Las enfermedades raras son minoritarias,
pero sus pacientes numerosos

Agentes involucrados : Académicos/-as = , Industriales = , Inversores económicos =

• • ALEMANIA
  • Baden-Württemberg
  • TÜBINGEN
  • Phenotype-genotype correlation in hereditary degeneration of the retina and the optic nerve (extended function analysis and differentiation, neuro-ophthalmology, mouse models)
  • Universität Tübingen
  • Forschungsinstitut für Augenheilkunde
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• • ALEMANIA
  • 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)
  • Universität Tübingen
  • Forschungsinstitut für Augenheilkunde
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• • ALEMANIA
  • Bayern
  • REGENSBURG
  • HOPE2: Hereditary Retinal Disorders - From Patients Towards Therapies: Integrated diagnostics in hereditary retinal disorders (subproject 3)
  • Universitätsklinikum Regensburg
  • Zentrum und Institut für Humangenetik Regensburg
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• • ALEMANIA
  • Hessen
  • GIEßEN
  • Genotype phenotype correlation of hereditary eye diseases
  • Universitätsklinikum Gießen und Marburg GmbH, Standort Gießen
  • Klinik und Poliklinik für Augenheilkunde
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• • ALEMANIA
  • Hessen
  • GIEßEN
  • Diagnosis and therapy of hereditary retinal diseases
  • Universitätsklinikum Gießen und Marburg GmbH, Standort Gießen
  • Klinik und Poliklinik für Augenheilkunde
  • Para más detalles
• • ALEMANIA
  • Saarland
  • HOMBURG
  • Visual impairment and blindness in multiple-handicapped children
  • Universitätsklinikum des Saarlandes
  • AG Kinder- & Neuroophthalmologie
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• • BELGICA
  • OOST-VLAANDEREN
  • GENT
  • 
  • Stickler syndrome: otological and orofacial features in distinct genotypes
  • Ghent University Hospital - UZGent
  • Department of Otorhinolaryngology - UZGent
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• • BELGICA
  • OOST-VLAANDEREN
  • GENT
  • 
  • Stickler syndrome: otological and orofacial features in distinct genotypes
  • Ghent University Hospital - UZGent
  • Center for Medical Genetics Ghent
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• • CANADA
  • Colombie-Britannique
  • VANCOUVER
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of British Columbia
  • Faculty of Medicine
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• • CANADA
  • Ontario
  • OTTAWA, ONTARIO
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of Ottawa
  • Faculty of Medicine -
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• • CANADA
  • Québec
  • MONTREAL
  • FORGE - Finding of Rare Disease Genes in Canada
  • Centre hospitalier universitaire Sainte-Justine
  • Pédiatrie
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• • ESTONIA
  • Tartu
  • TARTU
  • The prevalence and genetic background of hereditary hearing impairment in Estonia
  • Children's Clinic of Tartu University
  • Department of Paediatrics
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• • FRANCIA
  • ILE-DE-FRANCE
  • PARIS
  • Characterization of new genes involved in non-syndromic and syndromic deafness (especially Usher syndrome) and corresponding impairement physiopathology
  • Institut Pasteur
  • Unité de Génétique et physiologie cellulaire
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• • ITALIA
  • VENETO
  • PADOVA
  • Pathogenetic mechanisms and therapeutic perspectives for connexin related hereditary hearing loss
  • Venetian Institute of Molecular Medicine
  • Centro Interdipartimentale per lo Studio dei Segnali Cellulari
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