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Journal Abstract Search

136 related items for PubMed ID: 33180210

  • 21. Retinal dysfunction in a presymptomatic patient with Huntington's disease.
    Knapp J, VanNasdale DA, Ramsey K, Racine J.
    Doc Ophthalmol; 2018 Jun; 136(3):213-221. PubMed ID: 29691705
    [Abstract] [Full Text] [Related]

  • 22. [Multimodal Approaches for the Analysis of Retinal Functional Disorders―Focusing on Retinal Detachment].
    Terasaki H.
    Nippon Ganka Gakkai Zasshi; 2017 Mar; 121(3):185-231. PubMed ID: 30088405
    [Abstract] [Full Text] [Related]

  • 23. 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; 114(1):134-41. PubMed ID: 17070587
    [Abstract] [Full Text] [Related]

  • 24. 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; 137(2):87-101. PubMed ID: 30051304
    [Abstract] [Full Text] [Related]

  • 25. Optical coherence tomography findings in unilateral peripheral cone dysfunction syndrome: a case report.
    Hasegawa T, Tetsuka S, Yamaguchi A, Kobashi C, Sato T, Tanaka Y, Kakehashi A.
    BMC Ophthalmol; 2019 May 16; 19(1):111. PubMed ID: 31096954
    [Abstract] [Full Text] [Related]

  • 26. [Animal models of human retinal and optic nerve diseases analysed using electroretinography].
    Kondo M.
    Nippon Ganka Gakkai Zasshi; 2010 Mar 16; 114(3):248-78, discussion 279. PubMed ID: 20387538
    [Abstract] [Full Text] [Related]

  • 27. A patient diagnosed with Galloway-Mowat syndrome presenting with a rod-cone functional anomaly with electronegative dark-adapted ERGs.
    Racine J, Golden R.
    Doc Ophthalmol; 2021 Aug 16; 143(1):75-83. PubMed ID: 33548032
    [Abstract] [Full Text] [Related]

  • 28. 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]

  • 29. Cone and rod ERGs in degenerations of central retina.
    Niemeyer G, Demant E.
    Graefes Arch Clin Exp Ophthalmol; 1983 Jul 16; 220(5):201-8. PubMed ID: 6629015
    [Abstract] [Full Text] [Related]

  • 30. Abnormal cone ERGs in a family with congenital nystagmus and photophobia harboring a p.X423Lfs mutation in the PAX6 gene.
    Hood MP, Kerr NC, Smaoui N, Iannaccone A.
    Doc Ophthalmol; 2015 Apr 16; 130(2):157-64. PubMed ID: 25555363
    [Abstract] [Full Text] [Related]

  • 31. Acquired night blindness due to rod dysfunction after long-term hemodialysis.
    Ueno S, Okado S.
    Jpn J Ophthalmol; 2022 Jan 16; 66(1):1-7. PubMed ID: 34741231
    [Abstract] [Full Text] [Related]

  • 32. Acute bilateral peripheral cone system dysfunction.
    Kurimoto T, Kondo M, Nishimura M, Oono S, Tagami Y, Okamoto N, Mimura O.
    Retin Cases Brief Rep; 2008 Jan 16; 2(3):193-5. PubMed ID: 25390083
    [Abstract] [Full Text] [Related]

  • 33. Changes in retinal thickness are correlated with alterations of electroretinogram in eyes with central retinal artery occlusion.
    Shinoda K, Yamada K, Matsumoto CS, Kimoto K, Nakatsuka K.
    Graefes Arch Clin Exp Ophthalmol; 2008 Jul 16; 246(7):949-54. PubMed ID: 18425524
    [Abstract] [Full Text] [Related]

  • 34. Peripheral cone dystrophy: a variant of cone dystrophy with predominant dysfunction in the peripheral cone system.
    Kondo M, Miyake Y, Kondo N, Ueno S, Takakuwa H, Terasaki H.
    Ophthalmology; 2004 Apr 16; 111(4):732-9. PubMed ID: 15051206
    [Abstract] [Full Text] [Related]

  • 35. Electrophysiological and microperimetry changes in vitamin A deficiency retinopathy.
    Saker S, Morales M, Jhittay H, Wen Y, Amoaku W.
    Doc Ophthalmol; 2015 Jun 16; 130(3):231-40. PubMed ID: 25626405
    [Abstract] [Full Text] [Related]

  • 36. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.
    Lines MA, Hébert M, McTaggart KE, Flynn SJ, Tennant MT, MacDonald IM.
    Ophthalmology; 2002 Oct 16; 109(10):1862-70. PubMed ID: 12359607
    [Abstract] [Full Text] [Related]

  • 37. RP cone-rod degeneration.
    Heckenlively JR.
    Trans Am Ophthalmol Soc; 1987 Oct 16; 85():438-70. PubMed ID: 3447340
    [Abstract] [Full Text] [Related]

  • 38. GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel Therapies.
    Bouzia Z, Georgiou M, Hull S, Robson AG, Fujinami K, Rotsos T, Pontikos N, Arno G, Webster AR, Hardcastle AJ, Fiorentino A, Michaelides M.
    Am J Ophthalmol; 2020 Feb 16; 210():59-70. PubMed ID: 31704230
    [Abstract] [Full Text] [Related]

  • 39. Late onset cone dystrophy.
    Langwińska-Wośko E, Szulborski K, Broniek-Kowalik K.
    Doc Ophthalmol; 2010 Jun 16; 120(3):215-8. PubMed ID: 20069340
    [Abstract] [Full Text] [Related]

  • 40. 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 16; 132(2):101-9. PubMed ID: 26996188
    [Abstract] [Full Text] [Related]

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