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Progetti di ricerca

FRANCIA

BRETAGNE
RENNES

Search for genetic variants modifying human iron homeostasis
CHU de Rennes - Hôpital Pontchaillou
UMR 6290 CNRS "Génomique fonctionnelle intégrée et biomarqueurs", Biogenouest® Plate-forme Genomique Santé

FRANCIA

BRETAGNE
RENNES

Study of penetrance of C282Y homozygocity in hereditary hemochromatosis
CHU de Rennes - Hôpital Pontchaillou
Service des maladies du foie

FRANCIA

OCCITANIE
MONTPELLIER

Hereditary pathology of the red blood cell and of iron metabolism: study of genetic factors interaction
CHU de Montpellier - Hôpital Saint-Eloi
Département d'Hématologie biologique

FRANCIA

OCCITANIE
MONTPELLIER

Study of genes implicated in iron metabolism and clinical expression of hereditary hemochromatosis
CHU de Montpellier - Hôpital Saint-Eloi
Département d'Hématologie biologique

FRANCIA

OCCITANIE
TOULOUSE

Search for genetic factors modifying hemochromatosis penetrance using different approaches like a murine model of the disease
CHU de Toulouse - Hôpital Purpan
Département génétique - maladies humaines et modèles animaux

ITALIA

EMILIA ROMAGNA
MODENA

Finanziato da un ente associato a IRDiRCAnomalie e adattamento metabolico nell'emocromatosi ereditaria: meccanismi e conseguenze della carenza di epcidina
Azienda Ospedaliero - Universitaria di Modena
S.C. di Medicina Interna II

ITALIA

PIEMONTE
TORINO

Finanziato da un ente associato a IRDiRCRuolo delle proteine plasmatiche aptoglobina ed emopexina nella patogenesi dell' emocromatosi (completato)
Azienda Ospedaliero-Universitaria San Giovanni Battista di Torino
Dipartimento di Genetica Biologia e Biochimica

PORTOGALLO

SUL
LISBOA

Non-classical hereditary hemochromatosis and other rare genetic diseases associated with disorders in iron homeostasis
Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
Departamento de Genética

PAESI BASSI

Gelderland
NIJMEGEN

Finanziato da un ente associato a IRDiRCEURENOMICS: European Consortium for High-Throughput Research in Rare Kidney Diseases - NL
Radboudumc - Radboud universitair medisch centrum
Afdeling Fysiologie

PAESI BASSI

Utrecht
UTRECHT

Finanziato da un ente associato a IRDiRCEURENOMICS: European Consortium for High-Throughput Research in Rare Kidney Diseases - NL
UMC Utrecht - Universitair Medisch Centrum Utrecht
Polikliniek Genetica

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCSTaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196

FRANCIA

PAYS DE LA LOIRE
NANTES

Finanziato da un ente associato a IRDiRCFROGH : FRench Regional Origins in Genetics for Health - FR
Institut de Recherche en Santé - Université de Nantes
L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291

GIAPPONE

JAPAN
TOKYO

Finanziato da un ente associato a IRDiRCFormation of integrated omics analysis base of refractory diseases in children and perinatal period
National Center for Child Health and Development
Research Institute

ITALIA

CAMPANIA
NAPOLI

Finanziato da un ente associato a IRDiRCProgramma Telethon per le malattie senza diagnosi
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine

CANADA

Ontario
OTTAWA

Finanziato da un ente associato a IRDiRCEmerging team in rare diseases: achieving the "triple aim" for inborn errors of metabolism
Children's Hospital of Eastern Ontario
Newborn Screening Ontario

CANADA

Ontario
OTTAWA, ONTARIO

Finanziato da un ente associato a IRDiRCEmerging team in rare diseases: achieving the "triple aim" for inborn errors of metabolism
University of Ottawa
Department of Epidemiology and Community Medicine

FRANCIA

HAUTS-DE-FRANCE
LILLE

ID2STOP Orphan : InDividualized Drug Selection Technology for Orphan Patients
Faculté des Sciences Pharmaceutiques et Biologiques de Lille
APTEEUS: le patient au coeur de la découverte de son traitement

ITALIA

LIGURIA
GENOVA

Nuove tecnologie e nuove strategie per lo screening neonatale di massa
IRCCS Istituto G. Gaslini - Ospedale Pediatrico
Laboratorio per lo Studio degli Errori Congeniti del Metabolismo

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCBasic and clinical studies in immune function and metabolism
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

SVEZIA

Stockholms läns landsting
STOCKHOLM

Inborn errors of endocrinology and metabolism
Karolinska Institutet - Solna
Department of Molecular Medicine and Surgery

SVIZZERA

Suisse Romande
LAUSANNE

Clinical Characteristics of Adult Patients With Inborn Errors of Metabolism in French-speaking Switzerland
Centre Hospitalier Universitaire Vaudois CHUV - Hôpital Beaumont -
CMM - Centre des Maladies Moléculaires

Progetti di ricerca multicentrici