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OGUCHI'S DISEASE.

作者信息

CARR R E, GOURAS P

出版信息

Arch Ophthalmol. 1965 May;73:646-56. doi: 10.1001/archopht.1965.00970030648010.

DOI:10.1001/archopht.1965.00970030648010

PMID:14281981

Abstract

摘要

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OGUCHI'S DISEASE.

Arch Ophthalmol. 1965 May;73:646-56. doi: 10.1001/archopht.1965.00970030648010.

PHOTOPIC FLICKER ERG IN CASES OF CONGENITAL NIGHT BLINDNESS AND TOTAL COLOR BLINDNESS.

Doc Ophthalmol. 1964;18:352-66. doi: 10.1007/BF00160587.

Some visual characteristics of Oguchi's disease.

Doc Ophthalmol. 1966;20:406-19. doi: 10.1007/BF00165431.

LEBER'S DISEASE IN THE NETHERLANDS.

Doc Ophthalmol. 1963;17:1-162. doi: 10.1007/BF00573524.

[Fluorescein fundus angiographic findings of Oguchi's disease].

Nippon Ganka Gakkai Zasshi. 1970 Mar;74(3):235-40.

[Fluorescence fundus angiography of Oguchi's disease].

Nippon Ganka Gakkai Zasshi. 1969 Mar;73(3):371-6.

ELECTROPHYSIOLOGIC ASPECTS OF SEVERAL RETINAL DISEASES.

Am J Ophthalmol. 1964 Jul;58:95-107.

[A fluorescein angiographic study of Oguchi's disease].

Nihon Ganka Kiyo. 1969 Sep;20(9):894-9.

ELECTROPHYSIOLOGICAL STUDIES IN EARLY RETINITIS PIGMENTOSA.

Arch Ophthalmol. 1964 Jul;72:104-10. doi: 10.1001/archopht.1964.00970020106022.

THE RED-LIGHT ABSOLUTE THRESHOLD IN HETEROZYGOTE PROTAN CARRIERS. POSSIBLE GENETIC IMPLICATIONS.

Invest Ophthalmol. 1964 Feb;3:107-18.

引用本文的文献

Grk1 Missense Mutations in Type II Oguchi Disease: A Literature Review.

Ann Biomed Res. 2024;5(2):1-7. doi: 10.61545/abr-5-128.

A non-stop S-antigen gene mutation is associated with late onset hereditary retinal degeneration in dogs.

Mol Vis. 2013 Aug 27;19:1871-84. eCollection 2013.

A Chinese family with Oguchi's disease due to compound heterozygosity including a novel deletion in the arrestin gene.

Mol Vis. 2012;18:528-36. Epub 2012 Mar 1.

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

Mol Vis. 2009 Sep 5;15:1788-93.

Shortening of the rod outer segment in Oguchi disease.

Graefes Arch Clin Exp Ophthalmol. 2009 Nov;247(11):1561-3. doi: 10.1007/s00417-009-1114-6. Epub 2009 Jun 11.

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.

J Neurosci. 2001 Dec 1;21(23):9175-84. doi: 10.1523/JNEUROSCI.21-23-09175.2001.

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

Proc Natl Acad Sci U S A. 1998 Mar 17;95(6):2824-7. doi: 10.1073/pnas.95.6.2824.

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

Br J Ophthalmol. 1997 Dec;81(12):1043-5. doi: 10.1136/bjo.81.12.1043.

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

Proc Natl Acad Sci U S A. 1998 Jan 6;95(1):328-33. doi: 10.1073/pnas.95.1.328.

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

J Med Genet. 1995 May;32(5):396-8. doi: 10.1136/jmg.32.5.396.

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OGUCHI'S DISEASE.

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