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Journal Abstract Search

101 related items for PubMed ID: 12860821

  • 21. Macular dystrophy in a Japanese family with fundus albipunctatus.
    Hotta K, Nakamura M, Kondo M, Ito S, Terasaki H, Miyake Y, Hida T.
    Am J Ophthalmol; 2003 Jun; 135(6):917-9. PubMed ID: 12788147
    [Abstract] [Full Text] [Related]

  • 22. Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatus.
    Driessen CA, Janssen BP, Winkens HJ, Kuhlmann LD, Van Vugt AH, Pinckers AJ, Deutman AF, Janssen JJ.
    Ophthalmology; 2001 Aug; 108(8):1479-84. PubMed ID: 11470705
    [Abstract] [Full Text] [Related]

  • 23. Novel variants in the RDH5 Gene in a Chinese Han family with fundus albipunctatus.
    Qian T, Gong Q, Shen H, Li C, Wang G, Xu X, Schrauwen I, Wang W.
    BMC Ophthalmol; 2022 Feb 11; 22(1):69. PubMed ID: 35148716
    [Abstract] [Full Text] [Related]

  • 24. 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 11; 157(3):558-70.e1-4. PubMed ID: 24246574
    [Abstract] [Full Text] [Related]

  • 25. 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 11; 118(3):233-8. PubMed ID: 18949499
    [Abstract] [Full Text] [Related]

  • 26. 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 11; 25(8):1096-8. PubMed ID: 16340543
    [No Abstract] [Full Text] [Related]

  • 27. Lack of autofluorescence in fundus albipunctatus associated with mutations in RDH5.
    Schatz P, Preising M, Lorenz B, Sander B, Larsen M, Eckstein C, Rosenberg T.
    Retina; 2010 Dec 11; 30(10):1704-13. PubMed ID: 20829743
    [Abstract] [Full Text] [Related]

  • 28. Fundus albipunctatus: novel mutations and phenotypic description of Israeli patients.
    Pras E, Pras E, Reznik-Wolf H, Sharon D, Raivech S, Barkana Y, Abu-Horowitz A, Ygal R, Banin E.
    Mol Vis; 2012 Dec 11; 18():1712-8. PubMed ID: 22815624
    [Abstract] [Full Text] [Related]

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

  • 30. Albipunctate retinopathy with cone dysfunction and no abnormality in the RDH5 or RLBP1 genes.
    Marmor MF, Haeseleer F, Palczewski K.
    Retina; 2003 Aug 11; 23(4):543-6. PubMed ID: 12972770
    [No Abstract] [Full Text] [Related]

  • 31. [Fundus albipunctatus with mutations in the RDH5 gene (clinical case)].
    Zolnikova IV, Kadyshev VV, Marakhonov AV, Zinchenko RA, Cherniak AB, Milash SV, Kogoleva LV, Bobrovskaya YA, Kokoeva NS, Egorova IV, Rogova SY.
    Vestn Oftalmol; 2021 Aug 11; 137(1):68-73. PubMed ID: 33610152
    [Abstract] [Full Text] [Related]

  • 32. Resolution of night blindness in fundus albipunctatus.
    Kranias G, Augsburger JJ, Raymond LA.
    Ann Ophthalmol; 1981 Jul 11; 13(7):871-4. PubMed ID: 6975055
    [Abstract] [Full Text] [Related]

  • 33. Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus.
    Yamamoto H, Simon A, Eriksson U, Harris E, Berson EL, Dryja TP.
    Nat Genet; 1999 Jun 11; 22(2):188-91. PubMed ID: 10369264
    [Abstract] [Full Text] [Related]

  • 34. 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 11; 46(4):1480-5. PubMed ID: 15790919
    [Abstract] [Full Text] [Related]

  • 35. THE TARGET SIGN: A Near Infrared Feature and Multimodal Imaging in a Pluri-Ethnic Cohort with RDH5-Related Fundus Albipunctatus.
    Newman H, Perlman I, Pras E, Rozenberg A, Ben-Yosef T, Iovino C, Simonelli F, Di Iorio V, Rotenstreich Y, Katzburg E, Ehrenberg M, Iglicki M, Zur D.
    Retina; 2022 Jul 01; 42(7):1364-1369. PubMed ID: 35250012
    [Abstract] [Full Text] [Related]

  • 36. Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani families.
    Naz S, Ali S, Riazuddin SA, Farooq T, Butt NH, Zafar AU, Khan SN, Husnain T, Macdonald IM, Sieving PA, Hejtmancik JF, Riazuddin S.
    Br J Ophthalmol; 2011 Jul 01; 95(7):1019-24. PubMed ID: 21447491
    [Abstract] [Full Text] [Related]

  • 37. Novel mutations in the cellular retinaldehyde-binding protein gene (RLBP1) associated with retinitis punctata albescens: evidence of interfamilial genetic heterogeneity and fundus changes in heterozygotes.
    Fishman GA, Roberts MF, Derlacki DJ, Grimsby JL, Yamamoto H, Sharon D, Nishiguchi KM, Dryja TP.
    Arch Ophthalmol; 2004 Jan 01; 122(1):70-5. PubMed ID: 14718298
    [Abstract] [Full Text] [Related]

  • 38. Fundus albipunctatus and other flecked retina syndromes.
    Flynn MF, Bohnert D.
    J Am Optom Assoc; 1999 Sep 01; 70(9):571-80. PubMed ID: 10547972
    [Abstract] [Full Text] [Related]

  • 39. Long-term follow-up of the physiologic abnormalities and fundus changes in fundus albipunctatus.
    Marmor MF.
    Ophthalmology; 1990 Mar 01; 97(3):380-4. PubMed ID: 2336278
    [Abstract] [Full Text] [Related]

  • 40. 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 01; 31(2):66-72. PubMed ID: 20450307
    [Abstract] [Full Text] [Related]

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