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Journal Abstract Search

162 related items for PubMed ID: 6604514

  • 21. The hereditary syndrome of congenital deafness and retinitis pigmentosa. (Usher's syndrome).
    Kloepfer HW, Laguaite JK.
    Laryngoscope; 1966 May; 76(5):850-62. PubMed ID: 5937908
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  • 22. Retinitis pigmentosa and progressive hearing loss.
    Karp A, Santore F.
    J Speech Hear Disord; 1983 Aug; 48(3):308-14. PubMed ID: 6621021
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  • 23. An unusual otological manifestation of Usher's syndrome in four siblings.
    Karjalainen S, Teräsvirta M, Kärjä J, Kääriäinen H.
    Clin Genet; 1983 Oct; 24(4):273-9. PubMed ID: 6641004
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  • 24. Polyunsaturated fatty acids are lower in blood lipids of Usher's type I but not Usher's type II.
    Maude MB, Anderson EO, Anderson RE.
    Invest Ophthalmol Vis Sci; 1998 Oct; 39(11):2164-6. PubMed ID: 9761296
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  • 25. The relationship between Usher's syndrome and psychosis with Capgras syndrome.
    Waldeck T, Wyszynski B, Medalia A.
    Psychiatry; 2001 Oct; 64(3):248-55. PubMed ID: 11708050
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  • 32. [Usher's syndrome. A family study - ophthalmological and audiological findings].
    Vinding T, Stage J.
    Ugeskr Laeger; 1984 Jan 09; 146(2):102-4. PubMed ID: 6695463
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  • 33. Usher syndrome clinical types I and II: could ocular symptoms and signs differentiate between the two types?
    Tsilou ET, Rubin BI, Caruso RC, Reed GF, Pikus A, Hejtmancik JF, Iwata F, Redman JB, Kaiser-Kupfer MI.
    Acta Ophthalmol Scand; 2002 Apr 09; 80(2):196-201. PubMed ID: 11952489
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  • 34. [Usher's syndrome (association of familial pigmented retinopathy and deafness) 2 cases in a family].
    Michel M, Cotton JB, Picaud JJ, Lamit J, Destiné F, Freycon F.
    Pediatrie; 1968 Dec 09; 23(8):948-51. PubMed ID: 5311102
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  • 36. A novel IMPDH1 mutation (Arg231Pro) in a family with a severe form of autosomal dominant retinitis pigmentosa.
    Grover S, Fishman GA, Stone EM.
    Ophthalmology; 2004 Oct 09; 111(10):1910-6. PubMed ID: 15465556
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  • 38. Usher's syndrome--a premium on prevention.
    Vernon M.
    Sight Sav Rev; 1969 Oct 09; 39(3):152. PubMed ID: 5310741
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  • 39. Novel mutations in the cellular retinaldehyde-binding protein gene (RLBP1) associated with retinitis punctata albescens: evidence of interfamilial genetic heterogeneity and fundus changes in heterozygotes.
    Fishman GA, Roberts MF, Derlacki DJ, Grimsby JL, Yamamoto H, Sharon D, Nishiguchi KM, Dryja TP.
    Arch Ophthalmol; 2004 Jan 09; 122(1):70-5. PubMed ID: 14718298
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  • 40. Signs of Oguchi Disease and Pigmentary Degeneration from Early in Life.
    Nishiguchi KM, Kunikata H, Nakazawa T.
    Ophthalmology; 2020 Jun 09; 127(6):825. PubMed ID: 32444022
    [No Abstract] [Full Text] [Related]

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