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Journal Abstract Search

94 related items for PubMed ID: 3369131

  • 21. Newborn screening for Krabbe disease: the New York State model.
    Duffner PK, Caggana M, Orsini JJ, Wenger DA, Patterson MC, Crosley CJ, Kurtzberg J, Arnold GL, Escolar ML, Adams DJ, Andriola MR, Aron AM, Ciafaloni E, Djukic A, Erbe RW, Galvin-Parton P, Helton LE, Kolodny EH, Kosofsky BE, Kronn DF, Kwon JM, Levy PA, Miller-Horn J, Naidich TP, Pellegrino JE, Provenzale JM, Rothman SJ, Wasserstein MP.
    Pediatr Neurol; 2009 Apr; 40(4):245-52; discussion 253-5. PubMed ID: 19302934
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  • 22. Differentiation of rare leukodystrophies by post-mortem morphological and biochemical studies: female adrenoleukodystrophy-like disease and late-onset Krabbe disease.
    Gullotta F, Hughes JL, Wittkowski W, Poulos A, Sträter R, Bernheimer H, Harzer K.
    Neuropediatrics; 1996 Feb; 27(1):37-41. PubMed ID: 8677024
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  • 23. Application of a galactosylceramidase microassay method to early prenatal diagnosis of Krabbe's disease.
    Tsutsumi O, Satoh K, Sakamoto S, Suzuki Y, Kato T.
    Clin Chim Acta; 1982 Nov 10; 125(3):265-73. PubMed ID: 7172437
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  • 33. [Comparison of spectrophotometric and fluorimetric methods of determination of galactocerebroside-beta-D-galactosidase in leukocytes].
    Gusina NB, Tsukerman GL.
    Vopr Med Khim; 1988 Nov 10; 34(4):129-31. PubMed ID: 3195126
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  • 34. Characterization of the rhesus monkey galactocerebrosidase (GALC) cDNA and gene and identification of the mutation causing globoid cell leukodystrophy (Krabbe disease) in this primate.
    Luzi P, Rafi MA, Victoria T, Baskin GB, Wenger DA.
    Genomics; 1997 Jun 01; 42(2):319-24. PubMed ID: 9192853
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  • 36. Pathogenesis of leukodystrophy for Krabbe disease: molecular mechanism and clinical treatment.
    Sakai N.
    Brain Dev; 2009 Aug 01; 31(7):485-7. PubMed ID: 19332366
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