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Journal Abstract Search

199 related items for PubMed ID: 31900741

  • 1. 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]

  • 2. A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction.
    Barnes CS, Alexander KR, Fishman GA.
    Ophthalmology; 2002 Mar; 109(3):575-83. PubMed ID: 11874764
    [Abstract] [Full Text] [Related]

  • 3. Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy.
    Hayashi T, Hosono K, Kurata K, Katagiri S, Mizobuchi K, Ueno S, Kondo M, Nakano T, Hotta Y.
    Doc Ophthalmol; 2020 Apr; 140(2):147-157. PubMed ID: 31583501
    [Abstract] [Full Text] [Related]

  • 4. Unilateral negative electroretinogram presenting as photophobia.
    Kido A, Ogino K, Miyake Y, Yanagida K, Kikuchi T, Yoshimura N.
    Doc Ophthalmol; 2016 Aug; 133(1):71-9. PubMed ID: 27245454
    [Abstract] [Full Text] [Related]

  • 5. Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.
    Marmor MF, Zeitz C.
    Doc Ophthalmol; 2018 Aug; 137(1):57-62. PubMed ID: 30051303
    [Abstract] [Full Text] [Related]

  • 6. Rod and cone function in the Nougaret form of stationary night blindness.
    Sandberg MA, Pawlyk BS, Dan J, Arnaud B, Dryja TP, Berson EL.
    Arch Ophthalmol; 1998 Jul; 116(7):867-72. PubMed ID: 9682699
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Differentiation of murine models of "negative ERG" by single and repetitive light stimuli.
    Tanimoto N, Akula JD, Fulton AB, Weber BH, Seeliger MW.
    Doc Ophthalmol; 2016 Apr; 132(2):101-9. PubMed ID: 26996188
    [Abstract] [Full Text] [Related]

  • 9. Photoreceptor and postreceptor responses in congenital stationary night blindness.
    Raghuram A, Hansen RM, Moskowitz A, Fulton AB.
    Invest Ophthalmol Vis Sci; 2013 Jul 10; 54(7):4648-58. PubMed ID: 23761088
    [Abstract] [Full Text] [Related]

  • 10. Recurrent episodes of night blindness in a patient with short bowel syndrome.
    Renner AB, Dietrich-Ntoukas T, Jägle H.
    Doc Ophthalmol; 2015 Dec 10; 131(3):221-30. PubMed ID: 26507840
    [Abstract] [Full Text] [Related]

  • 11. 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 10; 111(1):15-21. PubMed ID: 16502303
    [Abstract] [Full Text] [Related]

  • 12. Phenotypic characterization of complete CSNB in the inbred research beagle: how common is CSNB in research and companion dogs?
    Oh A, Loew ER, Foster ML, Davidson MG, English RV, Gervais KJ, Herring IP, Mowat FM.
    Doc Ophthalmol; 2018 Oct 10; 137(2):87-101. PubMed ID: 30051304
    [Abstract] [Full Text] [Related]

  • 13. Transient electroretinographic abnormalities that mimic those of KCNV2 retinopathy: a case report.
    Kaizuka C, Hayashi T, Mizobuchi K, Kubota M, Ueno S, Nakano T.
    Doc Ophthalmol; 2021 Oct 10; 143(2):221-228. PubMed ID: 33738644
    [Abstract] [Full Text] [Related]

  • 14. Electrophysiological and microperimetry changes in vitamin A deficiency retinopathy.
    Saker S, Morales M, Jhittay H, Wen Y, Amoaku W.
    Doc Ophthalmol; 2015 Jun 10; 130(3):231-40. PubMed ID: 25626405
    [Abstract] [Full Text] [Related]

  • 15. In vivo electroretinographic differentiation of rod, short-wavelength and long/medium-wavelength cone responses in dogs using silent substitution stimuli.
    Mowat FM, Wise E, Oh A, Foster ML, Kremers J.
    Exp Eye Res; 2019 Aug 10; 185():107673. PubMed ID: 31128103
    [Abstract] [Full Text] [Related]

  • 16. Reduction of Rod and Cone Function in 6.5-Year-Old Children Born Extremely Preterm.
    Molnar AEC, Andréasson SO, Larsson EKB, Åkerblom HM, Holmström GE.
    JAMA Ophthalmol; 2017 Aug 01; 135(8):854-861. PubMed ID: 28662245
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 42(11):2728-36. PubMed ID: 11581222
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 46(4):1480-5. PubMed ID: 15790919
    [Abstract] [Full Text] [Related]

  • 19. A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses.
    Hayashi T, Gekka T, Takeuchi T, Goto-Omoto S, Kitahara K.
    Ophthalmology; 2007 Jan 01; 114(1):134-41. PubMed ID: 17070587
    [Abstract] [Full Text] [Related]

  • 20. ERG rod a-wave in Oguchi disease.
    Usui T, Tanimoto N, Ueki S, Takagi M, Hasegawa S, Abe H, Sekiya K, Nakazawa M.
    Vision Res; 2004 Mar 01; 44(5):535-40. PubMed ID: 14680778
    [Abstract] [Full Text] [Related]

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