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22. Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy. Birch DG; Anderson JL; Fish GE Ophthalmology; 1999 Feb; 106(2):258-68. PubMed ID: 9951474 [TBL] [Abstract][Full Text] [Related]
23. Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogram. Ben Salah S; Kamei S; Sénéćhal A; Lopez S; Bazalgette C; Bazalgette C; Eliaou CM; Zanlonghi X; Hamel CP Am J Ophthalmol; 2008 Jun; 145(6):1099-106. PubMed ID: 18400204 [TBL] [Abstract][Full Text] [Related]
24. The phenotype of early-onset retinal degeneration in persons with RDH12 mutations. Schuster A; Janecke AR; Wilke R; Schmid E; Thompson DA; Utermann G; Wissinger B; Zrenner E; Gal A Invest Ophthalmol Vis Sci; 2007 Apr; 48(4):1824-31. PubMed ID: 17389517 [TBL] [Abstract][Full Text] [Related]
25. [Bio-electric tests in tapeto-retinal peripheral degeneration]. François J; De Rouck A Bull Soc Belge Ophtalmol; 1974; 166(2):504-16. PubMed ID: 4433950 [No Abstract] [Full Text] [Related]
26. [Study of a family with cone degeneration]. Malbrel PH; Hache JC; Malbrel C Bull Soc Ophtalmol Fr; 1976; 76(7-8):747-51. PubMed ID: 1088506 [No Abstract] [Full Text] [Related]
27. High-resolution retinal imaging of cone-rod dystrophy. Wolfing JI; Chung M; Carroll J; Roorda A; Williams DR Ophthalmology; 2006 Jun; 113(6):1019.e1. PubMed ID: 16650474 [TBL] [Abstract][Full Text] [Related]
28. Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity. Hayashi T; Gekka T; Goto-Omoto S; Takeuchi T; Kubo A; Kitahara K Ophthalmology; 2005 Dec; 112(12):2115. PubMed ID: 16225923 [TBL] [Abstract][Full Text] [Related]
29. Neuro-ophthalmic presentation of cone dysfunction syndromes in the adult. Zervas JP; Smith JL J Clin Neuroophthalmol; 1987 Dec; 7(4):202-18. PubMed ID: 2963026 [TBL] [Abstract][Full Text] [Related]
30. Progressive generalized cone dysfunction. François J; de Rouck A; Verriest G; de Laey JJ; Cambie E Ophthalmologica; 1974; 169(4):255-84. PubMed ID: 4547582 [No Abstract] [Full Text] [Related]
31. [Congenital achromatopsia]. Pinckers A Ann Ocul (Paris); 1972 Jul; 205(7):821-34. PubMed ID: 4539461 [No Abstract] [Full Text] [Related]
32. Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families. Ebenezer ND; Michaelides M; Jenkins SA; Audo I; Webster AR; Cheetham ME; Stockman A; Maher ER; Ainsworth JR; Yates JR; Bradshaw K; Holder GE; Moore AT; Hardcastle AJ Invest Ophthalmol Vis Sci; 2005 Jun; 46(6):1891-8. PubMed ID: 15914600 [TBL] [Abstract][Full Text] [Related]
33. Alström syndrome. Report of 22 cases and literature review. Russell-Eggitt IM; Clayton PT; Coffey R; Kriss A; Taylor DS; Taylor JF Ophthalmology; 1998 Jul; 105(7):1274-80. PubMed ID: 9663233 [TBL] [Abstract][Full Text] [Related]
34. [Fundus flavimaculatus and dystrophy of the cones]. Malbrel C; Foltz A; Alame M; Talmud M Bull Soc Ophtalmol Fr; 1979; 79(11-12):1099-102. PubMed ID: 317901 [No Abstract] [Full Text] [Related]
35. Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram. Renner AB; Kellner U; Cropp E; Preising MN; MacDonald IM; van den Hurk JA; Cremers FP; Foerster MH Ophthalmology; 2006 Nov; 113(11):2066.e1-10. PubMed ID: 16935340 [TBL] [Abstract][Full Text] [Related]
37. Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophy. Mäntyjärvi M; Nurmenniemi P; Partanen J; Myöhänen T; Peippo M; Alitalo T Acta Ophthalmol Scand; 2001 Aug; 79(4):359-65. PubMed ID: 11453854 [TBL] [Abstract][Full Text] [Related]
38. Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A). Jiang L; Katz BJ; Yang Z; Zhao Y; Faulkner N; Hu J; Baird J; Baehr W; Creel DJ; Zhang K Mol Vis; 2005 Feb; 11():143-51. PubMed ID: 15735604 [TBL] [Abstract][Full Text] [Related]
39. Progressive human cone-rod dysfunction (dystrophy). Fishman GA Trans Sect Ophthalmol Am Acad Ophthalmol Otolaryngol; 1976; 81(4 Pt 1):OP716-24. PubMed ID: 1085512 [TBL] [Abstract][Full Text] [Related]
40. Keratoconus associated with cone-rod dystrophy: a case report. Fogla R; Iyer GK Cornea; 2002 Apr; 21(3):331-2. PubMed ID: 11917188 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]