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Journal Abstract Search

127 related items for PubMed ID: 3785879

  • 1. Nettleship-Falls X-linked ocular albinism with Axenfeld's anomaly. A case report.
    Hayakawa M, Kato K, Nakajima A, Yoshiike T, Ogawa H.
    Ophthalmic Paediatr Genet; 1986 Aug; 7(2):109-14. PubMed ID: 3785879
    [Abstract] [Full Text] [Related]

  • 2. [A Japanese family of Nettleship Falls X-linked ocular albinism].
    Hayakawa M, Kanai A, Kato K, Nakajima A, Takamori K.
    Nippon Ganka Gakkai Zasshi; 1990 Dec; 94(12):1181-7. PubMed ID: 2082739
    [Abstract] [Full Text] [Related]

  • 3. Macromelanosomes in X-linked ocular albinism.
    Garner A, Jay BS.
    Histopathology; 1980 May; 4(3):243-54. PubMed ID: 7390409
    [Abstract] [Full Text] [Related]

  • 4. [Studies of X-linked recessive ocular albinism of the Nettleship-Falls type--with special reference to the association of megalocornea].
    Awaya S, Tsunekawa F, Koizumi E, Miyake Y, Yokoyama K.
    Nippon Ganka Gakkai Zasshi; 1988 Jan; 92(1):146-50. PubMed ID: 3389256
    [No Abstract] [Full Text] [Related]

  • 5. X-Linked ocular albinism; Nettleship-Falls ocular albinism.
    Booth AV, Soldano AC, Levine J, Pomeranz M.
    Dermatol Online J; 2008 May 15; 14(5):4. PubMed ID: 18627740
    [Abstract] [Full Text] [Related]

  • 6. Forsius-Eriksson syndrome: its relation to the Nettleship-Falls X-linked ocular albinism.
    O'Donnell FE, Green WR, McKusick VA, Forsius H, Eriksson AW.
    Clin Genet; 1980 Jun 15; 17(6):403-8. PubMed ID: 7398111
    [Abstract] [Full Text] [Related]

  • 7. X-linked ocular albinism: relative value of skin biopsy, iris transillumination and funduscopy in identifying affected males and carriers.
    Cortin P, Tremblay M, Lemagne JM.
    Can J Ophthalmol; 1981 Jul 15; 16(3):121-3. PubMed ID: 7296358
    [Abstract] [Full Text] [Related]

  • 8. X-linked ocular albinism. An oculocutaneous macromelanosomal disorder.
    O'Donnell FE, Hambrick GW, Green WR, Iliff WJ, Stone DL.
    Arch Ophthalmol; 1976 Nov 15; 94(11):1883-92. PubMed ID: 985163
    [Abstract] [Full Text] [Related]

  • 9. X-linked ocular albinism in Blacks. Ocular albinism cum pigmento.
    O'Donnell FE, Green WR, Fleischman JA, Hambrick GW.
    Arch Ophthalmol; 1978 Jul 15; 96(7):1189-92. PubMed ID: 666626
    [Abstract] [Full Text] [Related]

  • 10. Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysis.
    Bergen AA, Schuurman EJ, van den Born LI, Samanns C, van Dorp DB, Pinckers AJ, Bakker E, van Ommen GJ, Gal A, Bleeker-Wagemakers EM.
    Clin Genet; 1992 Mar 15; 41(3):135-8. PubMed ID: 1348665
    [Abstract] [Full Text] [Related]

  • 11. Aland eye disease: no albino misrouting.
    van Dorp DB, Eriksson AW, Delleman JW, van Vliet AG, Collewijn H, van Balen AT, Forsius HR.
    Clin Genet; 1985 Dec 15; 28(6):526-31. PubMed ID: 4075563
    [Abstract] [Full Text] [Related]

  • 12. Genetic studies of ocular albinism in a large Virginia kindred.
    Szymanski KA, Boughman JA, Nance WE, Olansky DC, Weinberg RS.
    Ann Ophthalmol; 1984 Feb 15; 16(2):183-5, 188-91, 194-6 passim. PubMed ID: 6703591
    [Abstract] [Full Text] [Related]

  • 13. Macromelanosomes in X-linked ocular albinism (XLOA).
    Yoshiike T, Manabe M, Hayakawa M, Ogawa H.
    Acta Derm Venereol; 1985 Feb 15; 65(1):66-9. PubMed ID: 2578709
    [Abstract] [Full Text] [Related]

  • 14. X-linked ocular albinism: a family containing a manifesting heterozygote, and an affected male married to a female with autosomal recessive ocular albinism.
    Jaeger C, Jay B.
    Hum Genet; 1981 Feb 15; 56(3):299-304. PubMed ID: 7239514
    [Abstract] [Full Text] [Related]

  • 15. The familial association of neurofibromatosis, peroneal muscular atrophy, congenital deafness, partial albinism, and Axenfeld's defect.
    Bradley WG, Richardson J, Frew IJ.
    Brain; 1974 Sep 15; 97(3):521-32. PubMed ID: 4213898
    [No Abstract] [Full Text] [Related]

  • 16. Axenfeld's anomaly associated with Down's syndrome.
    Stokes DW, Parrish CM.
    Cornea; 1992 Mar 15; 11(2):163-4. PubMed ID: 1533830
    [Abstract] [Full Text] [Related]

  • 17. Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis.
    Bergen AA, Samanns C, Van Dorp DB, Ferguson-Smith MA, Gal A, Bleeker-Wagemakers EM.
    Ophthalmic Paediatr Genet; 1990 Sep 15; 11(3):165-70. PubMed ID: 2280973
    [Abstract] [Full Text] [Related]

  • 18. Genetic counselling in X-linked ocular albinism: clinical features of the carrier state.
    Charles SJ, Moore AT, Grant JW, Yates JR.
    Eye (Lond); 1992 Sep 15; 6 ( Pt 1)():75-9. PubMed ID: 1426406
    [Abstract] [Full Text] [Related]

  • 19. X linked ocular albinism in Japanese patients.
    Shiono T, Tsunoda M, Chida Y, Nakazawa M, Tamai M.
    Br J Ophthalmol; 1995 Feb 15; 79(2):139-43. PubMed ID: 7696233
    [Abstract] [Full Text] [Related]

  • 20. Oculocutaneous Albinism associated with Axenfeld's Anomaly: Three case reports.
    Keshav BR, Mohammed MJ, Mahmood N.
    Sultan Qaboos Univ Med J; 2010 Apr 15; 10(1):111-3. PubMed ID: 21509091
    [Abstract] [Full Text] [Related]

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