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Journal Abstract Search

114 related items for PubMed ID: 4539460

  • 21. Early-onset autosomal dominant retinitis pigmentosa with severe hyperopia.
    Lam BL, Judisch GF.
    Am J Ophthalmol; 1991 Apr 15; 111(4):454-6. PubMed ID: 2012147
    [Abstract] [Full Text] [Related]

  • 22. Clinical and electrophysiological observations on genetic carriers of retinitis pigmentosa in a family (pedigree Tt) showing sex-linked inheritance.
    Imaizumi K, Takahashi R, Tazawa Y, Yamada K, Mita K.
    Adv Exp Med Biol; 1972 Apr 15; 24(0):301-7. PubMed ID: 4671885
    [No Abstract] [Full Text] [Related]

  • 23. [The incidence of Usher's syndrome and its clinical types].
    Bereketoğlu M, Avşar EU, Turan O, Afrashi F, Apaydin F.
    Kulak Burun Bogaz Ihtis Derg; 2002 Apr 15; 9(1):15-20. PubMed ID: 12122620
    [Abstract] [Full Text] [Related]

  • 24. In our parents' shadow, Usher's syndrome.
    Gelbart M.
    Nurs Times; 2002 Apr 15; 94(34):35. PubMed ID: 9791511
    [No Abstract] [Full Text] [Related]

  • 25. [Clinical examinations in Usher's syndrome].
    Lubiński W, Palacz O, Zajaczek S.
    Klin Oczna; 1996 Jan 15; 98(1):55-8. PubMed ID: 9019578
    [Abstract] [Full Text] [Related]

  • 26. [Complicated cataracts in various forms of retinitis pigmentosa. Type and incidence].
    Auffarth GU, Tetz MR, Krastel H, Blankenagel A, Völcker HE.
    Ophthalmologe; 1997 Sep 15; 94(9):642-6. PubMed ID: 9410231
    [Abstract] [Full Text] [Related]

  • 27. Sensorineural deafness: familial incidence and additional defects--study of a school for deaf children.
    Fishman JE, Cristal N.
    Am J Med Sci; 1973 Aug 15; 266(2):111-7. PubMed ID: 4542658
    [No Abstract] [Full Text] [Related]

  • 28. The hereditary syndrome of congenital deafness and retinitis pigmentosa. (Usher's syndrome).
    Kloepfer HW, Laguaite JK.
    Laryngoscope; 1966 May 15; 76(5):850-62. PubMed ID: 5937908
    [No Abstract] [Full Text] [Related]

  • 29. Usher's syndrome type 3 in Finland.
    Pakarinen L, Karjalainen S, Simola KO, Laippala P, Kaitalo H.
    Laryngoscope; 1995 Jun 15; 105(6):613-7. PubMed ID: 7769945
    [Abstract] [Full Text] [Related]

  • 30. Syndrome of congenital high myopia with nyctalopia. Report of findings in 25 families.
    Merin S, Rowe H, Auerbach E, Landau J.
    Am J Ophthalmol; 1970 Oct 15; 70(4):541-7. PubMed ID: 5311788
    [No Abstract] [Full Text] [Related]

  • 31. [Genetic and clinical aspects of Usher's syndrome].
    Cincă D, Pană I, Mănescu M.
    Otorinolaringologie; 1966 Oct 15; 11(1):19-30. PubMed ID: 5938270
    [No Abstract] [Full Text] [Related]

  • 32. [Etiologic problems of hearing disorders in "risk children"].
    Beckmann G.
    HNO; 1969 Aug 15; 17(8):225-9. PubMed ID: 4996331
    [No Abstract] [Full Text] [Related]

  • 33. [Usher's syndrome].
    Gerinec A, Mazanec V.
    Cesk Oftalmol; 1986 May 15; 42(3):174-9. PubMed ID: 3719769
    [No Abstract] [Full Text] [Related]

  • 34. Usher's syndrome: electrophysiological tests of the visual and auditory systems.
    Abraham FA, Cohen D, Sohmer H.
    Doc Ophthalmol; 1977 Dec 30; 44(2):435-44. PubMed ID: 598276
    [Abstract] [Full Text] [Related]

  • 35. Prevalence of foveal lesions in type 1 and type 2 Usher's syndrome.
    Fishman GA, Anderson RJ, Lam BL, Derlacki DJ.
    Arch Ophthalmol; 1995 Jun 30; 113(6):770-3. PubMed ID: 7786220
    [Abstract] [Full Text] [Related]

  • 36. The vitreo-tapeto-retinal degenerations.
    Carr RE, Siegel IM.
    Arch Ophthalmol; 1970 Oct 30; 84(4):436-41 passim. PubMed ID: 5312812
    [No Abstract] [Full Text] [Related]

  • 37. Usher's syndrome.
    Ullal GR, Narayana HS.
    J Indian Med Assoc; 1985 Nov 30; 83(11):381-2. PubMed ID: 3833988
    [No Abstract] [Full Text] [Related]

  • 38. Autosomal inheritance of "senile" retinitis pigmentosa. A report of a family with consanguinity.
    Bonneau D, Kaplan J, Girard G, Dufier JL.
    Clin Genet; 1992 Oct 30; 42(4):199-200. PubMed ID: 1424244
    [Abstract] [Full Text] [Related]

  • 39. The functional syndromes.
    François J.
    Ophthalmologica; 1974 Oct 30; 169(1-3):234-9. PubMed ID: 4547324
    [No Abstract] [Full Text] [Related]

  • 40. IMPG2-associated retinitis pigmentosa displays relatively early macular involvement.
    van Huet RA, Collin RW, Siemiatkowska AM, Klaver CC, Hoyng CB, Simonelli F, Khan MI, Qamar R, Banin E, Cremers FP, Theelen T, den Hollander AI, van den Born LI, Klevering BJ.
    Invest Ophthalmol Vis Sci; 2014 May 29; 55(6):3939-53. PubMed ID: 24876279
    [Abstract] [Full Text] [Related]

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