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Journal Abstract Search

180 related items for PubMed ID: 6329990

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. [ERG characteristics of congenital stationary night blindness].
    Wu DZ.
    Zhonghua Yan Ke Za Zhi; 1989 Jul; 25(4):203-5. PubMed ID: 2620613
    [Abstract] [Full Text] [Related]

  • 23. Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type.
    Ruether K, Apfelstedt-Sylla E, Zrenner E.
    Ger J Ophthalmol; 1993 Nov; 2(6):429-35. PubMed ID: 8312830
    [Abstract] [Full Text] [Related]

  • 24.
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  • 25. Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina.
    Mansergh F, Orton NC, Vessey JP, Lalonde MR, Stell WK, Tremblay F, Barnes S, Rancourt DE, Bech-Hansen NT.
    Hum Mol Genet; 2005 Oct 15; 14(20):3035-46. PubMed ID: 16155113
    [Abstract] [Full Text] [Related]

  • 26. Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.
    Scholl HP, Langrová H, Pusch CM, Wissinger B, Zrenner E, Apfelstedt-Sylla E.
    Invest Ophthalmol Vis Sci; 2001 Oct 15; 42(11):2728-36. PubMed ID: 11581222
    [Abstract] [Full Text] [Related]

  • 27.
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  • 28. [The hereditary factor as a criterion for the classification of stationary congenital night blindness (author's transl)].
    Thaler A, Heilig P, Hommer K, Hofbauer R.
    Klin Monbl Augenheilkd; 1981 Oct 15; 179(4):285-7. PubMed ID: 6975855
    [Abstract] [Full Text] [Related]

  • 29. [Effects of cyaninoside chloride and Heleniene on mesopic and scotopic vision in myopia and night blindness].
    Solé P, Rigal D, Peyresblanques J.
    J Fr Ophtalmol; 1984 Oct 15; 7(1):35-9. PubMed ID: 6381579
    [Abstract] [Full Text] [Related]

  • 30. A dominant form of congenital stationary night blindness (adCSNB) in a large Chinese family.
    Liu X, Zhuang S, Hu S, Zhang F, Lin B, Li X, Xu D, Chen SH.
    Ann Hum Genet; 2005 May 15; 69(Pt 3):315-21. PubMed ID: 15845035
    [Abstract] [Full Text] [Related]

  • 31. Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer.
    Ball SL, Powers PA, Shin HS, Morgans CW, Peachey NS, Gregg RG.
    Invest Ophthalmol Vis Sci; 2002 May 15; 43(5):1595-603. PubMed ID: 11980879
    [Abstract] [Full Text] [Related]

  • 32.
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  • 33. Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes.
    Neidhardt J, Barthelmes D, Farahmand F, Fleischhauer JC, Berger W.
    Invest Ophthalmol Vis Sci; 2006 Apr 15; 47(4):1630-5. PubMed ID: 16565402
    [Abstract] [Full Text] [Related]

  • 34.
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  • 35. Electroretinographic abnormalities associated with pregabalin: a case report.
    Ninomiya W, Mizobuchi K, Hayashi T, Okude S, Katagiri S, Kubo A, Masuhara N, Nakano T.
    Doc Ophthalmol; 2020 Jun 15; 140(3):279-287. PubMed ID: 31900741
    [Abstract] [Full Text] [Related]

  • 36.
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  • 37. Reduced synaptic vesicle density and aberrant synaptic localization caused by a splice site mutation in the Rs1h gene.
    Johnson BA, Ikeda S, Pinto LH, Ikeda A.
    Vis Neurosci; 2006 Jun 15; 23(6):887-98. PubMed ID: 17266781
    [Abstract] [Full Text] [Related]

  • 38. Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis.
    Seeliger MW, Biesalski HK, Wissinger B, Gollnick H, Gielen S, Frank J, Beck S, Zrenner E.
    Invest Ophthalmol Vis Sci; 1999 Jan 15; 40(1):3-11. PubMed ID: 9888420
    [Abstract] [Full Text] [Related]

  • 39. [Seeing in the dusk: physiological basis and investigation].
    Friedburg C.
    Klin Monbl Augenheilkd; 2004 Jul 15; 221(7):570-6. PubMed ID: 15273912
    [Abstract] [Full Text] [Related]

  • 40. Diurnal rhythm in the human rod ERG. Relationship to cyclic lighting.
    Birch DG, Sandberg MA, Berson EL.
    Invest Ophthalmol Vis Sci; 1986 Feb 15; 27(2):268-70. PubMed ID: 3943951
    [Abstract] [Full Text] [Related]

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