Visual function and genetic analysis of families with a progressive Stargardt-like disease

被引：0
|
作者：
Sharon, D [1 ]
Beit-Ya'akov, A [1 ]
Obolensky, A [1 ]
Meissonnier-Mizrahi, L [1 ]
Bejarano-Achache, I [1 ]
Neis, R [1 ]
Blumenfeld, A [1 ]
Rosenmann, A [1 ]
Banin, E [1 ]
机构：
[1] Hebrew Univ Jerusalem, Hadassah Med Ctr, Dept Ophthalmol, IL-91010 Jerusalem, Israel
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2004年 / 45卷
关键词：
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
4721
引用
收藏
页码：U508 / U508
页数：1
相关论文
共 50 条
  • [41] A genetic analysis of familial aggregation in Inflammatory Bowel Disease multiplex families
    Jans, D.
    Lee, H. S.
    Ferrante, M.
    Vermeire, S.
    Cleynen, I.
    JOURNAL OF CROHNS & COLITIS, 2023, 17 : 1013 - 1014
  • [42] MOLECULAR GENETIC ANALYSIS IN FAMILIES WITH AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE
    Obeidova, Lena
    Stekrova, Jitka
    Elisakova, Veronika
    Seeman, Tomas
    Reiterova, Jana
    Tesar, Vladimir
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2015, 30
  • [43] Families With Wilson's Disease in Subsequent Generations: Clinical and Genetic Analysis
    Dziezyc, Karolina
    Litwin, Tomasz
    Chabik, Grzegorz
    Gramza, Karolina
    Czlonkowska, Anna
    MOVEMENT DISORDERS, 2014, 29 (14) : 1828 - 1832
  • [44] Genetic analysis of four consanguineous multiplex families with inflammatory bowel disease
    Ben-Yosef, Noam
    Frampton, Matthew
    Schiff, Elena R.
    Daher, Saleh
    Abu Baker, Fadi
    Safadi, Rifaat
    Israeli, Eran
    Segal, Anthony W.
    Levine, Adam P.
    GASTROENTEROLOGY REPORT, 2021, 9 (06): : 521 - 532
  • [45] Identification of Genetic Defects in 33 Probands with Stargardt Disease by WES-Based Bioinformatics Gene Panel Analysis
    Xin, Wei
    Xiao, Xueshan
    Li, Shiqiang
    Jia, Xiaoyun
    Guo, Xiangming
    Zhang, Qingjiong
    PLOS ONE, 2015, 10 (07):
  • [46] Identification of Novel Mutations in ABCA4 Gene: Clinical and Genetic Analysis of Indian Patients with Stargardt Disease
    Battu, Rajani
    Verma, Anshuman
    Hariharan, Ramesh
    Krishna, Shuba
    Kiran, Ravi
    Jacob, Jemima
    Ganapathy, Aparna
    Ramprasad, Vedam L.
    Kumaramanickavel, Govindasamy
    Jeyabalan, Nallathambi
    Ghosh, Arkasubhra
    BIOMED RESEARCH INTERNATIONAL, 2015, 2015
  • [47] The Visual Function Index (VF-14) reflects a notable loss in Vision-Related Quality of Life (VRQOL) in Stargardt Disease
    Zaremba, Justin Tyler
    Strecker, Zach
    DeBartolomeo, Gabrielle
    Tsang, Stephen H.
    Kay, Christine Nichols
    Connor, Thomas B.
    Gorin, Michael B.
    Bernstein, Paul S.
    Lam, Byron L.
    Washington, Ilyas
    Scholl, Hendrik P.
    Saad, Leonide
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2019, 60 (09)
  • [48] Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1)
    Gehrig, A
    Felbor, U
    Kelsell, RE
    Hunt, DM
    Maumenee, IH
    Weber, BHF
    JOURNAL OF MEDICAL GENETICS, 1998, 35 (08) : 641 - 645
  • [49] Visual function and gene analysis in a family with Oguchi's disease
    Yoshii, M
    Murakami, A
    Akeo, K
    Nakamura, A
    Shimoyama, M
    Ikeda, Y
    Kikuchi, Y
    Okisaka, S
    Yanashima, K
    Oguchi, Y
    OPHTHALMIC RESEARCH, 1998, 30 (06) : 394 - 401
  • [50] Linkage analysis of a family with dominant Stargardt's-like macular dystrophy - evidence of a novel disease locus.
    O'Connor, ST
    Sperber, D
    Yang, Z
    Yu, Z
    Zhang, H
    Li, Y
    Zhang, K
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2001, 42 (04) : S639 - S639
12345