AN ELECTRORETINOGRAPHIC AND MOLECULAR GENETIC-STUDY OF X-LINKED CONE DEGENERATION

被引：82
|
作者：
REICHEL, E
BRUCE, AM
SANDBERG, MA
BERSON, EL
机构：
来源：
AMERICAN JOURNAL OF OPHTHALMOLOGY | 1989年 / 108卷 / 05期
关键词：
D O I：
10.1016/0002-9394(89)90431-5
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
引用
收藏
页码：540 / 547
页数：8
相关论文
共 50 条
  • [21] ELECTRORETINOGRAPHIC MEASURES IN CARRIERS OF X-LINKED RECESSIVE RETINITIS-PIGMENTOSA
    RISPOLI, E
    VINGOLO, EM
    IANNACCONE, A
    FORTE, R
    GRAMMATICO, B
    DEBERNARDO, C
    STEINDL, K
    PANNARALE, MR
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1994, 35 (04) : 2159 - 2159
  • [22] X-LINKED CONE DYSTROPHY - AN OVERLOOKED DIAGNOSIS
    PINCKERS, A
    DEUTMAN, AF
    INTERNATIONAL OPHTHALMOLOGY, 1987, 10 (04) : 241 - 243
  • [23] X-linked congenital ataxia: A clinical and genetic study
    Bertini, E
    des Portes, V
    Zanni, G
    Santorelli, F
    Dionisi-Vici, C
    Vicari, S
    Fariello, G
    Chelly, J
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2000, 92 (01): : 53 - 56
  • [24] LOCALIZATION BY LINKAGE ANALYSIS OF AN X-LINKED PROGRESSIVE CONE DEGENERATION TO XP11 REGION
    HONG, HK
    FERRELL, RE
    PAUL, TO
    GORIN, MB
    AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 138 - 138
  • [25] LIMB-GIRDLE SYNDROME - A GENETIC-STUDY OF 22 LARGE BRAZILIAN FAMILIES - COMPARISON WITH X-LINKED DUCHENNE AND BECKER DYSTROPHIES
    PASSOSBUENO, MR
    VAINZOF, M
    PAVANELLO, RDM
    PAVANELLOFILHO, I
    LIMA, MABO
    ZATZ, M
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1991, 103 (01) : 65 - 75
  • [26] Residual Cone Structure in Patients With X-Linked Cone Opsin Mutations
    Patterson, Emily J.
    Kalitzeos, Angelos
    Kasilian, Melissa
    Gardner, Jessica C.
    Neitz, Jay
    Hardcastle, Alison J.
    Neitz, Maureen
    Carroll, Joseph
    Michaelides, Michel
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2018, 59 (10) : 4238 - 4248
  • [27] Assessing cone mosaic disruption in patients with X-linked cone dysfunction
    Patterson, Emily J.
    Tee, James
    Neitz, Jay
    Langlo, Christopher S.
    Dubra, Alfredo
    Neitz, Maureen
    Dubis, Adam M.
    Hardcastle, Alison J.
    Michaelides, Michel
    Carroll, Joseph
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2015, 56 (07)
  • [28] X-LINKED LYMPHOPROLIFERATIVE DISEASE (XLP) - MOLECULAR-GENETIC STUDIES
    SCHUSTER, V
    GRIMM, T
    KRESS, W
    SEIDENSPINNER, S
    BELOHRADSKY, BH
    MULLER, P
    KRETH, HW
    KLINISCHE PADIATRIE, 1995, 207 (05): : 271 - 276
  • [29] Molecular genetic cause of X-linked retinitis pigmentosa in a Czech family
    Liskova, Petra
    Colclough, Tracy
    Hart-Holden, Niki
    Chakarova, Christina F.
    O'Grady, Anna
    Kondrova, Lucie
    Skalicka, Pavlina
    Diblik, Pavel
    Hardcastle, Alison J.
    ACTA OPHTHALMOLOGICA, 2011, 89 (02) : E213 - E215
  • [30] Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmus
    Zhao, Hui
    Huang, Xiu-Feng
    Zheng, Zhi-Li
    Deng, Wen-Li
    Lei, Xin-Lan
    Xing, Dong-Jun
    Ye, Liang
    Xu, Su-Zhong
    Chen, Jie
    Zhang, Fang
    Yu, Xin-Ping
    Jin, Zi-Bing
    BMJ OPEN, 2016, 6 (04):
12345