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15 Ergebnis(se)
Förderung durch ein IRDiRC-Mitglied = 
Forschungsprojekt(e)
DEUTSCHLAND
Mecklenburg-Vorpommern
GREIFSWALD
Mutationsspektrum und klinische Symptomatik bei Patienten mit genetisch bedingten Hämostasestörungen
Institut für Humangenetik der Universitätsmedizin Greifswald
Institut für Humangenetik
FRANKREICH
PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
Input of a multidisciplinary management approach in announcing the diagnosis for young children with serious constitutional hemorrhagic disease and their families
CHU de Marseille - Hôpital de la Timone
Service d'Hématologie Immunologie Oncologie Pédiatrique
ITALIEN
LOMBARDIA
MILANO
RBDD: Rare Bleeding Disorders Database network (coordination)
Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico
Laboratorio di Patologie Molecolari Applicate alla Clinica
FRANKREICH
ILE-DE-FRANCE
PARIS
STaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
FRANKREICH
PAYS DE LA LOIRE
NANTES
FROGH : 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
JAPAN
JAPAN
AICHI
Management ofthe clinical diagnostic centre for rare intractable diseases with genome instability and development of potential therapeutic medicine
Research Institute of Environmental Medicine, Nagoya University
JAPAN
JAPAN
AICHI
Establishment of the Next-generation Muti-omics Clinical Diagnostic Centre for rare intractable diseases with genome instability
Research Institute of Environmental Medicine, Nagoya University
JAPAN
JAPAN
TOKYO
Formation of integrated omics analysis base of refractory diseases in children and perinatal period
National Center for Child Health and Development
Research Institute
KANADA
Ontario
TORONTO
Inherited bone marrow failure syndromes: from genomic discoveries to biology
Hospital for Sick Children, Research Institute
Multizentrische Forschungsprojekte
- INVS - Institut National de Veille Sanitaire
- Département des maladies chroniques et des traumatismes
- Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico
- Laboratorio di Patologie Molecolari Applicate alla Clinica
- Muséum National d'Histoire Naturelle
- Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
- Institut de Recherche en Santé - Université de Nantes
- L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
- IRCCS Ospedale Pediatrico Bambino Gesù - SEDE GIANICOLO
- Servizio Clinico di Consulenza Genetica
- University of British Columbia
- Maternal Infant Child and Youth Research Network
FRANKREICH
ILE-DE-FRANCE
SAINT-MAURICE
FranceCoag: French epidemiological network of coagulopathies due to constitutional coagulation factors defect
ITALIEN
LOMBARDIA
MILANO
RBDD: Rare Bleeding Disorders Database network
FRANKREICH
ILE-DE-FRANCE
PARIS
STaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy
FRANKREICH
PAYS DE LA LOIRE
NANTES
FROGH : FRench Regional Origins in Genetics for Health
ITALIEN
LAZIO
ROMA
UnRareNet: a muticenter collaborative research network for the identification and study of rare undiagnosed patients (completed)
KANADA
Colombie-Britannique
VANCOUVER