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Results: 1-10 |
Results: 10
STARGARDTS-DISEASE AND RETINITIS-PIGMENTOSA IN THE SAME PEDIGREE
Authors: KYLE GM PEARCE IA DUVALLYOUNG J
Citation: Gm. Kyle et al., STARGARDTS-DISEASE AND RETINITIS-PIGMENTOSA IN THE SAME PEDIGREE, Vision research, 36, 1996, pp. 425-425
THE BINDING-PROPERTIES OF INDOCYANINE GREEN (ICG) SIGNIFICANCE IN ICGIMAGING
Authors: YONEYA S SAITO T KOMATSU Y DUVALLYOUNG J
Citation: S. Yoneya et al., THE BINDING-PROPERTIES OF INDOCYANINE GREEN (ICG) SIGNIFICANCE IN ICGIMAGING, Vision research, 36, 1996, pp. 2421-2421
IMMUNOCYTOCHEMICAL STUDY OF RETINAL DIODE-LASER PHOTOCOAGULATION IN THE RAT
Authors: RICHARDSON PRS BOULTON ME DUVALLYOUNG J MCLEOD D
Citation: Prs. Richardson et al., IMMUNOCYTOCHEMICAL STUDY OF RETINAL DIODE-LASER PHOTOCOAGULATION IN THE RAT, British journal of ophthalmology, 80(12), 1996, pp. 1092-1098
THE ROLE OF MOLECULAR-GENETICS IN THE PRENATAL-DIAGNOSIS OF RETINAL DYSTROPHIES
Authors: EVANS K GREGORY CY FRYER A WHITTAKER J DUVALLYOUNG J BIRD AC JAY MR BHATTACHARYA SS
Citation: K. Evans et al., THE ROLE OF MOLECULAR-GENETICS IN THE PRENATAL-DIAGNOSIS OF RETINAL DYSTROPHIES, Eye, 9, 1995, pp. 24-28
CHROMOSOME 19Q CONE-ROD RETINAL DYSTROPHY - OCULAR PHENOTYPE
Authors: EVANS K DUVALLYOUNG J FITZKE FW ARDEN GB BHATTACHARYA SS BIRD AC
Citation: K. Evans et al., CHROMOSOME 19Q CONE-ROD RETINAL DYSTROPHY - OCULAR PHENOTYPE, Archives of ophthalmology, 113(2), 1995, pp. 195-201
GENETIC-LINKAGE OF CONE-ROD RETINAL DYSTROPHY TO CHROMOSOME 19Q AND EVIDENCE FOR SEGREGATION DISTORTION
Authors: EVANS K FRYER A INGLEHEARN C DUVALLYOUNG J WHITTAKER JL GREGORY CY BUTLER R EBENEZER N HUNT DM BHATTACHARYA S
Citation: K. Evans et al., GENETIC-LINKAGE OF CONE-ROD RETINAL DYSTROPHY TO CHROMOSOME 19Q AND EVIDENCE FOR SEGREGATION DISTORTION, Nature genetics, 6(2), 1994, pp. 210-213
TRAUMATIC RETINAL ANGIOPATHY AND SEAT BELTS - PATHOGENESIS OF WHIPLASH INJURY
Authors: HASLETT RS DUVALLYOUNG J MCGALLIARD JN
Citation: Rs. Haslett et al., TRAUMATIC RETINAL ANGIOPATHY AND SEAT BELTS - PATHOGENESIS OF WHIPLASH INJURY, Eye, 8, 1994, pp. 615-617
FUNCTIONAL VISUAL DEFICIT IN CHILDREN WITH A FAMILY HISTORY OF RETINITIS-PIGMENTOSA
Authors: HOLDEN R DUVALLYOUNG J
Citation: R. Holden et J. Duvallyoung, FUNCTIONAL VISUAL DEFICIT IN CHILDREN WITH A FAMILY HISTORY OF RETINITIS-PIGMENTOSA, Journal of pediatric ophthalmology and strabismus, 31(5), 1994, pp. 323-324
GENETIC LOCALIZATION OF CONE-ROD RETINAL DYSTROPHY TO CHROMOSOME-19Q
Authors: EVANS K FRYER A INGLEHEARN C DUVALLYOUNG J WHITTAKER J GREGORY CY HUNT D BHATTACHARYA S
Citation: K. Evans et al., GENETIC LOCALIZATION OF CONE-ROD RETINAL DYSTROPHY TO CHROMOSOME-19Q, Investigative ophthalmology & visual science, 35(4), 1994, pp. 1313-1313
ELECTROPHYSIOLOGY OF TYPE-II MESANGIOCAPILLARY GLOMERULONEPHRITIS WITH ASSOCIATED FUNDUS ABNORMALITIES
Authors: OBRIEN C DUVALLYOUNG J BROWN M SHORT C BONE M
Citation: C. Obrien et al., ELECTROPHYSIOLOGY OF TYPE-II MESANGIOCAPILLARY GLOMERULONEPHRITIS WITH ASSOCIATED FUNDUS ABNORMALITIES, British journal of ophthalmology, 77(12), 1993, pp. 778-780
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