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Projetos de investigação encerrados = Financiado por um membro do IRDiRC = Membro de uma ERN =

Projetos de investigação

ALEMANHA

Sachsen
DRESDEN

Perturbed type I interferon responses in pediatric autoinflammatory diseases with vascular inflammation (TRR 237: Nucleic Acid Immunity B18)
Universitätsklinikum Carl Gustav Carus an der TU Dresden
Klinik und Poliklinik für Kinder- und Jugendmedizin

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

CANADA

Colombie-Britannique
VANCOUVER

Financiado por um membro do IRDiRCChronic childhood vasculitis: Characterizing the individual rare diseases to improve patient outcomes
British Columbia Children's Hospital
Division of pediatric rheumatology

ALEMANHA

Schleswig-Holstein
LÜBECK

Financiado por um membro do IRDiRCFAIRVASC: FAIRVASC - building registry interoperability to inform clinical care -DE
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Klinik für Rheumatologie und Klinische Immunologie

AUSTRIA

WIEN
WIEN

Financiado por um membro do IRDiRCiDysChart: Charting key molecules and mechanisms of human immune Dysregulation
AKH BT 25.3
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases

BELGICA

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

CANADA

Colombie-Britannique
VANCOUVER

Immunological mechanisms in systemic vasculitis
Centre for Health Evaluation and Outcome Sciences (CHEOS)
Department of Nephrology

CANADA

Colombie-Britannique
VICTORIA

CANADA

Ontario
TORONTO

ESPANHA

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

ESPANHA

Cataluña
BARCELONA

ESPANHA

Cataluña
BARCELONA

ESPANHA

Cataluña
BARCELONA

ESPANHA

Cataluña
BARCELONA

Financiado por um membro do IRDiRCAtmospheric monitoring and time series analysis of climate and pollution impact on vasculitis onset - ES
ISGlobal - Instituto de Salud Global de Barcelona
Programa de investigación de Clima y salud

ESPANHA

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

ESPANHA

Madrid
MADRID

Financiado por um membro do 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
Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCA powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US

FRANCA

ILE-DE-FRANCE
PARIS

Financiado por um membro do IRDiRCFAIRVASC: FAIRVASC - building registry interoperability to inform clinical care - FR
AP-HP.Centre - Université de Paris - Hôpital Cochin
Unité fonctionnelle de Médecine interne et centre de référence maladies rares

ITALIA

LAZIO
ROMA

SUECIA

Region Skåne
LUND

SUECIA

Region Skåne
LUND

Bacterial virulence factors, innate immunity and prothrombotic mechanisms in renal disease
Lund University
Department of Clinical Sciences - Division of Pediatrics

SUICA

Suisse Alémanique
RÜSCHLIKON

ALEMANHA

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

ALEMANHA

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

BELGICA

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

ESPANHA

Cataluña
BARCELONA

FINLANDIA

Finland
HELSINKI

Genetics of primary immunodeficiency diseases
HUS - Helsinki University Hospital

FRANCA

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCA

ILE-DE-FRANCE
PARIS

Financiado por um membro do IRDiRCRho GTPases and rare skin diseases
IMAGINE - Institut des Maladies Génétiques
Institut IMAGINE - INSERM U1163

NORUEGA

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

REINO UNIDO

Cambridgeshire
CAMBRIDGE

Financiado por um membro do IRDiRCNIHR BioResource - Rare Disease: PID - Primary Immune Disorders
Addenbrooke's Hospital
Department of Medicine - Renal services

SUECIA

Region Stockholm
HUDDINGE

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

SUICA

Suisse Alémanique
BASEL

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

SUICA

Suisse Alémanique
SCHLIEREN

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

SUICA

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

SUICA

Suisse Alémanique
ZÜRICH

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

ITALIA

LAZIO
ROMA

Financiado por um membro do IRDiRCDiverse rare diseases caused by functional dysregulation of Rho GTPase-related proteins
ISS - Istituto Superiore di Sanità
Centro Nazionale Malattie Rare

Projetos de investigação multicêntricos