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.
5. Detection of mosaic retinal dysfunction in choroideremia carriers electroretinographic and psychophysical testing. Vajaranant TS; Fishman GA; Szlyk JP; Grant-Jordan P; Lindeman M; Seiple W Ophthalmology; 2008 Apr; 115(4):723-9. PubMed ID: 18201765 [TBL] [Abstract][Full Text] [Related]
6. Fluorescein angiography in potential carriers for choroideremia. An additional aid for final diagnosis, when funduscopy shows equivocal symptoms. van Dorp DB; van Balen AT Ophthalmic Paediatr Genet; 1985 Feb; 5(1-2):25-30. PubMed ID: 4058868 [TBL] [Abstract][Full Text] [Related]
7. An electroretinographic and molecular genetic study of X-linked cone degeneration. Reichel E; Bruce AM; Sandberg MA; Berson EL Am J Ophthalmol; 1989 Nov; 108(5):540-7. PubMed ID: 2554733 [TBL] [Abstract][Full Text] [Related]
8. Choroideremia. A clinical and genetic study of 84 Finnish patients and 126 female carriers. Kärnä J Acta Ophthalmol Suppl (1985); 1986; 176():1-68. PubMed ID: 3014804 [TBL] [Abstract][Full Text] [Related]
9. Local macular electroretinographic responses in idiopathic central serous chorioretinopathy. Miyake Y; Shiroyama N; Ota I; Horiguchi M Am J Ophthalmol; 1988 Nov; 106(5):546-50. PubMed ID: 3189469 [TBL] [Abstract][Full Text] [Related]
10. Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram. Renner AB; Kellner U; Cropp E; Preising MN; MacDonald IM; van den Hurk JA; Cremers FP; Foerster MH Ophthalmology; 2006 Nov; 113(11):2066.e1-10. PubMed ID: 16935340 [TBL] [Abstract][Full Text] [Related]
11. Electroretinograms in microcephaly with chorioretinal degeneration. Manning FJ; Bruce AM; Berson EL Am J Ophthalmol; 1990 Apr; 109(4):457-63. PubMed ID: 2330949 [TBL] [Abstract][Full Text] [Related]
12. Electroretinographic testing as an aid in detection of carriers of X-chromosome-linked retinitis pigmentosa. Berson EL; Rosen JB; Simonoff EA Am J Ophthalmol; 1979 Apr; 87(4):460-8. PubMed ID: 443310 [TBL] [Abstract][Full Text] [Related]
13. Full-field electroretinograms in infants with hereditary tapetoretinal degeneration. Andréasson S; Ponjavic V Acta Ophthalmol Scand Suppl; 1996; (219):19-21. PubMed ID: 8741109 [TBL] [Abstract][Full Text] [Related]
14. Foveal cone electroretinograms in retinitis pigmentosa and juvenile maular degeneration. Sandberg MA; Jacobson SG; Berson EL Am J Ophthalmol; 1979 Oct; 88(4):702-7. PubMed ID: 507142 [TBL] [Abstract][Full Text] [Related]
15. Photoreceptor dysfunction in central areolar choroidal dystrophy. Rothman RJ Ann Ophthalmol; 1994; 26(1):25-30. PubMed ID: 8198367 [TBL] [Abstract][Full Text] [Related]
16. Heredity of the choroidal dystrophies. François J Adv Ophthalmol; 1978; 35():1-25. PubMed ID: 343550 [TBL] [Abstract][Full Text] [Related]
17. Pathological study in a female carrier of choroideremia. Ghosh M; McCulloch C; Parker JA Can J Ophthalmol; 1988 Jun; 23(4):181-6. PubMed ID: 3395922 [TBL] [Abstract][Full Text] [Related]
18. The relation of rhodopsin and scotopic sensitivity in choroideremia. Fulton AB; Hansen RM Am J Ophthalmol; 1987 Nov; 104(5):524-32. PubMed ID: 3674186 [TBL] [Abstract][Full Text] [Related]
19. Differential diagnosis of diffuse choroidal atrophies. Diffuse choriocapillaris atrophy, choroideremia, and gyrate atrophy of the choroid and retina. Hayasaka S; Shoji K; Kanno C; Oura F; Mizuno K Retina; 1985; 5(1):30-7. PubMed ID: 4001587 [TBL] [Abstract][Full Text] [Related]
20. [Choroideremia: report on a pedigree (author's transl)]. Satoh M Nippon Ganka Gakkai Zasshi; 1979 Feb; 83(2):118-27. PubMed ID: 312592 [No Abstract] [Full Text] [Related] [Next] [New Search]