These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

103 related items for PubMed ID: 22117325

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Wide-field true-colour imaging and clinical characterization of a novel GRK1 mutation in Oguchi disease.
    Ballios BG, Weisbrod D, Kohly R, Muni RH, Wright T, Yan P.
    Doc Ophthalmol; 2020 Oct; 141(2):181-185. PubMed ID: 32146548
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Two novel compound heterozygous SAG mutations in an Italian patient with Oguchi disease: A genetic and multimodal retinal imaging study.
    Pilotto E, Trevisson E, Nacci EB, Longhin E, Guidolin F, Midena E.
    Eur J Ophthalmol; 2022 Nov; 32(6):NP1-NP5. PubMed ID: 34162253
    [Abstract] [Full Text] [Related]

  • 5. Mizuo-Nakamura Phenomena.
    Mittal K, Chawla R.
    Ophthalmic Surg Lasers Imaging Retina; 2016 Nov 01; 47(11):1068. PubMed ID: 27842204
    [Abstract] [Full Text] [Related]

  • 6. Mizuo phenomenon observed by scanning laser ophthalmoscopy in a patient with Oguchi disease.
    Usui T, Ichibe M, Ueki S, Takagi M, Hasegawa S, Abe H, Sekiya K, Nakazawa M.
    Am J Ophthalmol; 2000 Sep 01; 130(3):359-61. PubMed ID: 11020420
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Oguchi disease caused by a homozygous novel SAG splicing alteration associated with the multiple evanescent white dot syndrome: A 15-month follow-up.
    Liu X, Gao L, Wang G, Long Y, Ren J, Fujinami K, Meng X, Li S.
    Doc Ophthalmol; 2020 Dec 01; 141(3):217-226. PubMed ID: 32333190
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Oguchi disease with sectoral retinitis pigmentosa harboring adenine deletion at position 1147 in the arrestin gene.
    Nakamachi Y, Nakamura M, Fujii S, Yamamoto M, Okubo K.
    Am J Ophthalmol; 1998 Feb 01; 125(2):249-51. PubMed ID: 9467455
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. The first case of Oguchi disease, type 2 in a Polish patient with confirmed GRK1 gene mutation.
    Skorczyk-Werner A, Kocięcki J, Wawrocka A, Wicher K, Krawczyńiski MR.
    Klin Oczna; 2015 Feb 01; 117(1):27-30. PubMed ID: 26349155
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. X-linked recessive cone dystrophy with tapetal-like sheen. A newly recognized entity with Mizuo-Nakamura phenomenon.
    Heckenlively JR, Weleber RG.
    Arch Ophthalmol; 1986 Sep 01; 104(9):1322-8. PubMed ID: 3489456
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. A Homozygote Mutation in S-Antigen Visual Arrestin SAG Gene in an Iranian Patient with Oguchi Type One: A Case Report.
    Aryan H, Bahadori A, Farhud DD, Zarif Yeganeh M, Pourkalhor H.
    Iran J Public Health; 2020 May 01; 49(5):995-1000. PubMed ID: 32953689
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.