Literature DB >> 13180620

Electroretinography in cases of night blindness.

L A RIGGS.   

Abstract

Entities:  

Keywords:  NIGHT BLINDNESS/diagnosis; RETINA/physiology

Mesh:

Year:  1954        PMID: 13180620     DOI: 10.1016/0002-9394(54)90011-2

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


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  32 in total

1.  A study of the visual functions in patients with retinal pigmentary degeneration following the use of NP 207.

Authors:  H M BURIAN; M C FLETCHER
Journal:  Trans Am Ophthalmol Soc       Date:  1958

2.  [The electroretinogram in retinitis pigmentosa after stimulation with light of high intensity].

Authors:  W LEHNERT
Journal:  Albrecht Von Graefes Arch Ophthalmol       Date:  1963

3.  [The electroretinogram and adaptation capacity in retinitis pigmentosa-with a contribution to the theory of the extinguished ERG].

Authors:  J KUEPER; W MUELLER-LIMMROTH
Journal:  Albrecht Von Graefes Arch Ophthalmol       Date:  1960

4.  Electro-retinography in children.

Authors:  R P DHANDA
Journal:  Indian J Pediatr       Date:  1956-10       Impact factor: 1.967

5.  Electro-oculography as a functional test in pathological conditions of the fundus. I. First results.

Authors:  J FRANCOIS; G VERRIEST; A DE ROUCK
Journal:  Br J Ophthalmol       Date:  1956-02       Impact factor: 4.638

Review 6.  Rod densitometry in night blindness: a review and two puzzling cases. Rod densitometry in night blindness.

Authors:  J E Keunen; G J Van Meel; D Van Norren
Journal:  Doc Ophthalmol       Date:  1988 Mar-Apr       Impact factor: 2.379

7.  Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.

Authors:  Michael F Marmor; Christina Zeitz
Journal:  Doc Ophthalmol       Date:  2018-07-26       Impact factor: 2.379

8.  Cone function in congenital nyctalopia.

Authors:  I M Siegel; V C Greenstein; W H Seiple; R E Carr
Journal:  Doc Ophthalmol       Date:  1987-03       Impact factor: 2.379

9.  Congenital stationary nightblindness.

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

10.  Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness.

Authors:  Ajoy Vincent; Isabelle Audo; Erika Tavares; Jason T Maynes; Anupreet Tumber; Thomas Wright; Shuning Li; Christelle Michiels; Christel Condroyer; Heather MacDonald; Robert Verdet; José-Alain Sahel; Christian P Hamel; Christina Zeitz; Elise Héon
Journal:  Am J Hum Genet       Date:  2016-04-07       Impact factor: 11.025

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