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Journal Abstract Search

184 related items for PubMed ID: 9775220

  • 21. Prenatal ultrastructural diagnosis in the neuronal ceroid-lipofuscinoses.
    Goebel HH.
    Pathol Res Pract; 1994 Aug; 190(7):728-33. PubMed ID: 7808971
    [Abstract] [Full Text] [Related]

  • 22. "Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology.
    Robson AG, Webster AR, Michaelides M, Downes SM, Cowing JA, Hunt DM, Moore AT, Holder GE.
    Retina; 2010 Jan; 30(1):51-62. PubMed ID: 19952985
    [Abstract] [Full Text] [Related]

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  • 24. Human pathology in NCL.
    Anderson GW, Goebel HH, Simonati A.
    Biochim Biophys Acta; 2013 Nov; 1832(11):1807-26. PubMed ID: 23200925
    [Abstract] [Full Text] [Related]

  • 25. Neurological deterioration in late infantile neuronal ceroid lipofuscinosis.
    Worgall S, Kekatpure MV, Heier L, Ballon D, Dyke JP, Shungu D, Mao X, Kosofsky B, Kaplitt MG, Souweidane MM, Sondhi D, Hackett NR, Hollmann C, Crystal RG.
    Neurology; 2007 Aug 07; 69(6):521-35. PubMed ID: 17679671
    [Abstract] [Full Text] [Related]

  • 26. Electroretinogram in cone dystrophy.
    Iijima H, Yamaguchi S, Kogure S, Hosaka O, Shibutani T.
    Jpn J Ophthalmol; 1991 Aug 07; 35(4):453-66. PubMed ID: 1821435
    [Abstract] [Full Text] [Related]

  • 27. Electronegative electroretinogram in mucolipidosis IV.
    Pradhan SM, Atchaneeyasakul LO, Appukuttan B, Mixon RN, McFarland TJ, Billingslea AM, Wilson DJ, Stout JT, Weleber RG.
    Arch Ophthalmol; 2002 Jan 07; 120(1):45-50. PubMed ID: 11786056
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  • 29. Cone-rod dependence in the rat retina: variation with the rate of rod damage.
    Chrysostomou V, Valter K, Stone J.
    Invest Ophthalmol Vis Sci; 2009 Jun 07; 50(6):3017-23. PubMed ID: 19182251
    [Abstract] [Full Text] [Related]

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  • 31. The effect of age on human cone and rod ganzfeld electroretinograms.
    Weleber RG.
    Invest Ophthalmol Vis Sci; 1981 Mar 07; 20(3):392-9. PubMed ID: 7203883
    [Abstract] [Full Text] [Related]

  • 32. Neuronal ceroid lipofuscinoses and possible pathogenic mechanism.
    Zhong N.
    Mol Genet Metab; 2000 Mar 07; 71(1-2):195-206. PubMed ID: 11001811
    [Abstract] [Full Text] [Related]

  • 33. Retinal function in aging homozygous Cln3 (Δex7/8) knock-in mice.
    Volz C, Mirza M, Langmann T, Jägle H.
    Adv Exp Med Biol; 2014 Mar 07; 801():495-501. PubMed ID: 24664736
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  • 36. Loci for classical and a variant late infantile neuronal ceroid lipofuscinosis map to chromosomes 11p15 and 15q21-23.
    Sharp JD, Wheeler RB, Lake BD, Savukoski M, Järvelä IE, Peltonen L, Gardiner RM, Williams RE.
    Hum Mol Genet; 1997 Apr 07; 6(4):591-5. PubMed ID: 9097964
    [Abstract] [Full Text] [Related]

  • 37. [Clinical and electroencephalographic aspects of late infantile neuronal ceroid lipofuscinosis].
    Caraballo R, Sologuestua A, Ruggieri VL, Monges S, Cersósimo R, Taratuto AL, Medina C, Fejerman N.
    Rev Neurol; 1997 Apr 07; 40(3):135-40. PubMed ID: 15750896
    [Abstract] [Full Text] [Related]

  • 38. [Multi-flash ERG in cone dystrophies and cone-rod dystrophies].
    Walter P, Widder RA, Brunner R.
    Klin Monbl Augenheilkd; 1998 Feb 07; 212(2):88-92. PubMed ID: 9577807
    [Abstract] [Full Text] [Related]

  • 39. Retinal pigment epithelial dysfunction in human immunodeficiency virus-infected patients with cytomegalovirus retinitis.
    Harrison JM, van Heuven WA.
    Ophthalmology; 1999 Apr 07; 106(4):790-7. PubMed ID: 10201604
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