These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
113 related items for PubMed ID: 18767495
1. [The ocular features in a father and a son with central areolar choroidal dystrophy]. Okuno T, Oku H, Sugasawa J, Hamamura HW, Nakamura K, Ikeda T. Nippon Ganka Gakkai Zasshi; 2008 Aug; 112(8):688-94. PubMed ID: 18767495 [Abstract] [Full Text] [Related]
2. The development of central areolar choroidal dystrophy. Hoyng CB, Deutman AF. Graefes Arch Clin Exp Ophthalmol; 1996 Feb; 234(2):87-93. PubMed ID: 8720677 [Abstract] [Full Text] [Related]
3. Sveinsson chorioretinal atrophy: the mildest changes are located in the photoreceptor outer segment/retinal pigment epithelium junction. Jonasson F, Sander B, Eysteinsson T, Jörgensen T, Klintworth GK. Acta Ophthalmol Scand; 2007 Dec; 85(8):862-7. PubMed ID: 17683515 [Abstract] [Full Text] [Related]
4. Clinical features and linkage analysis for a Chinese family with autosomal dominant central areolar choroidal dystrophy. Ma K, Yang XF, Han C, Zhang N, Xu J, Liu SB, Lu H, Snellingen T, Wang NL, Liu NP. Chin Med J (Engl); 2009 Nov 20; 122(22):2686-90. PubMed ID: 19951596 [Abstract] [Full Text] [Related]
5. Electrophysiology findings in a large family with central areolar choroidal dystrophy. Lotery AJ, Silvestri G, Collins AD. Doc Ophthalmol; 2009 Nov 20; 97(2):103-19. PubMed ID: 10765965 [Abstract] [Full Text] [Related]
6. [Electroretinogram and electrooculogram in a family with Stargardt's disease]. Pojda-Wilczek D, Makowiecka-Obidzińska K, Herba E. Klin Oczna; 2004 Nov 20; 106(3 Suppl):540-1. PubMed ID: 15636262 [Abstract] [Full Text] [Related]
7. Segregation of ophthalmoscopic characteristics according to choroidal thickness in patients with early age-related macular degeneration. Switzer DW, Mendonça LS, Saito M, Zweifel SA, Spaide RF. Retina; 2012 Jul 20; 32(7):1265-71. PubMed ID: 22222760 [Abstract] [Full Text] [Related]
8. Best vitelliform macular dystrophy in a Swedish family: genetic analysis and a seven-year follow-up of photodynamic treatment of a young boy with choroidal neovascularization. Frennesson CI, Wadelius C, Nilsson SE. Acta Ophthalmol; 2014 May 20; 92(3):238-42. PubMed ID: 23617333 [Abstract] [Full Text] [Related]
9. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy. Tyni T, Kivelä T, Lappi M, Summanen P, Nikoskelainen E, Pihko H. Ophthalmology; 1998 May 20; 105(5):810-24. PubMed ID: 9593380 [Abstract] [Full Text] [Related]
10. Morphologic photoreceptor abnormality in occult macular dystrophy on spectral-domain optical coherence tomography. Park SJ, Woo SJ, Park KH, Hwang JM, Chung H. Invest Ophthalmol Vis Sci; 2010 Jul 20; 51(7):3673-9. PubMed ID: 20164460 [Abstract] [Full Text] [Related]
11. Photoreceptor dysfunction in central areolar choroidal dystrophy. Rothman RJ. Ann Ophthalmol; 1994 Jul 20; 26(1):25-30. PubMed ID: 8198367 [Abstract] [Full Text] [Related]
15. Optical coherence tomography of chorioretinal and choroidal folds. Giuffrè G, Distefano MG. Acta Ophthalmol Scand; 2007 May 20; 85(3):333-6. PubMed ID: 17488465 [Abstract] [Full Text] [Related]
16. Common spectral domain OCT and electrophysiological findings in different pattern dystrophies. Hannan SR, de Salvo G, Stinghe A, Shawkat F, Lotery AJ. Br J Ophthalmol; 2013 May 20; 97(5):605-10. PubMed ID: 23426737 [Abstract] [Full Text] [Related]
18. Full-field electroretinograms in patients with central areolar choroidal dystrophy. Ponjavic V, Andréasson S, Ehinger B. Acta Ophthalmol (Copenh); 1994 Oct 20; 72(5):537-44. PubMed ID: 7887150 [Abstract] [Full Text] [Related]
19. [A new approach for studying the retinal and choroidal circulation]. Yoneya S. Nippon Ganka Gakkai Zasshi; 2004 Dec 20; 108(12):836-61; discussion 862. PubMed ID: 15656089 [Abstract] [Full Text] [Related]
20. Autosomal dominant vitreoretinochoroidopathy with normal electrooculogram in a German family. Kellner U, Jandeck C, Kraus H, Foerster MH. Graefes Arch Clin Exp Ophthalmol; 1998 Feb 20; 236(2):109-14. PubMed ID: 9498121 [Abstract] [Full Text] [Related] Page: [Next] [New Search]