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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

109 related articles for article (PubMed ID: 3966999)

  • 1. Studies on retinitis pigmentosa in man. II. Erythrocyte osmotic fragility.
    Hussain AA; Voaden MJ
    Br J Ophthalmol; 1985 Feb; 69(2):126-8. PubMed ID: 3966999
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Studies on retinitis pigmentosa in man. I. Taurine and blood platelets.
    Voaden MJ; Hussain AA; Chan IP
    Br J Ophthalmol; 1982 Dec; 66(12):771-5. PubMed ID: 7171527
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: retinal histopathology and immunocytochemistry.
    Li ZY; Jacobson SG; Milam AH
    Exp Eye Res; 1994 Apr; 58(4):397-408. PubMed ID: 7925677
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Concentric retinitis pigmentosa: clinicopathologic correlations.
    Milam AH; De Castro EB; Smith JE; Tang WX; John SK; Gorin MB; Stone EM; Aguirre GD; Jacobson SG
    Exp Eye Res; 2001 Oct; 73(4):493-508. PubMed ID: 11825021
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.
    Jacobson SG; Buraczynska M; Milam AH; Chen C; Järvaläinen M; Fujita R; Wu W; Huang Y; Cideciyan AV; Swaroop A
    Invest Ophthalmol Vis Sci; 1997 Sep; 38(10):1983-97. PubMed ID: 9331262
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and serum lipid findings in a large family with autosomal dominant retinitis pigmentosa.
    Newsome DA; Anderson RE; May JG; McKay TA; Maude M
    Ophthalmology; 1988 Dec; 95(12):1691-5. PubMed ID: 3266001
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Possible role of altered levels of plasma docosahexaenoic acid in the pathogenesis of retinitis pigmentosa. Preliminary results].
    Simonelli F; Milone A; Iura A; Picardi C; La Banca AM; Cotticelli L; Rinaldi E
    Boll Soc Ital Biol Sper; 1990 Sep; 66(9):893-8. PubMed ID: 2149985
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa.
    Sullivan LS; Heckenlively JR; Bowne SJ; Zuo J; Hide WA; Gal A; Denton M; Inglehearn CF; Blanton SH; Daiger SP
    Nat Genet; 1999 Jul; 22(3):255-9. PubMed ID: 10391212
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa.
    Ayuso C; Garcia-Sandoval B; Najera C; Valverde D; Carballo M; Antiñolo G
    Clin Genet; 1995 Sep; 48(3):120-2. PubMed ID: 8556816
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa.
    Rosenfeld PJ; Cowley GS; McGee TL; Sandberg MA; Berson EL; Dryja TP
    Nat Genet; 1992 Jun; 1(3):209-13. PubMed ID: 1303237
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Studies on blood from patients with dominantly-inherited retinitis pigmentosa.
    Voaden MJ; Polkinghorne PJ; Belin J; Smith AD
    Prog Clin Biol Res; 1989; 314():57-68. PubMed ID: 2608680
    [No Abstract]   [Full Text] [Related]  

  • 13. Retinitis pigmentosa in South Africa.
    Oswald AH; Goldblatt J; Sampson G; Clokie R; Beighton P
    S Afr Med J; 1985 Dec; 68(12):863-6. PubMed ID: 4071341
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ultrastructure of connecting cilia in different forms of retinitis pigmentosa.
    Barrong SD; Chaitin MH; Fliesler SJ; Possin DE; Jacobson SG; Milam AH
    Arch Ophthalmol; 1992 May; 110(5):706-10. PubMed ID: 1580851
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosa.
    Martinez-Gimeno M; Maseras M; Baiget M; Beneito M; Antiñolo G; Ayuso C; Carballo M
    Hum Mutat; 2001 Jun; 17(6):520. PubMed ID: 11385710
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Retinitis pigmentosa and bilateral cystoid macular oedema in a patient heterozygous for the RIM1 mutation previously associated with cone-rod dystrophy 7.
    Warwick AN; Shawkat F; Lotery AJ
    Ophthalmic Genet; 2017; 38(2):178-182. PubMed ID: 27176872
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exome sequencing identifies RDH12 compound heterozygous mutations in a family with severe retinitis pigmentosa.
    Chacon-Camacho OF; Jitskii S; Buentello-Volante B; Quevedo-Martinez J; Zenteno JC
    Gene; 2013 Oct; 528(2):178-82. PubMed ID: 23900199
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evaluation of fatty acids in membrane phospholipids of erythrocytes in retinitis pigmentosa patients.
    Simonelli F; Manna C; Romano N; Nunziata G; Voto O; Rinaldi E
    Ophthalmic Res; 1996; 28(2):93-8. PubMed ID: 8792359
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Discordance for retinitis pigmentosa in two monozygotic twin pairs.
    Berghmans LV; de Mendonça RH; Coppieters F; de Oliveira Maia O; Takahashi WY; Lissens W; de Baere E; Leroy BP
    Retina; 2011 Jun; 31(6):1164-9. PubMed ID: 21283054
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic rescue models refute nonautonomous rod cell death in retinitis pigmentosa.
    Koch SF; Duong JK; Hsu CW; Tsai YT; Lin CS; Wahl-Schott CA; Tsang SH
    Proc Natl Acad Sci U S A; 2017 May; 114(20):5259-5264. PubMed ID: 28468800
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.