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Progetti di ricerca

BELGIO

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUXELLES

Treat vascular anomalies
de Duve Institute
Laboratory of Human Genetics

GERMANIA

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

GERMANIA

Bayern
ERLANGEN

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

SPAGNA

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

SPAGNA

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

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCClinical and molecular studies of malformations
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCMolecular studies of malformations
Institution: Information not provided - US

BELGIO

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

FRANCIA

ILE-DE-FRANCE
BOULOGNE-BILLANCOURT

GERMANIA

Hessen
FRANKFURT AM MAIN

GERMANIA

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

GERMANIA

Nordrhein-Westfalen
ESSEN

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

ITALIA

TOSCANA
SIENA

Studio Genomico mutazionale e funzionale nelle Malformazioni Vascolari per delineare appropriate strategie terapeutiche
Azienda Ospedaliera Universitaria Senese - Policlinico Santa Maria alle Scotte
U.O.C. di Genetica Medica

SPAGNA

Cataluña
L'HOSPITALET DE LLOBREGAT

SPAGNA

Madrid
MADRID

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

Progetti di ricerca multicentrici