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Journal Abstract Search

199 related items for PubMed ID: 31900741

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

  • 42. Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation.
    McAnany JJ, Alexander KR, Kumar NM, Ying H, Anastasakis A, Fishman GA.
    Ophthalmic Genet; 2013 Sep; 34(3):167-73. PubMed ID: 23289809
    [Abstract] [Full Text] [Related]

  • 43. Novel biallelic loss-of-function KCNV2 variants in cone dystrophy with supernormal rod responses.
    Kutsuma T, Katagiri S, Hayashi T, Yoshitake K, Iejima D, Gekka T, Kohzaki K, Mizobuchi K, Baba Y, Terauchi R, Matsuura T, Ueno S, Iwata T, Nakano T.
    Doc Ophthalmol; 2019 Jun; 138(3):229-239. PubMed ID: 30877594
    [Abstract] [Full Text] [Related]

  • 44. 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]

  • 45. Flash responses of mouse rod photoreceptors in the isolated retina and corneal electroretinogram: comparison of gain and kinetics.
    Heikkinen H, Vinberg F, Pitkänen M, Kommonen B, Koskelainen A.
    Invest Ophthalmol Vis Sci; 2012 Aug 17; 53(9):5653-64. PubMed ID: 22743325
    [Abstract] [Full Text] [Related]

  • 46. Analysis of retinal structure and function in cone dystrophy with supernormal rod response.
    Abdelkader E, Yasir ZH, Khan AM, Raddadi O, Khandekar R, Alateeq N, Nowilaty S, AlShahrani N, Schatz P.
    Doc Ophthalmol; 2020 Aug 17; 141(1):23-32. PubMed ID: 31960170
    [Abstract] [Full Text] [Related]

  • 47. Digoxin-induced reversible dysfunction of the cone photoreceptors in monkeys.
    Kinoshita J, Iwata N, Kimotsuki T, Yasuda M.
    Invest Ophthalmol Vis Sci; 2014 Feb 10; 55(2):881-92. PubMed ID: 24436189
    [Abstract] [Full Text] [Related]

  • 48. Normal S cone electroretinogram b-wave in Oguchi's disease.
    Yamamoto S, Hayashi M, Takeuchi S, Shirao Y, Kita K, Kawasaki K.
    Br J Ophthalmol; 1997 Dec 10; 81(12):1043-5. PubMed ID: 9497461
    [Abstract] [Full Text] [Related]

  • 49. A phenotype-genotype correlation study of X-linked retinoschisis.
    Vincent A, Robson AG, Neveu MM, Wright GA, Moore AT, Webster AR, Holder GE.
    Ophthalmology; 2013 Jul 10; 120(7):1454-64. PubMed ID: 23453514
    [Abstract] [Full Text] [Related]

  • 50. Aland Island Eye Disease with Retinoschisis in the Clinical Spectrum of CACNA1F-Associated Retinopathy-A Case Report.
    Wyględowska-Promieńska D, Świerczyńska M, Śpiewak D, Pojda-Wilczek D, Tronina A, Dorecka M, Smędowski A.
    Int J Mol Sci; 2024 Mar 02; 25(5):. PubMed ID: 38474172
    [Abstract] [Full Text] [Related]

  • 51. 'On' response defect in paraneoplastic night blindness with cutaneous malignant melanoma.
    Alexander KR, Fishman GA, Peachey NS, Marchese AL, Tso MO.
    Invest Ophthalmol Vis Sci; 1992 Mar 02; 33(3):477-83. PubMed ID: 1544774
    [Abstract] [Full Text] [Related]

  • 52. Congenital stationary night blindness with negative electroretinogram. A new classification.
    Miyake Y, Yagasaki K, Horiguchi M, Kawase Y, Kanda T.
    Arch Ophthalmol; 1986 Jul 02; 104(7):1013-20. PubMed ID: 3488053
    [Abstract] [Full Text] [Related]

  • 53. An electrophysiological follow-up study on acquired unilateral nyctalopia.
    Murayama K, Kawabata H, Adachi-Usami E.
    Eye (Lond); 1999 Oct 02; 13 ( Pt 5)():629-34. PubMed ID: 10696314
    [Abstract] [Full Text] [Related]

  • 54. CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated function.
    Khan NW, Wissinger B, Kohl S, Sieving PA.
    Invest Ophthalmol Vis Sci; 2007 Aug 02; 48(8):3864-71. PubMed ID: 17652762
    [Abstract] [Full Text] [Related]

  • 55. Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness.
    Nakamura M, Ito S, Terasaki H, Miyake Y.
    Invest Ophthalmol Vis Sci; 2001 Jun 02; 42(7):1610-6. PubMed ID: 11381068
    [Abstract] [Full Text] [Related]

  • 56. [Establishment of the concept of new clinical entities--complete and incomplete form of congenital stationary night blindness].
    Miyake Y.
    Nippon Ganka Gakkai Zasshi; 2002 Dec 02; 106(12):737-55; discussion 756. PubMed ID: 12610835
    [Abstract] [Full Text] [Related]

  • 57. Two-color pupillometry in KCNV2 retinopathy.
    Collison FT, Park JC, Fishman GA, Stone EM, McAnany JJ.
    Doc Ophthalmol; 2019 Aug 02; 139(1):11-20. PubMed ID: 30927187
    [Abstract] [Full Text] [Related]

  • 58. 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 02; 50(6):532-536. PubMed ID: 17180528
    [Abstract] [Full Text] [Related]

  • 59. Acquired unilateral night blindness associated with a negative electroretinogram waveform.
    Fishman GA, Alexander KR, Milam AH, Derlacki DJ.
    Ophthalmology; 1996 Jan 02; 103(1):96-104. PubMed ID: 8628566
    [Abstract] [Full Text] [Related]

  • 60. Postreceptoral contributions to the light-adapted ERG of mice lacking b-waves.
    Shirato S, Maeda H, Miura G, Frishman LJ.
    Exp Eye Res; 2008 Jun 02; 86(6):914-28. PubMed ID: 18440505
    [Abstract] [Full Text] [Related]

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