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28 Resultado(s)

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Financiado por um membro do IRDiRC = Membro de uma ERN =

Projetos de investigação

BELGICA

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUXELLES

Treat vascular anomalies
de Duve Institute
Laboratory of Human Genetics

ESPANHA

Madrid
MADRID

Financiado por um membro do IRDiRCClinically and molecularly redefining complex vascular malformations: Evaluation of new genes and new pathologies by massive sequencing
INGEMM - Instituto de Genética Médica y Molecular (IdiPAZ)
Sección de Genómica Estructural y Funcional

ALEMANHA

Baden-Württemberg
STUTTGART

COSS-Registry: Clinical Registry for children, adolescents and adults with Osteosarcoma and Bone Tumors
Klinikum Stuttgart - Standort Olgahospital
COSS (Cooperative OsteoSarkom Studiengruppe) Studienzentrale

ALEMANHA

Bayern
ERLANGEN

Late Effects Surveillance System (LESS) for oncological diseases in children und adolescents
Kinder- und Jugendklinik des Universitätsklinikums Erlangen
Kinder- und Jugendklinik

ESPANHA

Cataluña
ESPLUGUES DE LLOBREGAT

Characterize the behaviours and identify patterns of paediatric rare tumours
Fundació Sant Joan de Déu - Institut de Recerca Sant Joan de Déu
Patients Engagement in Research Area

ESPANHA

Madrid
MADRID

Spanish Academy of Dermatology and Venereology (AEDV) Registry of hemangioma
Academia Española de Dermatología y Venereología
Unidad de investigación de la Fundación Academia Española de Dermatología y Venereología

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCClinical and molecular studies of malformations
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCMolecular studies of malformations
Institution: Information not provided - US

ALEMANHA

Hessen
FRANKFURT AM MAIN

ALEMANHA

Mecklenburg-Vorpommern
GREIFSWALD

Characterisation of somatic and intronic variants in the genes CCM1-3 and of miRNA expression regulated by CCM3
Institut für Humangenetik der Universitätsmedizin Greifswald
Institut für Humangenetik

ALEMANHA

Nordrhein-Westfalen
ESSEN

Evaluation of Video-assisted Instructions of Nasal Self-packing in Patients With HHT
Universitätsklinikum Essen
Klinik für Hals-Nasen und Ohrenheilkunde

BELGICA

ANTWERPEN
ANTWERPEN-EDEGEM

SEC: Sensitivity and Accuracy of Prenatal Diagnosis of Severe Congenital Heart Diseases in the Antwerp Region
University Hospital of Antwerp - UZA
Dienst gynaecologie-verloskunde, Prenatale diagnose

ESPANHA

Castilla - León
SALAMANCA

ESPANHA

Madrid
MADRID

Genetic diagnosis of hereditary hemorrhagic telangiectasia (HHT): the HHT genome
Centro de Investigaciones Biológicas (CSIC)
Biología Celular y Molecular

FRANCA

ILE-DE-FRANCE
BOULOGNE-BILLANCOURT

ITALIA

TOSCANA
SIENA

Mutational and functional genomic study in Vascular Malformations to delineate appropriate therapeutic strategies
Azienda Ospedaliera Universitaria Senese - Policlinico Santa Maria alle Scotte
U.O.C. di Genetica Medica

Projetos de investigação multicêntricos