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Journal Abstract Search
117 related items for PubMed ID: 30267901
21. [Oguchi disease or stationary congenital night blindness: a case report]. Boissonnot M, Robert MF, Gilbert-Dussardier B, Dighiero P. J Fr Ophtalmol; 2007 Jan; 30(1):e2. PubMed ID: 17287664 [Abstract] [Full Text] [Related]
22. Congenital stationary night blindness associated with morning glory disc malformation: a novel hemizygous mutation in CACNA1F. Abdelkader E, AlHilali S, Neuhaus C, Bergmann C, AlMurshed T, Schatz P. Ophthalmic Genet; 2018 Oct; 39(5):659-661. PubMed ID: 30067413 [No Abstract] [Full Text] [Related]
23. A Chinese family with Oguchi's disease due to compound heterozygosity including a novel deletion in the arrestin gene. Huang L, Li W, Tang W, Zhu X, Ou-Yang P, Lu G. Mol Vis; 2012 Oct; 18():528-36. PubMed ID: 22419846 [Abstract] [Full Text] [Related]
27. Oguchi disease: phenotypic characteristics of patients with the frequent 1147delA mutation in the arrestin gene. Nakazawa M, Wada Y, Fuchs S, Gal A, Tamai M. Retina; 1997 Oct; 17(1):17-22. PubMed ID: 9051837 [Abstract] [Full Text] [Related]
28. Novel mutations in the GRK1 gene in Japanese patients With Oguchi disease. Oishi A, Akimoto M, Kawagoe N, Mandai M, Takahashi M, Yoshimura N. Am J Ophthalmol; 2007 Sep; 144(3):475-7. PubMed ID: 17765441 [Abstract] [Full Text] [Related]
31. Gene analysis and evaluation of the single founder effect in Japanese patients with Oguchi disease. Saga M, Mashima Y, Kudoh J, Oguchi Y, Shimizu N. Jpn J Ophthalmol; 2004 Sep; 48(4):350-2. PubMed ID: 15295660 [Abstract] [Full Text] [Related]
32. Clinical characterisation of the CABP4-related retinal phenotype. Khan AO, Alrashed M, Alkuraya FS. Br J Ophthalmol; 2013 Mar; 97(3):262-5. PubMed ID: 23099293 [Abstract] [Full Text] [Related]
37. Oguchi's disease: two cases and literature review. Dai Y, Sun T. J Int Med Res; 2021 May; 49(5):3000605211019921. PubMed ID: 34057838 [Abstract] [Full Text] [Related]
38. A novel GRK1 mutation in an Italian patient with Oguchi disease. Mucciolo DP, Sodi A, Murro V, Passerini I, Palchetti S, Pelo E, Virgili G, Rizzo S. Ophthalmic Genet; 2018 May; 39(1):137-138. PubMed ID: 28511019 [No Abstract] [Full Text] [Related]
40. [A case of Oguchi disease with disappearance of golden tapetal-like fundus reflex after vitreous resection]. Kuroda M, Hirami Y, Nishida A, Jin ZB, Ishigami C, Takahashi M, Kurimoto Y. Nippon Ganka Gakkai Zasshi; 2011 Oct; 115(10):916-23. PubMed ID: 22117325 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]