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Funded by an IRDiRC member =

    • Molecular mechanisms of pathogenesis and clinical variability in Norrie disease, a familial syndrome of blindness, deafness and mental retadation and allelic disorders (Coats disease, exsudative vitroretinopathy)
    • Universität Zürich
    • Institüt für Medizinische Molekulargenetik
    • More details
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Phenotype-genotype correlation in hereditary degeneration of the retina and the optic nerve (extended function analysis and differentiation, neuro-ophthalmology, mouse models)
    • Forschungsinstitut für Augenheilkunde
    • Forschungsinstitut der Universitäts-Augenklinik Tübingen
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • HOPE2: Hereditary Retinal Disorders - From Patients Towards Therapies to each project: Translation of novel diagnostics procedures and evaluation of experimental therapies in hereditary retinal disorders (subproject 2)
    • Forschungsinstitut für Augenheilkunde
    • Forschungsinstitut der Universitäts-Augenklinik Tübingen
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Genetics and pathophysiology of glaucoma
    • Forschungsinstitut für Augenheilkunde
    • Molekulargenetisches Labor
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Identification of hereditary causes of glaucoma
    • Forschungsinstitut für Augenheilkunde
    • Molekulargenetisches Labor
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Identification of genes for primary glaucoma (SFB 539)
    • Humangenetisches Institut am Universitätsklinikum Erlangen
    • Humangenetisches Institut
    • More details
    • GERMANY
    • Bayern
    • ERLANGEN
    • Biomorphometrics of the optic nerve : Early diagnosis, reproducible changes (SFB 539)
    • Universitätsklinikum Erlangen - Kopfkliniken
    • Augenklinik
    • More details
    • GERMANY
    • Bayern
    • ERLANGEN
    • Identification of genes for primary glaucoma (SFB 539)
    • Universitätsklinikum Erlangen - Kopfkliniken
    • Augenklinik
    • More details
    • GERMANY
    • Bayern
    • ERLANGEN
    • HOPE2: Hereditary Retinal Disorders - From Patients Towards Therapies: Integrated diagnostics in hereditary retinal disorders (subproject 3)
    • Universitätsklinikum Regensburg
    • Zentrum und Institut für Humangenetik Regensburg
    • More details
    • GERMANY
    • Bayern
    • REGENSBURG
    • Diagnostic and therapy of juvenile cataract and glaucoma
    • Augenklinik des UKGM am Standort Gießen
    • Klinik und Poliklinik für Augenheilkunde
    • More details
    • GERMANY
    • Hessen
    • GIEßEN
    • Diagnosis and therapy of hereditary retinal diseases
    • Augenklinik des UKGM am Standort Gießen
    • Klinik und Poliklinik für Augenheilkunde
    • More details
    • GERMANY
    • Hessen
    • GIEßEN
    • Genotype phenotype correlation of hereditary eye diseases
    • Augenklinik des UKGM am Standort Gießen
    • Klinik und Poliklinik für Augenheilkunde
    • More details
    • GERMANY
    • Hessen
    • GIEßEN
    • Funded by an IRDiRC member
    • NIHR BioResource - Rare Disease: SPEED - Specialist Pathology: Evaluating Exomes in Diagnostics
    • Wellcome Trust/MRC Building
    • Cambridge Institute for Medical Research
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • NIPSIGEN - Clinical translation of non-invasive prenatal diagnosis (NIPD) for single gene disorders (Health Innovation Challenge Fund)
    • Birmingham Women's NHS Foundation Trust
    • Regional Genetics Unit
    • More details
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM