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Journal Abstract Search

215 related items for PubMed ID: 9888420

  • 41. [Clinical and genetic findings in a patient with fundus albipunctatus].
    Rüther K, Janssen BP, Kellner U, Janssen JJ, Bohne M, Reimann J, Driessen CA.
    Ophthalmologe; 2004 Feb; 101(2):177-85. PubMed ID: 14991316
    [Abstract] [Full Text] [Related]

  • 42. A case of human vitamin A deficiency caused by an inherited defect in retinol-binding protein without clinical symptoms except night blindness.
    Wolf G.
    Nutr Rev; 1999 Aug; 57(8):258-60. PubMed ID: 10518414
    [Abstract] [Full Text] [Related]

  • 43. Improvement of scotopic electroretinograms and night blindness with recovery of serum zinc levels.
    Mochizuki K, Murase H, Imose M, Kawakami H, Sawada A.
    Jpn J Ophthalmol; 2006 Aug; 50(6):532-536. PubMed ID: 17180528
    [Abstract] [Full Text] [Related]

  • 44. Nyctalopia with normal rod function: a suppression of cones by rods.
    Falcao-Reis FM, Hogg CR, Frumkes TE, Arden GB.
    Eye (Lond); 1991 Aug; 5 ( Pt 1)():138-44. PubMed ID: 2060663
    [Abstract] [Full Text] [Related]

  • 45. Altered retinoid distribution in the repeated epilation (Er) mutant mouse.
    Jones AH, Lehman P, Dale BA.
    J Craniofac Genet Dev Biol; 1992 Aug; 12(2):63-75. PubMed ID: 1613075
    [Abstract] [Full Text] [Related]

  • 46. Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance.
    Kabanarou SA, Holder GE, Fitzke FW, Bird AC, Webster AR.
    Br J Ophthalmol; 2004 Aug; 88(8):1018-22. PubMed ID: 15258017
    [Abstract] [Full Text] [Related]

  • 47. Electrophysiological and microperimetry changes in vitamin A deficiency retinopathy.
    Saker S, Morales M, Jhittay H, Wen Y, Amoaku W.
    Doc Ophthalmol; 2015 Jun; 130(3):231-40. PubMed ID: 25626405
    [Abstract] [Full Text] [Related]

  • 48. Muscle expression of human retinol-binding protein (RBP). Suppression of the visual defect of RBP knockout mice.
    Quadro L, Blaner WS, Hamberger L, Van Gelder RN, Vogel S, Piantedosi R, Gouras P, Colantuoni V, Gottesman ME.
    J Biol Chem; 2002 Aug 16; 277(33):30191-7. PubMed ID: 12048218
    [Abstract] [Full Text] [Related]

  • 49. Keratomalacia in a child with familial hypo-retinol-binding proteinemia.
    Matsuo T, Matsuo N, Shiraga F, Koide N.
    Jpn J Ophthalmol; 1988 Aug 16; 32(3):249-54. PubMed ID: 3148050
    [Abstract] [Full Text] [Related]

  • 50. The influence of schistosomiasis on the serum concentrations of retinol and retinol binding protein of a rural population in Liberia.
    Stürchler D, Holzer B, Hanck A, Degrémont A.
    Acta Trop; 1983 Sep 16; 40(3):261-9. PubMed ID: 6138976
    [Abstract] [Full Text] [Related]

  • 51. Vitamin A and interstitial retinol-binding protein in an eye with recessive retinitis pigmentosa.
    Bridges CD, O'Gorman S, Fong SL, Alvarez RA, Berson E.
    Invest Ophthalmol Vis Sci; 1985 May 16; 26(5):684-91. PubMed ID: 4039711
    [Abstract] [Full Text] [Related]

  • 52. No major defect detected in the gene of familial hypo-retinol-binding proteinemia.
    Matsuo T, Noji S, Taniguchi S, Matsuo N.
    Jpn J Ophthalmol; 1990 May 16; 34(3):320-4. PubMed ID: 1981919
    [Abstract] [Full Text] [Related]

  • 53. Improvement in S-cone-mediated visual fields and rod function after correction of vitamin A deficiency.
    Hayashi T, Gekka T, Nakano T, Tsuneoka H.
    Eur J Ophthalmol; 2011 May 16; 21(5):657-60. PubMed ID: 21319138
    [Abstract] [Full Text] [Related]

  • 54. Night blindness with depolarizing pattern of ON/OFF response in electroretinogram: a case report.
    Usui T, Tanimoto N, Ueki S, Miki A, Takagi M, Hasegawa S, Abe H.
    Doc Ophthalmol; 2005 Jul 16; 111(1):15-21. PubMed ID: 16502303
    [Abstract] [Full Text] [Related]

  • 55. Autoradiographic localization of serum retinol-binding protein receptors on the pigment epithelium of dystrophic rat retinas.
    Bok D, Heller J.
    Invest Ophthalmol Vis Sci; 1980 Dec 16; 19(12):1405-14. PubMed ID: 6254901
    [Abstract] [Full Text] [Related]

  • 56. Impaired retinal function and vitamin A availability in mice lacking retinol-binding protein.
    Quadro L, Blaner WS, Salchow DJ, Vogel S, Piantedosi R, Gouras P, Freeman S, Cosma MP, Colantuoni V, Gottesman ME.
    EMBO J; 1999 Sep 01; 18(17):4633-44. PubMed ID: 10469643
    [Abstract] [Full Text] [Related]

  • 57. The first case of Oguchi disease, type 2 in a Polish patient with confirmed GRK1 gene mutation.
    Skorczyk-Werner A, Kocięcki J, Wawrocka A, Wicher K, Krawczyńiski MR.
    Klin Oczna; 2015 Sep 01; 117(1):27-30. PubMed ID: 26349155
    [Abstract] [Full Text] [Related]

  • 58. Functional abnormalities in vincristine-induced night blindness.
    Ripps H, Carr RE, Siegel IM, Greenstein VC.
    Invest Ophthalmol Vis Sci; 1984 Jul 01; 25(7):787-94. PubMed ID: 6329990
    [Abstract] [Full Text] [Related]

  • 59. Photopic abnormalities in congenital stationary nightblindness.
    Krill AE, Martin D.
    Invest Ophthalmol; 1971 Aug 01; 10(8):625-36. PubMed ID: 5315207
    [No Abstract] [Full Text] [Related]

  • 60. Scotopic thresholds and plasma retinol in cystic fibrosis.
    Fulton AB, Hansen RM, Underwood BA, Shwachman H, Barg DC.
    Invest Ophthalmol Vis Sci; 1982 Sep 01; 23(3):364-70. PubMed ID: 7107162
    [Abstract] [Full Text] [Related]

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