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Journal Abstract Search

141 related items for PubMed ID: 3500444

  • 1. Variable expressivity in fundus albipunctatus.
    Margolis S, Siegel IM, Ripps H.
    Ophthalmology; 1987 Nov; 94(11):1416-22. PubMed ID: 3500444
    [Abstract] [Full Text] [Related]

  • 2. Fundus albipunctatus and other flecked retina syndromes.
    Flynn MF, Bohnert D.
    J Am Optom Assoc; 1999 Sep; 70(9):571-80. PubMed ID: 10547972
    [Abstract] [Full Text] [Related]

  • 3. Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture.
    Dryja TP.
    Am J Ophthalmol; 2000 Nov; 130(5):547-63. PubMed ID: 11078833
    [Abstract] [Full Text] [Related]

  • 4. Spectral-domain optical coherence tomography and fundus autofluorescence characteristics in patients with fundus albipunctatus and retinitis punctata albescens.
    Genead MA, Fishman GA, Lindeman M.
    Ophthalmic Genet; 2010 Jun; 31(2):66-72. PubMed ID: 20450307
    [Abstract] [Full Text] [Related]

  • 5. Diagnosis in a patient with fundus albipunctatus and atypical fundus changes.
    Hajali M, Fishman GA, Dryja TP, Sweeney MO, Lindeman M.
    Doc Ophthalmol; 2009 Jun; 118(3):233-8. PubMed ID: 18949499
    [Abstract] [Full Text] [Related]

  • 6. Fundus albipunctatus associated with compound heterozygous mutations in RPE65.
    Schatz P, Preising M, Lorenz B, Sander B, Larsen M, Rosenberg T.
    Ophthalmology; 2011 May; 118(5):888-94. PubMed ID: 21211845
    [Abstract] [Full Text] [Related]

  • 7. A novel Gly35Ser mutation in the RDH5 gene in a Japanese family with fundus albipunctatus associated with cone dystrophy.
    Wada Y, Abe T, Sato H, Tamai M.
    Arch Ophthalmol; 2001 Jul; 119(7):1059-63. PubMed ID: 11448328
    [Abstract] [Full Text] [Related]

  • 8. RDH5 gene mutations and electroretinogram in fundus albipunctatus with or without macular dystrophy: RDH5 mutations and ERG in fundus albipunctatus.
    Nakamura M, Skalet J, Miyake Y.
    Doc Ophthalmol; 2003 Jul; 107(1):3-11. PubMed ID: 12906118
    [Abstract] [Full Text] [Related]

  • 9. [Clinical and genetic findings in a patient with fundus albipunctatus].
    Rüther K, Janssen BP, Kellner U, Janssen JJ, Bohne M, Reimann J, Driessen CA.
    Ophthalmologe; 2004 Feb; 101(2):177-85. PubMed ID: 14991316
    [Abstract] [Full Text] [Related]

  • 10. Disappearance of puncta after uveitis in an eye with fundus albipunctatus.
    Imaizumi M, Tatewaki SY, Kimoto K, Takaki Y, Nakatsuka K, Furushima M, Matsumoto CS, Choshi T.
    Retina; 2005 Dec; 25(8):1096-8. PubMed ID: 16340543
    [No Abstract] [Full Text] [Related]

  • 11. Macular dystrophy in a 9-year-old boy with fundus albipunctatus.
    Nakamura M, Miyake Y.
    Am J Ophthalmol; 2002 Feb; 133(2):278-80. PubMed ID: 11812441
    [Abstract] [Full Text] [Related]

  • 12. Abnormal dark adaptation and rhodopsin kinetics in Sorsby's fundus dystrophy.
    Steinmetz RL, Polkinghorne PC, Fitzke FW, Kemp CM, Bird AC.
    Invest Ophthalmol Vis Sci; 1992 Apr; 33(5):1633-6. PubMed ID: 1559761
    [Abstract] [Full Text] [Related]

  • 13. Fundus albipunctatus: a clinical study of the fundus lesions, the physiologic deficit, and the vitamin A metabolism.
    Marmor MF.
    Doc Ophthalmol; 1977 Jun 30; 43(2):277-302. PubMed ID: 302784
    [No Abstract] [Full Text] [Related]

  • 14. Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 gene.
    Iannaccone A, Tedesco SA, Gallaher KT, Yamamoto H, Charles S, Dryja TP.
    Doc Ophthalmol; 2007 Sep 30; 115(2):111-6. PubMed ID: 17476461
    [Abstract] [Full Text] [Related]

  • 15. [Ultra-widefield imaging of fundus albipunctatus discovered in a 30-year-old woman seen for night blindness].
    Boudousq C, Eid P, Arnould L, Ghezala IB, Bron A, Creuzot-Garcher C, Gabrielle PH.
    J Fr Ophtalmol; 2024 Feb 30; 47(2):103972. PubMed ID: 37872070
    [No Abstract] [Full Text] [Related]

  • 16. Verifying complaints of difficulties in night vision using electroretinography and dark adaptation tests.
    Allon G, Friedrich Y, Mezer E, Itzhaki A, Leibu R, Perlman I.
    Doc Ophthalmol; 2020 Apr 30; 140(2):169-180. PubMed ID: 31621038
    [Abstract] [Full Text] [Related]

  • 17. A form of congenital stationary night blindness with apparent defect of rod phototransduction.
    Peachey NS, Fishman GA, Kilbride PE, Alexander KR, Keehan KM, Derlacki DJ.
    Invest Ophthalmol Vis Sci; 1990 Feb 30; 31(2):237-46. PubMed ID: 2303327
    [Abstract] [Full Text] [Related]

  • 18. Autosomal dominant congenital stationary night blindness and normal fundus with an electronegative electroretinogram.
    Noble KG, Carr RE, Siegel IM.
    Am J Ophthalmol; 1990 Jan 15; 109(1):44-8. PubMed ID: 2297031
    [Abstract] [Full Text] [Related]

  • 19. Cone abnormalities in fundus albipunctatus associated with RDH5 mutations assessed using adaptive optics scanning laser ophthalmoscopy.
    Makiyama Y, Ooto S, Hangai M, Ogino K, Gotoh N, Oishi A, Yoshimura N.
    Am J Ophthalmol; 2014 Mar 15; 157(3):558-70.e1-4. PubMed ID: 24246574
    [Abstract] [Full Text] [Related]

  • 20. A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.
    Zhang Q, Zulfiqar F, Riazuddin SA, Xiao X, Yasmeen A, Rogan PK, Caruso R, Sieving PA, Riazuddin S, Hejtmancik JF.
    Mol Vis; 2005 Nov 14; 11():977-85. PubMed ID: 16319817
    [Abstract] [Full Text] [Related]

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