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kw.\*:("Degeneración coriorretiniana hereditaria Stargardt")

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Stargardt's disease: the evolution of a diagnosisSMITH, B. F; SMITH, J. B; LOW, J et al.Journal of pediatric ophthalmology and strabismus. 1987, Vol 24, Num 5, pp 259-262, issn 0191-3913Article

Unilateral macular oedema in Zermatt and Stargardt macular dystrophiesABOUZEID, H; WOLFENSBERGER, T. J; SCHORDERET, D. F et al.British journal of ophthalmology. 2009, Vol 93, Num 10, issn 0007-1161, 1376-1377, 1407-1408 [4 p.]Article

Clinical and Genetic Characteristics of Late-onset Stargardt's DiseaseHAAFTEN, Sarah C. Westeneng-Van; BOON, Camiel J. F; CREMERS, Frans P. M et al.Ophthalmology (Rochester, MN). 2012, Vol 119, Num 6, pp 1199-1210, issn 0161-6420, 12 p.Article

A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophyMAUGERI, Alessandra; MEIRE, Francoise; HOYNG, Carel B et al.Investigative ophthalmology & visual science. 2004, Vol 45, Num 12, pp 4263-4267, issn 0146-0404, 5 p.Article

Angiomatose rétinienne associée à une maladie de Stargardt. A propos d'un cas clinique = Retinal angiomatosis in association with Stargardt's disease: one case reportRETSAS, C; SARKS, J; SHANAHAN, L et al.Journal français d'ophtalmologie. 1989, Vol 12, Num 12, pp 857-862, issn 0181-5512, 6 p.Conference Paper

L'hérédité dans la maladie de Stargardt et le fundus flavimaculatus = Heredity in stargardt disease and fundus flavimaculatusTURUT, P; PUECH, B.Ophtalmologie. 1989, Vol 3, Num 3, pp 187-192Conference Paper

Dominant inheritance of Stargardt's diseaseBITHER, P. P; BERNS, L. A.Journal of the American Optometric Association. 1988, Vol 59, Num 2, pp 112-117, issn 0003-0244Article

Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosaKLEVERING, B. Jeroen; MAUGERI, Alessandra; WANNER, Anja et al.Ophthalmology (Rochester, MN). 2004, Vol 111, Num 3, pp 546-553, issn 0161-6420, 8 p.Article

L- and M-cone-driven electroretinograms in Stargardt's macular dystrophy-fundus flavimaculatusSCHOLL, Hendrik P. N; KREMERS, Jan; VONTHEIN, Reinhard et al.Investigative ophthalmology & visual science. 2001, Vol 42, Num 6, pp 1380-1389, issn 0146-0404Article

Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR (ABCA4)YATSENKO, Alexander N; SHROYER, Noah F; LEWIS, Richard Alan et al.Human genetics. 2001, Vol 108, Num 4, pp 346-355, issn 0340-6717Article

Complex inheritance of ABCR mutations in Stargardt disease : linkage disequilibrium, complex alleles, and pseudodominanceSHROYER, N. F; LEWIS, R. A; LUPSKI, J. R et al.Human genetics. 2000, Vol 106, Num 2, pp 244-248, issn 0340-6717Article

Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundus flavimaculatusLOIS, N; HOLDER, G. E; FITZKE, F. W et al.Investigative ophthalmology & visual science. 1999, Vol 40, Num 11, pp 2668-2675, issn 0146-0404Article

Recent advances in the genetics of macular dystrophiesMAH, D. Y; WONG, P. W; EDWARDS, A et al.Canadian journal of ophthalmology. 1998, Vol 33, Num 3, pp 135-143, issn 0008-4182Article

Initial rapid decrease in visual acuity in siblings with Stargardt's diseaseHAYASAKA, S; KUROME, H; NODA, S et al.Japanese journal of ophthalmology. 1993, Vol 37, Num 4, pp 485-489, issn 0021-5155Article

training the bioptic telescope wearer for drivingVOGEL, G. L.Journal of the American Optometric Association. 1991, Vol 62, Num 4, pp 288-293, issn 0003-0244, 6 p.Article

Mode évolutif du Fundus Flavimaculatus avec Stargardt = Evolutionary mode of Fundus Flavimaculatus and Stargardt's diseaseBALE, F; HOCHART, G; PUECH, B et al.Bulletin des sociétés d'ophtalmologie de France. 1989, Vol 89, Num 2, pp 283-287, issn 0081-1270Article

Dystrophie héréditaire juvénile de la macula chez une famille nombreuse d'Epire = Juvenile hereditary dystrophy of the macula (Stargardt's disease)KITSOS, G; COTE, G. B; KALOGERO-POULOS, C et al.Journal français d'ophtalmologie. 1989, Vol 12, Num 10, pp 669-671, issn 0181-5512, 3 p.Conference Paper

Eccentric Fixation in Stargardt's Disease Assessed by Tübingen PerimetryMESSIAS, Andre; REINHARD, Jens; AUGUSTO VELASCO E CRUZ, Antonio et al.Investigative ophthalmology & visual science. 2007, Vol 48, Num 12, pp 5815-5822, issn 0146-0404, 8 p.Article

Colour recognition at large visual eccentricities in normal observers and patients with low visionNAÏLI, Fatima; DESPRETZ, Pascal; BOUCART, Muriel et al.Neuroreport (Oxford). 2006, Vol 17, Num 15, pp 1571-1574, issn 0959-4965, 4 p.Article

Fundus autofluorescence in Stargardt macular dystrophy-fundus flavimaculatusLOIS, Noemi; HALFYARD, Anthony S; BIRD, Alan C et al.American journal of ophthalmology. 2004, Vol 138, Num 1, pp 55-63, issn 0002-9394, 9 p.Article

Lipofuscin and macular degenerationWOLF, George.Nutrition reviews. 2003, Vol 61, Num 10, pp 342-346, issn 0029-6643, 5 p.Article

ABCA4 gene mutations in Japanese patients with Stargardt disease and retinitis pigmentosaFUKUI, Takehiro; YAMAMOTO, Shuji; OKADA, Annabelle A et al.Investigative ophthalmology & visual science. 2002, Vol 43, Num 9, pp 2819-2824, issn 0146-0404Article

Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatusLOIS, Noemi; HOLDER, Graham E; BUNCE, Catey et al.Archives of ophthalmology (1960). 2001, Vol 119, Num 3, pp 359-369, issn 0003-9950Article

A novel gene for autosomal dominant stargardt-like macular dystrophy with homology to the SUR4 protein familyEDWARDS, Albert O; DONOSO, Larry A; RITTER, Robert III et al.Investigative ophthalmology & visual science. 2001, Vol 42, Num 11, pp 2652-2663, issn 0146-0404Article

A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt diseaseKANG ZHANG; GARIBALDI, D. C; KNIAZEVA, M et al.American journal of ophthalmology. 1999, Vol 128, Num 6, pp 720-724, issn 0002-9394Article

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