un membre IRDiRCIdentification 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

ETATS-UNIS

Washington
ADDRESS: NOT PROVIDED - US

Financé par un membre IRDiRCA powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US

FINLANDE

Finland
HELSINKI

Genetics of primary immunodeficiency diseases
HUS - Helsinki University Hospital

ITALIE

LAZIO
ROMA

NORVEGE

Østlandet
OSLO

Functional consequences of genetic variations in primary immunodeficiencies and immune dysregulation (FUNPID)
Oslo Universitetssykehus HF, Rikshospitalet
Nasjonal behandlingstjeneste for screening av nyfødte og avansert laboratoriediagnostikk ved medfødte stoffskiftesykdommer

ROYAUME-UNI

Cambridgeshire
CAMBRIDGE

Financé par un membre IRDiRCNIHR BioResource - Rare Disease: PID - Primary Immune Disorders
Addenbrooke's Hospital
Department of Medicine - Renal services

SUEDE

Region Stockholm
HUDDINGE

Genetic basis of immunodeficiency diseases
Karolinska Institutet - Huddinge
Department of laboratory medicine

SUISSE

Suisse Alémanique
BASEL

The role of ZNF74 in the generation and maintenance of immunological memory
Universitätsspital Basel
Departement Biomedizin

SUISSE

Suisse Alémanique
SCHLIEREN

Pathophysiology of Inborn Immunodeficiencies
Institute for Regenerative Medicine
Department Gene and Cell Therapy

SUISSE

Suisse Alémanique
SCHLIEREN

Towards Identification of New Inborn Errors of Immunity by Whole Exome/Genome Sequencing
Institute for Regenerative Medicine
Department Gene and Cell Therapy

SUISSE

Suisse Alémanique
ZÜRICH

Genetic Study of Immunodeficiency: Search for New Genetic Causes for Primary Immunodeficiencies
Universitäts - Kinderspital Zürich - Eleonorenstiftung
Immunologie

ALLEMAGNE

Bayern
GARMISCH-PARTENKIRCHEN

The importance of motion diagnostics to promote early physical activity in children with rheumatic diseases
Kinderklinik Garmisch-Partenkirchen gGmbH
Deutsches Zentrum für Kinder- und Jugendrheumatologie

ALLEMAGNE

Nordrhein-Westfalen
SANKT AUGUSTIN

Depressive symptoms and association with disease activity, pain and disability in juvenile patients with chronic rheumatic diseases
Asklepios Kinderklinik Sankt Augustin GmbH
Abteilung für Allgemeine Kinder- und Jugendmedizin

ITALIE

LAZIO
ROMA

Financé par un membre IRDiRCDiverse rare diseases caused by functional dysregulation of Rho GTPase-related proteins
ISS - Istituto Superiore di Sanità
Centro Nazionale Malattie Rare

Projets de recherche multicentriques