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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

188 related items for PubMed ID: 15275696

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  • 25. [Prenatal diagnosis of mannosidosis using chorion villi].
    Petushkova NA, Tsvetkova IV, Fuks MA, Doronin GL, Iakubovich DV.
    Vopr Med Khim; 1987; 33(4):99-101. PubMed ID: 2958965
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  • 26. Diagnosis and prevention of lysosomal storage diseases in Russia.
    Krasnopolskaya KD, Mirenburg TV, Aronovich EL, Lebedeva TV, Odinokova ON, Demina NA, Kozlova VM, Kuznetsov MI.
    J Inherit Metab Dis; 1993; 16(6):994-1002. PubMed ID: 8127076
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  • 27. Juvenile GM1 gangliosidosis. Occurrence with absence of two beta-galactosidase components.
    Lowden JA, Callahan JW, Norman MG, Thain M, Prichard JS.
    Arch Neurol; 1974 Sep; 31(3):200-3. PubMed ID: 4368854
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  • 33. [Study of the specificity of human lysosomal glycolipid hydrolases using synthetic fluorogenic substrates].
    Vidershaĭn GIa, Kozlova IK, Il'ina GS, Mikhaĭlova MA.
    Bioorg Khim; 1988 Aug; 14(8):1014-26. PubMed ID: 3146253
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  • 34. Molecular genetics of metachromatic leukodystrophy.
    Gieselmann V, Polten A, Kreysing J, Kappler J, Fluharty A, von Figura K.
    Dev Neurosci; 1991 Aug; 13(4-5):222-7. PubMed ID: 1687778
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  • 38. Heritable catabolic and anabolic disorders of lipid metabolism.
    Brady RO.
    Metabolism; 1977 Mar; 26(3):329-45. PubMed ID: 13262
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  • 39. Leukodystrophy incidence in Germany.
    Heim P, Claussen M, Hoffmann B, Conzelmann E, Gärtner J, Harzer K, Hunneman DH, Köhler W, Kurlemann G, Kohlschütter A.
    Am J Med Genet; 1997 Sep 05; 71(4):475-8. PubMed ID: 9286459
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