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139 related items for PubMed ID: 11738458
1. Analysis of photoreceptor function and inner retinal activity in juvenile X-linked retinoschisis. Khan NW, Jamison JA, Kemp JA, Sieving PA. Vision Res; 2001 Dec; 41(28):3931-42. PubMed ID: 11738458 [Abstract] [Full Text] [Related]
2. On- and off-responses of the photopic electroretinograms in X-linked juvenile retinoschisis. Shinoda K, Ohde H, Mashima Y, Inoue R, Ishida S, Inoue M, Kawashima S, Oguchi Y. Am J Ophthalmol; 2001 Apr; 131(4):489-94. PubMed ID: 11292413 [Abstract] [Full Text] [Related]
3. On-response deficit in the electroretinogram of the cone system in X-linked retinoschisis. Alexander KR, Fishman GA, Barnes CS, Grover S. Invest Ophthalmol Vis Sci; 2001 Feb; 42(2):453-9. PubMed ID: 11157882 [Abstract] [Full Text] [Related]
4. Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene. Eksandh LC, Ponjavic V, Ayyagari R, Bingham EL, Hiriyanna KT, Andréasson S, Ehinger B, Sieving PA. Arch Ophthalmol; 2000 Aug; 118(8):1098-104. PubMed ID: 10922205 [Abstract] [Full Text] [Related]
5. Retinal Function in X-Linked Juvenile Retinoschisis. Ambrosio L, Hansen RM, Kimia R, Fulton AB. Invest Ophthalmol Vis Sci; 2019 Nov 01; 60(14):4872-4881. PubMed ID: 31747688 [Abstract] [Full Text] [Related]
6. High-frequency attenuation of the cone ERG and ON-response deficits in X-linked retinoschisis. Alexander KR, Barnes CS, Fishman GA. Invest Ophthalmol Vis Sci; 2001 Aug 01; 42(9):2094-101. PubMed ID: 11481277 [Abstract] [Full Text] [Related]
7. Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave. Sieving PA, Bingham EL, Kemp J, Richards J, Hiriyanna K. Am J Ophthalmol; 1999 Aug 01; 128(2):179-84. PubMed ID: 10458173 [Abstract] [Full Text] [Related]
8. Temporal frequency deficits in the electroretinogram of the cone system in X-linked retinoschisis. Alexander KR, Fishman GA, Grover S. Vision Res; 2000 Aug 01; 40(20):2861-8. PubMed ID: 10960656 [Abstract] [Full Text] [Related]
9. Clinical and electroretinographic findings of female carriers and affected males in a progressive X-linked cone-rod dystrophy (COD-1) pedigree. Brown J, Kimura AE, Gorin MB. Ophthalmology; 2000 Jun 01; 107(6):1104-10. PubMed ID: 10857830 [Abstract] [Full Text] [Related]
10. Mutations of the XLRS1 gene cause abnormalities of photoreceptor as well as inner retinal responses of the ERG. Bradshaw K, George N, Moore A, Trump D. Doc Ophthalmol; 1999 Jun 01; 98(2):153-73. PubMed ID: 10947001 [Abstract] [Full Text] [Related]
12. Clinical characteristics of 14 japanese patients with X-linked juvenile retinoschisis associated with XLRS1 mutation. Shinoda K, Ishida S, Oguchi Y, Mashima Y. Ophthalmic Genet; 2000 Sep 01; 21(3):171-80. PubMed ID: 11035549 [Abstract] [Full Text] [Related]
13. Electroretinographic findings in three family members with X-linked juvenile retinoschisis associated with a novel Pro192Thr mutation of the XLRS1 gene. Tanimoto N, Usui T, Takagi M, Hasegawa S, Abe H, Sekiya K, Miyagawa Y, Nakazawa M. Jpn J Ophthalmol; 2002 Sep 01; 46(5):568-76. PubMed ID: 12457918 [Abstract] [Full Text] [Related]
14. Juvenile X-linked retinoschisis with normal scotopic b-wave in the electroretinogram at an early stage of the disease. Eksandh L, Andréasson S, Abrahamson M. Ophthalmic Genet; 2005 Sep 01; 26(3):111-7. PubMed ID: 16272055 [Abstract] [Full Text] [Related]
15. Abnormal 8-Hz flicker electroretinograms in carriers of X-linked retinoschisis. McAnany JJ, Park JC, Collison FT, Fishman GA, Stone EM. Doc Ophthalmol; 2016 Aug 01; 133(1):61-70. PubMed ID: 27369766 [Abstract] [Full Text] [Related]
16. Differentiation of murine models of "negative ERG" by single and repetitive light stimuli. Tanimoto N, Akula JD, Fulton AB, Weber BH, Seeliger MW. Doc Ophthalmol; 2016 Apr 01; 132(2):101-9. PubMed ID: 26996188 [Abstract] [Full Text] [Related]
17. A phenotype-genotype correlation study of X-linked retinoschisis. Vincent A, Robson AG, Neveu MM, Wright GA, Moore AT, Webster AR, Holder GE. Ophthalmology; 2013 Jul 01; 120(7):1454-64. PubMed ID: 23453514 [Abstract] [Full Text] [Related]
18. X-linked retinoschisis: RS1 mutation severity and age affect the ERG phenotype in a cohort of 68 affected male subjects. Bowles K, Cukras C, Turriff A, Sergeev Y, Vitale S, Bush RA, Sieving PA. Invest Ophthalmol Vis Sci; 2011 Nov 29; 52(12):9250-6. PubMed ID: 22039241 [Abstract] [Full Text] [Related]
19. Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutations. Caruso RC, Aleman TS, Cideciyan AV, Roman AJ, Sumaroka A, Mullins CL, Boye SL, Hauswirth WW, Jacobson SG. Invest Ophthalmol Vis Sci; 2010 Oct 29; 51(10):5304-13. PubMed ID: 20484585 [Abstract] [Full Text] [Related]
20. Post-photoreceptoral activity dominates primate photopic 32-Hz ERG for sine-, square-, and pulsed stimuli. Kondo M, Sieving PA. Invest Ophthalmol Vis Sci; 2002 Jul 29; 43(7):2500-7. PubMed ID: 12091456 [Abstract] [Full Text] [Related] Page: [Next] [New Search]