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Journal Abstract Search

137 related items for PubMed ID: 3738902

  • 1. Abnormal excretion of autofluorescent lipids in urine from patients with neuronal ceroid lipofuscinosis.
    Ohashi T, Kanamoto Y, Yamaguchi S, Eto Y, Maekawa K.
    Tohoku J Exp Med; 1986 Apr; 148(4):335-9. PubMed ID: 3738902
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  • 2. Normal dolichol concentration in urine sediments from four patients with neuronal ceroid lipofuscinosis (Batten's disease).
    Paton BC, Poulos A.
    J Inherit Metab Dis; 1987 Apr; 10(1):28-32. PubMed ID: 3106713
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  • 3. Dolichols in brain and urinary sediment in neuronal ceroid lipofuscinosis.
    Wolfe LS, Ng Ying Kin NM, Palo J, Haltia M.
    Neurology; 1983 Jan; 33(1):103-6. PubMed ID: 6681549
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  • 4. Ceroid lipofuscinosis in sheep. I. Bis(monoacylglycero)phosphate, dolichol, ubiquinone, phospholipids, fatty acids, and fluorescence in liver lipopigment lipids.
    Palmer DN, Husbands DR, Winter PJ, Blunt JW, Jolly RD.
    J Biol Chem; 1986 Feb 05; 261(4):1766-72. PubMed ID: 3944107
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  • 5. Urinary sediment dolichols in the diagnosis of neuronal ceroid-lipofuscinosis.
    Wolfe LS, Palo J, Santavuori P, Andermann F, Andermann E, Jacob JC, Kolodny E.
    Ann Neurol; 1986 Mar 05; 19(3):270-4. PubMed ID: 3963771
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  • 6. Characterization of disease-specific brain fluorophores in ceroid-lipofuscinosis.
    Katz ML, Eldred GE, Siakotos AN, Koppang N.
    Am J Med Genet Suppl; 1988 Mar 05; 5():253-64. PubMed ID: 3146323
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  • 7. Urinary sediment dolichol excretion in patients with Batten disease and other neurodegenerative and storage disorders.
    Bennett MJ, Mathers NJ, Hemming FW, Zweije-Hofman I, Hosking GP.
    Pediatr Res; 1985 Feb 05; 19(2):213-6. PubMed ID: 3920636
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  • 8. Dolichyl-pyrophosphoryloligosaccharide protein oligosaccharide transferase in neuronal ceroid-lipofuscinosis.
    Van Dessel G, Lagrou A, Hilderson H, Dierick W.
    Biochem Cell Biol; 1992 Jun 05; 70(6):515-8. PubMed ID: 1449718
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  • 9. The neuronal ceroid-lipofuscinoses.
    Goebel HH.
    J Child Neurol; 1995 Nov 05; 10(6):424-37. PubMed ID: 8576551
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  • 11. Elevated urinary dolichol excretion in the Hermansky-Pudlak syndrome. Indicator of lysosomal dysfunction.
    Witkop CJ, Wolfe LS, Cal SX, White JG, Townsend D, Keenan KM.
    Am J Med; 1987 Mar 05; 82(3):463-70. PubMed ID: 3493691
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  • 12. Low molecular weight urinary peptides in ceroid-lipofuscinoses: potential biochemical markers for the juvenile subtype.
    LaBadie GU, Pullarkat RK.
    Am J Med Genet; 1990 Dec 05; 37(4):592-9. PubMed ID: 1701959
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  • 13. A rare homozygous MFSD8 single-base-pair deletion and frameshift in the whole genome sequence of a Chinese Crested dog with neuronal ceroid lipofuscinosis.
    Guo J, O'Brien DP, Mhlanga-Mutangadura T, Olby NJ, Taylor JF, Schnabel RD, Katz ML, Johnson GS.
    BMC Vet Res; 2015 Jan 03; 10():960. PubMed ID: 25551667
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  • 14. Ceroid lipofuscinosis in the border collie dog: retinal lesions in an animal model of juvenile Batten disease.
    Taylor RM, Farrow BR.
    Am J Med Genet; 1992 Feb 15; 42(4):622-7. PubMed ID: 1319117
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