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Journal Abstract Search

146 related items for PubMed ID: 7362813

  • 1. Sector retinitis pigmentosa in juvenile nephronophthisis.
    Godel V, Iaina A, Nemet P, Lazar M.
    Br J Ophthalmol; 1980 Feb; 64(2):124-6. PubMed ID: 7362813
    [Abstract] [Full Text] [Related]

  • 2. Retinal manifestations in familial juvenile nephronophthisis.
    Godel V, Iaina A, Nemet P, Lazar M.
    Clin Genet; 1979 Oct; 16(4):277-81. PubMed ID: 519897
    [Abstract] [Full Text] [Related]

  • 3. Hereditary renal-retinal dysplasia.
    Godel V, Iaina A, Nemet P, Lazar M.
    Doc Ophthalmol; 1980 Oct 15; 49(2):347-59. PubMed ID: 7438990
    [Abstract] [Full Text] [Related]

  • 4. [Hereditary chorioretinal degeneration and nephronophthisis. The role of Senior-Löken syndrome].
    Orssaud C, Kleinknecht C, Habib R, Broyer M.
    Ophtalmologie; 1989 Oct 15; 3(4):270-2. PubMed ID: 2641132
    [Abstract] [Full Text] [Related]

  • 5. Retinitis pigmentosa and allied diseases: applications of electroretinographic testing.
    Berson EL.
    Int Ophthalmol; 1981 Aug 15; 4(1-2):7-22. PubMed ID: 7028651
    [Abstract] [Full Text] [Related]

  • 6. Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa.
    McLaughlin ME, Ehrhart TL, Berson EL, Dryja TP.
    Proc Natl Acad Sci U S A; 1995 Apr 11; 92(8):3249-53. PubMed ID: 7724547
    [Abstract] [Full Text] [Related]

  • 7. [Ocular manifestations associated with nephronophthisis and genetic study in three Tunisian families].
    Sellami D, Makni K, Chaker H, Kharrat M, Hentati N, Kammoun K, Chabouni F, Ben Hamida M, Hachicha J, Salomon R, Antignac C, Ayadi H, Feki J.
    J Fr Ophtalmol; 2006 Nov 11; 29(9):1019-23. PubMed ID: 17114995
    [Abstract] [Full Text] [Related]

  • 8. Hereditary renal-retinal dysplasia and the medullary cystic disease-nephronophthisis complex.
    Avasthi PS, Erickson DG, Gardner KD.
    Ann Intern Med; 1976 Feb 11; 84(2):157-61. PubMed ID: 766680
    [Abstract] [Full Text] [Related]

  • 9. 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 11; 36(11):2186-92. PubMed ID: 7558711
    [Abstract] [Full Text] [Related]

  • 10. Cystic disease of the renal medulla associated with retinitis pigmentosa and imino acid abnormalities.
    Bennett WM, Simon NM, Krill AE, Weinstein RF, Carone FA.
    Clin Nephrol; 1975 Jul 11; 4(1):25-31. PubMed ID: 1157347
    [Abstract] [Full Text] [Related]

  • 11. Familial ocular anomalies in juvenile nephronophthisis.
    Godel V, Iaina A, Goldman B.
    Metab Pediatr Ophthalmol; 1980 Jul 11; 4(1):25-9. PubMed ID: 6969336
    [No Abstract] [Full Text] [Related]

  • 12. Retinitis pigmentosa and allied retinal diseases: electrophysiologic findings.
    Berson EL.
    Trans Sect Ophthalmol Am Acad Ophthalmol Otolaryngol; 1976 Jul 11; 81(4 Pt 1):OP659-666. PubMed ID: 960388
    [Abstract] [Full Text] [Related]

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  • 14. [From gene to disease: from the ABCA4 gene to Stargardt disease, cone-rod dystrophy and retinitis pigmentosa].
    Cremers FP, Maugeri A, Klevering BJ, Hoefsloot LH, Hoyng CB.
    Ned Tijdschr Geneeskd; 2002 Aug 24; 146(34):1581-4. PubMed ID: 12224481
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  • 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 10; 528(2):178-82. PubMed ID: 23900199
    [Abstract] [Full Text] [Related]

  • 18. Childhood cone-rod dystrophy with macular cystic degeneration from recessive CRB1 mutation.
    Khan AO, Aldahmesh MA, Abu-Safieh L, Alkuraya FS.
    Ophthalmic Genet; 2014 Sep 10; 35(3):130-7. PubMed ID: 23767994
    [Abstract] [Full Text] [Related]

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  • 20. Autosomal recessive retinitis pigmentosa and Coats disease: a presumed familial incidence.
    Lanier JD, McCrary JA, Justice J.
    Arch Ophthalmol; 1976 Oct 10; 94(10):1737-42. PubMed ID: 973820
    [Abstract] [Full Text] [Related]

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