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Results: 1-18 |
Results: 18

Authors: Nishimura, DY Searby, CC Carmi, R Elbedour, K Van Maldergem, L Fulton, AB Lam, BL Powell, BR Swiderski, RE Bugge, KE Haider, NB Kwitek-Black, AE Ying, LH Duhl, DM Gorman, SW Heon, E Iannaccone, A Bonneau, D Biesecker, LG Jacobson, SG Stone, EM Sheffield, VC
Citation: Dy. Nishimura et al., Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2), HUM MOL GEN, 10(8), 2001, pp. 865-874

Authors: Afshari, MA Afshari, NA Fulton, AB
Citation: Ma. Afshari et al., Cortical visual impairment in infants and children, INT OPHTH C, 41(1), 2001, pp. 159-169

Authors: Fulton, AB Hansen, RM Petersen, RA Vanderveen, DK
Citation: Ab. Fulton et al., The rod photoreceptors in retinopathy of prematurity - An electroretinographic study, ARCH OPHTH, 119(4), 2001, pp. 499-505

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

Authors: Mayer, DL Hansen, RM Moore, BD Kim, S Fulton, AB
Citation: Dl. Mayer et al., Cycloplegic refractions in healthy children aged 1 through 48 months, ARCH OPHTH, 119(11), 2001, pp. 1625-1628

Authors: Fulton, AB Hansen, RM
Citation: Ab. Fulton et Rm. Hansen, The development of scotopic sensitivity, INV OPHTH V, 41(6), 2000, pp. 1588-1596

Authors: Hansen, RM Fulton, AB
Citation: Rm. Hansen et Ab. Fulton, Rod-mediated increment threshold functions in infants, INV OPHTH V, 41(13), 2000, pp. 4347-4352

Authors: Hansen, RM Fulton, AB
Citation: Rm. Hansen et Ab. Fulton, Background adaptation in children with a history of mild retinopathy of prematurity, INV OPHTH V, 41(1), 2000, pp. 320-324

Authors: Morris, EJ Evason, K Wiand, C L'Ecuyer, TJ Fulton, AB
Citation: Ej. Morris et al., Misdirected vimentin messenger RNA alters cell morphology and motility, J CELL SCI, 113(13), 2000, pp. 2433-2443

Authors: L'Ecuyer, TJ Schutte, BC Mendel, KA Morris, E Fulton, AB
Citation: Tj. L'Ecuyer et al., Muscle-specific transcription factors in fibroblasts expressing the alpha-striated tropomyosin 3 ' untranslated region, MOL GEN MET, 67(3), 1999, pp. 213-226

Authors: Fulton, AB
Citation: Ab. Fulton, The elastic filament system in myogenesis, REV PHYS B, 138, 1999, pp. 139-161

Authors: Timmers, AM Fox, DA He, LH Hansen, RM Fulton, AB
Citation: Am. Timmers et al., Rod photoreceptor maturation does not vary with retinal eccentricity in mammalian retina, CURR EYE R, 18(6), 1999, pp. 393-402

Authors: Fulton, AB Dodge, J Hansen, RM Williams, TP
Citation: Ab. Fulton et al., The rhodopsin content of human eyes, INV OPHTH V, 40(8), 1999, pp. 1878-1883

Authors: Hansen, RM Fulton, AB
Citation: Rm. Hansen et Ab. Fulton, The course of maturation of rod-mediated visual thresholds in infants, INV OPHTH V, 40(8), 1999, pp. 1883-1886

Authors: Fulton, AB Reynaud, X Hansen, RM Lemere, CA Parker, C Williams, TP
Citation: Ab. Fulton et al., Rod photoreceptors in infant rats with a history of oxygen exposure, INV OPHTH V, 40(1), 1999, pp. 168-174

Authors: Jiang, CG Hansen, RM Gee, BE Kurth, SS Fulton, AB
Citation: Cg. Jiang et al., Rod and rod mediated function in patients with beta-thalassemia major, DOC OPHTHAL, 96(4), 1999, pp. 333-345

Authors: Fulton, AB
Citation: Ab. Fulton, Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome) (vol 117, pg 251, 1999), ARCH OPHTH, 117(8), 1999, pp. 1099-1099

Authors: Fulton, AB
Citation: Ab. Fulton, Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome), ARCH OPHTH, 117(2), 1999, pp. 251-252
Risultati: 1-18 |