Literature DB >> 13388255

[Visual function in essential hemeralopia in the Nougaret family].

A DE ROUCK, C DEJEAN, J FRANCOIS, G VERRIEST.   

Abstract

Entities:  

Keywords:  DAY BLINDNESS/heredity; VISION

Mesh：

Year:  1956        PMID： 13388255     DOI： 10.1159/000302932

Source DB:  PubMed          Journal:  Ophthalmologica        ISSN： 0030-3755            Impact factor:   3.250


× No keyword cloud information.
  4 in total

1.  Congenital stationary nightblindness.

Authors:  R E Carr
Journal:  Trans Am Ophthalmol Soc       Date:  1974

2.  Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy.

Authors:  Takaaki Hayashi; Katsuhiro Hosono; Kentaro Kurata; Satoshi Katagiri; Kei Mizobuchi; Shinji Ueno; Mineo Kondo; Tadashi Nakano; Yoshihiro Hotta
Journal:  Doc Ophthalmol       Date:  2019-10-03       Impact factor: 2.379

3.  Night blindness with depolarizing pattern of ON/OFF response in electroretinogram: a case report.

Authors:  Tomoaki Usui; Naoyuki Tanimoto; Satoshi Ueki; Atsushi Miki; Mineo Takagi; Shigeru Hasegawa; Haruki Abe
Journal:  Doc Ophthalmol       Date:  2006-02-25       Impact factor: 2.379

4.  Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance.

Authors:  S A Kabanarou; G E Holder; F W Fitzke; A C Bird; A R Webster
Journal:  Br J Ophthalmol       Date:  2004-08       Impact factor: 4.638
  4 in total

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