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Journal Abstract Search

526 related items for PubMed ID: 15162299

  • 21. Fundus autofluorescence imaging in Best's vitelliform dystrophy.
    Jarc-Vidmar M, Kraut A, Hawlina M.
    Klin Monbl Augenheilkd; 2003 Dec; 220(12):861-7. PubMed ID: 14704944
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  • 22. A 30-year follow-up of a neuronal ceroid lipofuscinosis patient with mutations in CLN3 and protracted disease course.
    Aberg L, Lauronen L, Hämäläinen J, Mole SE, Autti T.
    Pediatr Neurol; 2009 Feb; 40(2):134-7. PubMed ID: 19135632
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  • 23. Altered gene expression in the eye of a mouse model for batten disease.
    Chattopadhyay S, Kingsley E, Serour A, Curran TM, Brooks AI, Pearce DA.
    Invest Ophthalmol Vis Sci; 2004 Sep; 45(9):2893-905. PubMed ID: 15326100
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  • 24. Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration.
    Ku CA, Hull S, Arno G, Vincent A, Carss K, Kayton R, Weeks D, Anderson GW, Geraets R, Parker C, Pearce DA, Michaelides M, MacLaren RE, Robson AG, Holder GE, Heon E, Raymond FL, Moore AT, Webster AR, Pennesi ME.
    JAMA Ophthalmol; 2017 Jul 01; 135(7):749-760. PubMed ID: 28542676
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  • 27. Electroretinographic and clinicopathologic correlations of retinal dysfunction in infantile neuronal ceroid lipofuscinosis (infantile Batten disease).
    Weleber RG, Gupta N, Trzupek KM, Wepner MS, Kurz DE, Milam AH.
    Mol Genet Metab; 2004 Jul 01; 83(1-2):128-37. PubMed ID: 15464427
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  • 30. Developmental impairments of select neurotransmitter systems in brains of Cln3(Deltaex7/8) knock-in mice, an animal model of juvenile neuronal ceroid lipofuscinosis.
    Herrmann P, Druckrey-Fiskaaen C, Kouznetsova E, Heinitz K, Bigl M, Cotman SL, Schliebs R.
    J Neurosci Res; 2008 Jun 01; 86(8):1857-70. PubMed ID: 18265413
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  • 31. Phenotypic variation in enhanced S-cone syndrome.
    Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE.
    Invest Ophthalmol Vis Sci; 2008 May 01; 49(5):2082-93. PubMed ID: 18436841
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  • 32. Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
    Wissinger B, Dangel S, Jägle H, Hansen L, Baumann B, Rudolph G, Wolf C, Bonin M, Koeppen K, Ladewig T, Kohl S, Zrenner E, Rosenberg T.
    Invest Ophthalmol Vis Sci; 2008 Feb 01; 49(2):751-7. PubMed ID: 18235024
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  • 33. Further Characterization of the Predominant Inner Retinal Degeneration of Aging Cln3 Δex7/8 Knock-In Mice.
    Volz C, Mirza M, Langmann T, Jägle H.
    Adv Exp Med Biol; 2018 Feb 01; 1074():403-411. PubMed ID: 29721970
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  • 35. A mouse gene knockout model for juvenile ceroid-lipofuscinosis (Batten disease).
    Katz ML, Shibuya H, Liu PC, Kaur S, Gao CL, Johnson GS.
    J Neurosci Res; 1999 Aug 15; 57(4):551-6. PubMed ID: 10440905
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  • 40. Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosis.
    Chang B, Bronson RT, Hawes NL, Roderick TH, Peng C, Hageman GS, Heckenlively JR.
    Invest Ophthalmol Vis Sci; 1994 Mar 15; 35(3):1071-6. PubMed ID: 8125718
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