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

231 related items for PubMed ID: 21920492

  • 1. Autofluorescence imaging and spectral-domain optical coherence tomography in incomplete congenital stationary night blindness and comparison with retinitis pigmentosa.
    Chen RW, Greenberg JP, Lazow MA, Ramachandran R, Lima LH, Hwang JC, Schubert C, Braunstein A, Allikmets R, Tsang SH.
    Am J Ophthalmol; 2012 Jan; 153(1):143-54.e2. PubMed ID: 21920492
    [Abstract] [Full Text] [Related]

  • 2. Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations: A Long-Term Follow-up Study.
    Nishiguchi KM, Ikeda Y, Fujita K, Kunikata H, Akiho M, Hashimoto K, Hosono K, Kurata K, Koyanagi Y, Akiyama M, Suzuki T, Kawasaki R, Wada Y, Hotta Y, Sonoda KH, Murakami A, Nakazawa M, Nakazawa T, Abe T.
    Ophthalmology; 2019 Nov; 126(11):1557-1566. PubMed ID: 31257036
    [Abstract] [Full Text] [Related]

  • 3. IMPG2-associated retinitis pigmentosa displays relatively early macular involvement.
    van Huet RA, Collin RW, Siemiatkowska AM, Klaver CC, Hoyng CB, Simonelli F, Khan MI, Qamar R, Banin E, Cremers FP, Theelen T, den Hollander AI, van den Born LI, Klevering BJ.
    Invest Ophthalmol Vis Sci; 2014 May 29; 55(6):3939-53. PubMed ID: 24876279
    [Abstract] [Full Text] [Related]

  • 4. Correlation of fundus autofluorescence with photoreceptor morphology and functional changes in eyes with retinitis pigmentosa.
    Wakabayashi T, Sawa M, Gomi F, Tsujikawa M.
    Acta Ophthalmol; 2010 Aug 29; 88(5):e177-83. PubMed ID: 20491687
    [Abstract] [Full Text] [Related]

  • 5. A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family.
    Vincent A, Wright T, Day MA, Westall CA, Héon E.
    Mol Vis; 2011 Aug 29; 17():3262-70. PubMed ID: 22194652
    [Abstract] [Full Text] [Related]

  • 6. 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 29; 120(10):2072-81. PubMed ID: 23714322
    [Abstract] [Full Text] [Related]

  • 7. Correlation between macular morphology and sensitivity in patients with retinitis pigmentosa and hyperautofluorescent ring.
    Lenassi E, Troeger E, Wilke R, Hawlina M.
    Invest Ophthalmol Vis Sci; 2012 Jan 03; 53(1):47-52. PubMed ID: 22110079
    [Abstract] [Full Text] [Related]

  • 8. Evaluation of Structural Retinal Layer Alterations in Retinitis Pigmentosa.
    Yavuzer K, Citirik M, Yavuzer B.
    Rom J Ophthalmol; 2023 Jan 03; 67(4):326-336. PubMed ID: 38239428
    [Abstract] [Full Text] [Related]

  • 9. Retinal findings in a patient of French ancestry with CABP4-related retinal disease.
    Smirnov VM, Zeitz C, Soumittra N, Audo I, Defoort-Dhellemmes S.
    Doc Ophthalmol; 2018 Apr 03; 136(2):135-143. PubMed ID: 29525873
    [Abstract] [Full Text] [Related]

  • 10. Expanded Retinal Disease Spectrum Associated With Autosomal Recessive Mutations in GUCY2D.
    Stunkel ML, Brodie SE, Cideciyan AV, Pfeifer WL, Kennedy EL, Stone EM, Jacobson SG, Drack AV.
    Am J Ophthalmol; 2018 Jun 03; 190():58-68. PubMed ID: 29559409
    [Abstract] [Full Text] [Related]

  • 11. Novel truncating mutation in CACNA1F in a young male patient diagnosed with optic atrophy.
    Pasutto F, Ekici A, Reis A, Kremers J, Huchzermeyer C.
    Ophthalmic Genet; 2018 Dec 03; 39(6):741-748. PubMed ID: 30260717
    [Abstract] [Full Text] [Related]

  • 12. Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer.
    Al Oreany AA, Al Hadlaq A, Schatz P.
    Graefes Arch Clin Exp Ophthalmol; 2016 Oct 03; 254(10):1951-1956. PubMed ID: 27084085
    [Abstract] [Full Text] [Related]

  • 13. Correlation between B-scan optical coherence tomography, en face thickness map ring and hyperautofluorescent ring in retinitis pigmentosa patients.
    Takahashi VKL, Takiuti JT, Jauregui R, Xu CL, Duong JK, Lima LH, Tsang SH.
    Graefes Arch Clin Exp Ophthalmol; 2019 Aug 03; 257(8):1601-1609. PubMed ID: 31049658
    [Abstract] [Full Text] [Related]

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

  • 15. Congenital Stationary Night Blindness: Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 Patients.
    Katta M, de Guimaraes TAC, Fujinami-Yokokawa Y, Fujinami K, Georgiou M, Mahroo OA, Webster AR, Michaelides M.
    Ophthalmol Retina; 2024 Sep 03; 8(9):932-941. PubMed ID: 38522615
    [Abstract] [Full Text] [Related]

  • 16. Diagnostic imaging in patients with retinitis pigmentosa.
    Mitamura Y, Mitamura-Aizawa S, Nagasawa T, Katome T, Eguchi H, Naito T.
    J Med Invest; 2012 Sep 03; 59(1-2):1-11. PubMed ID: 22449988
    [Abstract] [Full Text] [Related]

  • 17. Novel REEP6 gene mutation associated with autosomal recessive retinitis pigmentosa.
    Lin Y, Xu CL, Velez G, Yang J, Tanaka AJ, Breazzano MP, Mahajan VB, Sparrow JR, Tsang SH.
    Doc Ophthalmol; 2020 Feb 03; 140(1):67-75. PubMed ID: 31538292
    [Abstract] [Full Text] [Related]

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

  • 19. Evaluation of multimodal imaging in carriers of X-linked retinitis pigmentosa.
    Acton JH, Greenberg JP, Greenstein VC, Marsiglia M, Tabacaru M, Theodore Smith R, Tsang SH.
    Exp Eye Res; 2013 Aug 03; 113():41-8. PubMed ID: 23669302
    [Abstract] [Full Text] [Related]

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

    Page: [Next] [New Search]
    of 12.