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Journal Abstract Search

260 related items for PubMed ID: 1544774

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

  • 22. The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness.
    Tremblay F, Laroche RG, De Becker I.
    Vision Res; 1995 Aug; 35(16):2383-93. PubMed ID: 7571473
    [Abstract] [Full Text] [Related]

  • 23. 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]

  • 24. Melanoma-associated paraneoplastic retinopathy: case report and review of the literature.
    Boeck K, Hofmann S, Klopfer M, Ian U, Schmidt T, Engst R, Thirkill CE, Ring J.
    Br J Dermatol; 1997 Sep; 137(3):457-60. PubMed ID: 9349350
    [Abstract] [Full Text] [Related]

  • 25. Rod-cone interactions and analysis of retinal disease.
    Arden GB, Hogg CR.
    Br J Ophthalmol; 1985 Jun; 69(6):404-15. PubMed ID: 3873959
    [Abstract] [Full Text] [Related]

  • 26. Analysis of cone and rod activities of the human retina by the examination of the area effect of total colour blindness and simple congenital night blindness.
    Kamiya S.
    Nihon Ganka Kiyo; 1972 Apr; 23(4):314-22. PubMed ID: 4538005
    [No Abstract] [Full Text] [Related]

  • 27. Rod-cone interactions in night-blinding disease.
    Arden GB.
    Jpn J Ophthalmol; 1987 Apr; 31(1):6-19. PubMed ID: 3498067
    [Abstract] [Full Text] [Related]

  • 28. Dysfunction of transmission in the inner retina: incidence and clinical causes of negative electroretinogram.
    Renner AB, Kellner U, Cropp E, Foerster MH.
    Graefes Arch Clin Exp Ophthalmol; 2006 Nov; 244(11):1467-73. PubMed ID: 16612636
    [Abstract] [Full Text] [Related]

  • 29. Electrophysiological findings in patients with Oguchi's disease.
    Miyake Y, Horiguchi M, Suzuki S, Kondo M, Tanikawa A.
    Jpn J Ophthalmol; 1996 Nov; 40(4):511-9. PubMed ID: 9130055
    [Abstract] [Full Text] [Related]

  • 30. Clinical and immunocytochemical findings in a case of melanoma-associated retinopathy.
    Potter MJ, Thirkill CE, Dam OM, Lee AS, Milam AH.
    Ophthalmology; 1999 Nov; 106(11):2121-5. PubMed ID: 10571347
    [Abstract] [Full Text] [Related]

  • 31. 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; 140(3):279-287. PubMed ID: 31900741
    [Abstract] [Full Text] [Related]

  • 32. Oscillatory potentials and pattern electroretinogram: are they related?
    Litao RE, Miyake Y, Yagasaki K.
    Jpn J Ophthalmol; 1986 Jun; 30(4):402-8. PubMed ID: 3495681
    [Abstract] [Full Text] [Related]

  • 33. ERG characteristics of congenital stationary night blindness.
    Wu D, Xu X, Wu L, Luo T.
    Yan Ke Xue Bao; 1990 Jun; 6(1-2):32-5. PubMed ID: 2101357
    [Abstract] [Full Text] [Related]

  • 34. Duchenne muscular dystrophy: negative scotopic bright-flash electroretinogram but not congenital stationary night blindness.
    Tremblay F, De Becker I, Dooley JM, Riddell DC.
    Can J Ophthalmol; 1994 Dec; 29(6):274-9. PubMed ID: 7834566
    [Abstract] [Full Text] [Related]

  • 35. Melanoma-associated retinopathy: high frequency of subclinical findings in patients with melanoma.
    Pföhler C, Haus A, Palmowski A, Ugurel S, Ruprecht KW, Thirkill CE, Tilgen W, Reinhold U.
    Br J Dermatol; 2003 Jul; 149(1):74-8. PubMed ID: 12890197
    [Abstract] [Full Text] [Related]

  • 36. Cone and rod dysfunction in fundus albipunctatus with RDH5 mutation: an electrophysiological study.
    Niwa Y, Kondo M, Ueno S, Nakamura M, Terasaki H, Miyake Y.
    Invest Ophthalmol Vis Sci; 2005 Apr; 46(4):1480-5. PubMed ID: 15790919
    [Abstract] [Full Text] [Related]

  • 37. 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; 42(11):2728-36. PubMed ID: 11581222
    [Abstract] [Full Text] [Related]

  • 38. 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]

  • 39. Large rod-like photopic signals in a possible new form of congenital night blindness.
    Marmor MF.
    Doc Ophthalmol; 1989 Mar; 71(3):265-9. PubMed ID: 2789128
    [Abstract] [Full Text] [Related]

  • 40. Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.
    Bijveld MM, Florijn RJ, Bergen AA, van den Born LI, Kamermans M, Prick L, Riemslag FC, van Schooneveld MJ, Kappers AM, van Genderen MM.
    Ophthalmology; 2013 Oct; 120(10):2072-81. PubMed ID: 23714322
    [Abstract] [Full Text] [Related]

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