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.
91 related articles for article (PubMed ID: 5156821)
1. Clinical and electrophysiological observations on genetic carriers of retinis pigmentosa in a family (pedigree Tt) showing intermediate sex-linked inheritance. Imaizumi K; Takahashi R; Tazawa Y; Yamada K; Mita K Vision Res; 1971 Oct; 11(10):1215-6. PubMed ID: 5156821 [No Abstract] [Full Text] [Related]
2. Clinical and electrophysiological observations on genetic carriers of retinitis pigmentosa in a family (pedigree Tt) showing sex-linked inheritance. Imaizumi K; Takahashi R; Tazawa Y; Yamada K; Mita K Adv Exp Med Biol; 1972; 24(0):301-7. PubMed ID: 4671885 [No Abstract] [Full Text] [Related]
3. Clinical measures of visual function in familial retinitis pigmentosa. Williams TD; Lovasik JV Am J Optom Physiol Opt; 1985 Jan; 62(1):45-51. PubMed ID: 3976835 [TBL] [Abstract][Full Text] [Related]
4. Clinical symptoms at different ages in autosomal dominant retinitis pigmentosa. A family study in three generations. Mäntyjärvi M; Tuppurainen K Ophthalmologica; 1994; 208(1):23-8. PubMed ID: 8145980 [TBL] [Abstract][Full Text] [Related]
5. The clinical significance of retinitis pigmentosa without pigment: a computer assisted analysis. Pearlman JT; Saxton J; Flood TP; Seiff SR Adv Exp Med Biol; 1977; 77():31-5. PubMed ID: 322461 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Visual Function in Carriers of X-Linked Retinitis Pigmentosa. Comander J; Weigel-DiFranco C; Sandberg MA; Berson EL Ophthalmology; 2015 Sep; 122(9):1899-906. PubMed ID: 26143542 [TBL] [Abstract][Full Text] [Related]
9. A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa. Grover S; Fishman GA; Anderson RJ; Lindeman M Ophthalmology; 2000 Feb; 107(2):386-96. PubMed ID: 10690843 [TBL] [Abstract][Full Text] [Related]
10. Electrophysiological and psychophysical findings in Hunter syndrome. Abraham FA; Yatziv S; Russell A; Auerbach E Arch Ophthalmol; 1974 Mar; 91(3):181-6. PubMed ID: 4205505 [No Abstract] [Full Text] [Related]
11. Temporal aspects of the electroretinogram in sector retinitis pigmentosa. Berson EL; Howard J Arch Ophthalmol; 1971 Dec; 86(6):653-65. PubMed ID: 5128159 [No Abstract] [Full Text] [Related]
12. Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutation. Rosenfeld PJ; Hahn LB; Sandberg MA; Dryja TP; Berson EL Invest Ophthalmol Vis Sci; 1995 Oct; 36(11):2186-92. PubMed ID: 7558711 [TBL] [Abstract][Full Text] [Related]
13. Sector retinitis pigmentosa. Krill AE; Archer D; Martin D Am J Ophthalmol; 1970 Jun; 69(6):977-87. PubMed ID: 5423778 [No Abstract] [Full Text] [Related]
14. The functional syndromes. François J Ophthalmologica; 1974; 169(1-3):234-9. PubMed ID: 4547324 [No Abstract] [Full Text] [Related]
15. The relation of rhodopsin and scotopic retinal sensitivity in sector retinitis pigmentosa. Fulton AB; Hansen RM Am J Ophthalmol; 1988 Feb; 105(2):132-40. PubMed ID: 3341429 [TBL] [Abstract][Full Text] [Related]
16. Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene. Andréasson S; Ponjavic V; Abrahamson M; Ehinger B; Wu W; Fujita R; Buraczynska M; Swaroop A Am J Ophthalmol; 1997 Jul; 124(1):95-102. PubMed ID: 9222238 [TBL] [Abstract][Full Text] [Related]
17. Cosegregation of X-linked retinitis pigmentosa and hemophilia A. Rabinowitz YS; Ladda RL; Sassani JW; Eyster ME Am J Ophthalmol; 1988 Jan; 105(1):46-56. PubMed ID: 3337193 [TBL] [Abstract][Full Text] [Related]