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Journal Abstract Search

273 related items for PubMed ID: 10091368

  • 1. [Syndromic hereditary deafness. Usher's syndrome. Oto-neurologic and genetic factors].
    Espinós C, Pérez-Garrigues H, Beneyto M, Vilela C, Rodrigo O, Nájera C.
    An Otorrinolaringol Ibero Am; 1999; 26(1):83-95. PubMed ID: 10091368
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  • 2. Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease.
    Reiners J, Nagel-Wolfrum K, Jürgens K, Märker T, Wolfrum U.
    Exp Eye Res; 2006 Jul; 83(1):97-119. PubMed ID: 16545802
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  • 3. The usher syndromes.
    Keats BJ, Corey DP.
    Am J Med Genet; 1999 Sep 24; 89(3):158-66. PubMed ID: 10704190
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  • 8. [A case of Usher's syndrome associated with psychotic symptoms: diagnosis and follow-up in a psychiatric unit].
    Viala A, Nicot T, Levy F, Vacheron MN.
    Encephale; 2009 Jun 24; 35(3):286-91. PubMed ID: 19540416
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  • 9. A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.
    Mustapha M, Chouery E, Torchard-Pagnez D, Nouaille S, Khrais A, Sayegh FN, Mégarbané A, Loiselet J, Lathrop M, Petit C, Weil D.
    Hum Genet; 2002 Apr 24; 110(4):348-50. PubMed ID: 11941484
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  • 10. Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.
    Sankila EM, Pakarinen L, Kääriäinen H, Aittomäki K, Karjalainen S, Sistonen P, de la Chapelle A.
    Hum Mol Genet; 1995 Jan 24; 4(1):93-8. PubMed ID: 7711740
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  • 11. Long-Term Outcomes of Cochlear Implantation in Usher Syndrome.
    Fehrmann MLA, Lanting CP, Haer-Wigman L, Yntema HG, Mylanus EAM, Huinck WJ, Pennings RJE.
    Ear Hear; 1995 Jan 24; 45(6):1542-1553. PubMed ID: 38987893
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  • 12. An update on the genetics of usher syndrome.
    Millán JM, Aller E, Jaijo T, Blanco-Kelly F, Gimenez-Pardo A, Ayuso C.
    J Ophthalmol; 2011 Jan 24; 2011():417217. PubMed ID: 21234346
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  • 14. Identification of candidate regions for a novel Usher syndrome type II locus.
    Ben Rebeh I, Benzina Z, Dhouib H, Hadjamor I, Amyere M, Ayadi L, Turki K, Hammami B, Kmiha N, Kammoun H, Hakim B, Charfedine I, Vikkula M, Ghorbel A, Ayadi H, Masmoudi S.
    Mol Vis; 2008 Sep 19; 14():1719-26. PubMed ID: 18806881
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  • 16. Current updates on genetic spectrum of usher syndrome.
    Ullah F, Zeeshan Ali M, Ahmad S, Muzammal M, Khan S, Khan J, Ahmad Khan M.
    Nucleosides Nucleotides Nucleic Acids; 2024 May 08; ():1-24. PubMed ID: 38718411
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  • 17. Identification of a novel locus for a USH3 like syndrome combined with congenital cataract.
    Dad S, Østergaard E, Thykjaer T, Albrectsen A, Ravn K, Rosenberg T, Møller LB.
    Clin Genet; 2010 Oct 08; 78(4):388-97. PubMed ID: 20236115
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  • 18. Usher syndrome: from genetics to pathogenesis.
    Petit C.
    Annu Rev Genomics Hum Genet; 2001 Oct 08; 2():271-97. PubMed ID: 11701652
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  • 20. Three novel mutations and twelve polymorphisms identified in the USH2A gene in Israeli USH2 families.
    Adato A, Weston MD, Berry A, Kimberling WJ, Bonne-Tamir A.
    Hum Mutat; 2000 Apr 08; 15(4):388. PubMed ID: 10738000
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