Literature DB >> 14281981

OGUCHI'S DISEASE.

R E CARR, P GOURAS.   

Abstract

Keywords:  ADAPTATION, OCULAR; ADOLESCENCE; COLOR PERCEPTION TESTS; COMPUTERS; ELECTROPHYSIOLOGY; FUNDUS OCULI; GENETICS, HUMAN; NYCTALOPIA; PSYCHOPHYSIOLOGY; VISUAL FIELDS

Mesh：

Year:  1965        PMID： 14281981     DOI： 10.1001/archopht.1965.00970030648010

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN： 0003-9950


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  12 in total

1.  Shortening of the rod outer segment in Oguchi disease.

Authors:  Hideaki Hashimoto; Shoji Kishi
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2009-06-11       Impact factor: 3.117

2.  Normal S cone electroretinogram b-wave in Oguchi's disease.

Authors:  S Yamamoto; M Hayashi; S Takeuchi; Y Shirao; K Kita; K Kawasaki
Journal:  Br J Ophthalmol       Date:  1997-12       Impact factor: 4.638

3.  Species-specific differences in expression of G-protein-coupled receptor kinase (GRK) 7 and GRK1 in mammalian cone photoreceptor cells: implications for cone cell phototransduction.

Authors:  E R Weiss; M H Ducceschi; T J Horner; A Li; C M Craft; S Osawa
Journal:  J Neurosci       Date:  2001-12-01       Impact factor: 6.167

4.  Congenital stationary nightblindness.

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

5.  Some visual characteristics of Oguchi's disease.

Authors:  J ten Doesschate; M Alpern; G B Lee; F Heyner
Journal:  Doc Ophthalmol       Date:  1966       Impact factor: 2.379

6.  Oguchi disease: suggestion of linkage to markers on chromosome 2q.

Authors:  M A Maw; S John; S Jablonka; B Müller; G Kumaramanickavel; R Oehlmann; M J Denton; A Gal
Journal:  J Med Genet       Date:  1995-05       Impact factor: 6.318

7.  Biochemical evidence for pathogenicity of rhodopsin kinase mutations correlated with the oguchi form of congenital stationary night blindness.

Authors:  S C Khani; L Nielsen; T M Vogt
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-17       Impact factor: 11.205

8.  Selective abnormality of the cone B-wave in a patient with retinal degeneration.

Authors:  R Young; J Price; N Gorham; M Cowart
Journal:  Doc Ophthalmol       Date:  1985-08-30       Impact factor: 2.379

9.  A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.

Authors:  Maleeha Azam; Rob W J Collin; Muhammad Imran Khan; Syed Tahir Abbas Shah; Nadeem Qureshi; Muhammad Ajmal; Anneke I den Hollander; Raheel Qamar; Frans P M Cremers
Journal:  Mol Vis       Date:  2009-09-05       Impact factor: 2.367

10.  Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man.

Authors:  A V Cideciyan; X Zhao; L Nielsen; S C Khani; S G Jacobson; K Palczewski
Journal:  Proc Natl Acad Sci U S A       Date:  1998-01-06       Impact factor: 11.205
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