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Journal Abstract Search

215 related items for PubMed ID: 9888420

  • 21. Recurrent episodes of night blindness in a patient with short bowel syndrome.
    Renner AB, Dietrich-Ntoukas T, Jägle H.
    Doc Ophthalmol; 2015 Dec; 131(3):221-30. PubMed ID: 26507840
    [Abstract] [Full Text] [Related]

  • 22. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
    Smith PR, Bain SC, Good PA, Hattersley AT, Barnett AH, Gibson JM, Dodson PM.
    Ophthalmology; 1999 Jun; 106(6):1101-8. PubMed ID: 10366077
    [Abstract] [Full Text] [Related]

  • 23. [Electroretinogram and electrooculogram in a family with Stargardt's disease].
    Pojda-Wilczek D, Makowiecka-Obidzińska K, Herba E.
    Klin Oczna; 2004 Jun; 106(3 Suppl):540-1. PubMed ID: 15636262
    [Abstract] [Full Text] [Related]

  • 24. Blue-on-yellow perimetry in the complete type of congenital stationary night blindness.
    Terasaki H, Miyake Y, Nomura R, Horiguchi M, Suzuki S, Kondo M.
    Invest Ophthalmol Vis Sci; 1999 Oct; 40(11):2761-4. PubMed ID: 10509678
    [Abstract] [Full Text] [Related]

  • 25. Hypotrichosis with juvenile macular dystrophy: clinical and electrophysiological assessment of visual function.
    Leibu R, Jermans A, Hatim G, Miller B, Sprecher E, Perlman I.
    Ophthalmology; 2006 May; 113(5):841-7.e3. PubMed ID: 16650681
    [Abstract] [Full Text] [Related]

  • 26. Abnormalities of the photoreceptor-bipolar cell synapse in a substrain of C57BL/10 mice.
    Ruether K, Grosse J, Matthiessen E, Hoffmann K, Hartmann C.
    Invest Ophthalmol Vis Sci; 2000 Nov; 41(12):4039-47. PubMed ID: 11053310
    [Abstract] [Full Text] [Related]

  • 27. Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunction.
    Michaelides M, Jenkins SA, Brantley MA, Andrews RM, Waseem N, Luong V, Gregory-Evans K, Bhattacharya SS, Fitzke FW, Webster AR.
    Invest Ophthalmol Vis Sci; 2006 Jul; 47(7):3085-97. PubMed ID: 16799055
    [Abstract] [Full Text] [Related]

  • 28. 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
    [Abstract] [Full Text] [Related]

  • 29. Rod-cone dystrophy with maculopathy in genetic glutathione synthetase deficiency: a morphologic and electrophysiologic study.
    Burstedt MS, Ristoff E, Larsson A, Wachtmeister L.
    Ophthalmology; 2009 Feb; 116(2):324-31. PubMed ID: 19111905
    [Abstract] [Full Text] [Related]

  • 30. Alström syndrome--a case report and literature review.
    Karska-Basta I, Kubicka-Trzaska A, Filemonowicz-Skoczek A, Romanowska-Dixon B, Kobylarz J.
    Klin Oczna; 2008 Feb; 110(4-6):188-92. PubMed ID: 18655459
    [Abstract] [Full Text] [Related]

  • 31. Electrophysiological findings in patients with Oguchi's disease.
    Miyake Y, Horiguchi M, Suzuki S, Kondo M, Tanikawa A.
    Jpn J Ophthalmol; 1996 Feb; 40(4):511-9. PubMed ID: 9130055
    [Abstract] [Full Text] [Related]

  • 32. Biochemical but not clinical vitamin A deficiency results from mutations in the gene for retinol binding protein.
    Biesalski HK, Frank J, Beck SC, Heinrich F, Illek B, Reifen R, Gollnick H, Seeliger MW, Wissinger B, Zrenner E.
    Am J Clin Nutr; 1999 May; 69(5):931-6. PubMed ID: 10232633
    [Abstract] [Full Text] [Related]

  • 33. The distribution of retinol-binding protein and its mRNA in the rat eye.
    Herbert J, Cavallaro T, Martone R.
    Invest Ophthalmol Vis Sci; 1991 Feb; 32(2):302-9. PubMed ID: 1993581
    [Abstract] [Full Text] [Related]

  • 34. CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.
    Aleman TS, Soumittra N, Cideciyan AV, Sumaroka AM, Ramprasad VL, Herrera W, Windsor EA, Schwartz SB, Russell RC, Roman AJ, Inglehearn CF, Kumaramanickavel G, Stone EM, Fishman GA, Jacobson SG.
    Invest Ophthalmol Vis Sci; 2009 Dec; 50(12):5944-54. PubMed ID: 19578027
    [Abstract] [Full Text] [Related]

  • 35. A detailed phenotypic study of "cone dystrophy with supernormal rod ERG".
    Michaelides M, Holder GE, Webster AR, Hunt DM, Bird AC, Fitzke FW, Mollon JD, Moore AT.
    Br J Ophthalmol; 2005 Mar; 89(3):332-9. PubMed ID: 15722315
    [Abstract] [Full Text] [Related]

  • 36. Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.
    Nishiguchi KM, Sandberg MA, Gorji N, Berson EL, Dryja TP.
    Hum Mutat; 2005 Mar; 25(3):248-58. PubMed ID: 15712225
    [Abstract] [Full Text] [Related]

  • 37. Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness.
    Nakamura M, Ito S, Terasaki H, Miyake Y.
    Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1610-6. PubMed ID: 11381068
    [Abstract] [Full Text] [Related]

  • 38. Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.
    Schatz P, Ponjavic V, Andréasson S, McGee TL, Dryja TP, Abrahamson M.
    Ophthalmic Genet; 2005 Sep; 26(3):119-24. PubMed ID: 16272056
    [Abstract] [Full Text] [Related]

  • 39. Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration.
    Lewis CA, Batlle IR, Batlle KG, Banerjee P, Cideciyan AV, Huang J, Alemán TS, Huang Y, Ott J, Gilliam TC, Knowles JA, Jacobson SG.
    Invest Ophthalmol Vis Sci; 1999 Aug; 40(9):2106-14. PubMed ID: 10440267
    [Abstract] [Full Text] [Related]

  • 40. 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; 26(3):111-7. PubMed ID: 16272055
    [Abstract] [Full Text] [Related]

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