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Results: 1-8 |
Results: 8
An analysis of allelic variation in the ABCA4 gene
Authors: Webster, AR Heon, E Lotery, AJ Vandenburgh, K Casavant, TL Oh, KT Beck, G Fishman, GA Lam, BL Levin, A Heckenlively, JR Jacobson, SG Weleber, RG Sheffield, VC Stone, EM
Citation: Ar. Webster et al., An analysis of allelic variation in the ABCA4 gene, INV OPHTH V, 42(6), 2001, pp. 1179-1189
Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degeneration
Authors: Guymer, RH Heon, E Lotery, AJ Munier, FL Schorderet, DF Baird, PN McNeil, RJ Haines, H Sheffield, VC Stone, EM
Citation: Rh. Guymer et al., Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degeneration, ARCH OPHTH, 119(5), 2001, pp. 745-751
Mutations in the CRB1 gene cause Leber congenital amaurosis
Authors: Lotery, AJ Jacobson, SG Fishman, GA Weleber, RG Fulton, AB Namperumalsamy, P Heon, E Levin, AV Grover, S Rosenow, JR Kopp, KK Sheffield, VC Stone, EM
Citation: Aj. Lotery et al., Mutations in the CRB1 gene cause Leber congenital amaurosis, ARCH OPHTH, 119(3), 2001, pp. 415-420
Allelic variation in the VMD2 gene in best disease and age-related maculardegeneration
Authors: Lotery, AJ Munier, FL Fishman, GA Weleber, RG Jacobson, SG Affatigato, LM Nichols, BE Schorderet, DF Sheffield, VC Stone, EM
Citation: Aj. Lotery et al., Allelic variation in the VMD2 gene in best disease and age-related maculardegeneration, INV OPHTH V, 41(6), 2000, pp. 1291-1296
Mutation analysis of 3 genes in patients with leber congenital amaurosis
Authors: Lotery, AJ Namperumalsamy, P Jacobson, SG Weleber, RG Fishman, GA Musarella, MA Hoyt, CS Heon, E Levin, A Jan, J Lam, B Carr, RE Franklin, A Radha, S Andorf, JL Sheffield, VC Stone, EM
Citation: Aj. Lotery et al., Mutation analysis of 3 genes in patients with leber congenital amaurosis, ARCH OPHTH, 118(4), 2000, pp. 538-543
Correctable visual impairment in stroke rehabilitation patients
Authors: Lotery, AJ Wiggam, MI Jackson, AO Silvestri, G Refson, K Fullerton, KJ Gilmore, DH Beringer, TRO
Citation: Aj. Lotery et al., Correctable visual impairment in stroke rehabilitation patients, AGE AGEING, 29(3), 2000, pp. 221-222
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy
Authors: Stone, EM Lotery, AJ Munier, FL Heon, E Piguet, B Guymer, RH Vandenburgh, K Cousin, P Nishimura, D Swiderski, RE Silvestri, G Mackey, DA Hageman, GS Bird, AC Sheffield, VC Schorderet, DF
Citation: Em. Stone et al., A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy, NAT GENET, 22(2), 1999, pp. 199-202
Electrophysiology findings in a large family with central areolar choroidal dystrophy
Authors: Lotery, AJ Silvestri, G Collins, AD
Citation: Aj. Lotery et al., Electrophysiology findings in a large family with central areolar choroidal dystrophy, DOC OPHTHAL, 97(2), 1999, pp. 103-119
Risultati: 1-8 |