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Journal Abstract Search

175 related items for PubMed ID: 5668537

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  • 4. An improved method for the determination of leukocyte arylsulfatase A and its application to the diagnosis of metachromatic leukodystrophy in homozygous and heterozygous states.
    Potter JL, Timmons GD, Rinehart L, Witmer EJ.
    Clin Chim Acta; 1972 Jul; 39(2):518-23. PubMed ID: 5043787
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  • 6. Infantile metachromatic leukodystrophy. Confirmation of a prenatal diagnosis.
    Leroy JG, Van Elsen AF, Martin JJ, Dumon JE, Hulet AE, Okada S, Navarro C.
    N Engl J Med; 1973 Jun 28; 288(26):1365-9. PubMed ID: 4707419
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  • 7. Studies on cerebral lipidosis. Enzymatic diagnosis of metachromatic leukodystrophy.
    Yabuuchi H, Sumi K.
    Acta Paediatr Jpn; 1970 Dec 28; 12(2):1-3. PubMed ID: 4993715
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  • 9. Late adult metachromatic leukodystrophy. Arylsulfatase A activity of leukocytes in two families.
    Pilz H.
    Arch Neurol; 1972 Jul 28; 27(1):87-90. PubMed ID: 5049684
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  • 10. The use of white cells as a source of diagnostic material for lipid storage diseases.
    Snyder RA, Brady RO.
    Clin Chim Acta; 1969 Aug 28; 25(2):331-8. PubMed ID: 4895581
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  • 11. Metachromatic leukodystrophy: ambiguity of heterozygote identification.
    Kihara H, Porter MT, Fluharty AL, Scott ML, De la Flor SD, Trammell JL, Nakamura RN.
    Am J Ment Defic; 1973 Jan 28; 77(4):389-94. PubMed ID: 4706397
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  • 12. [Familial metachromatic leucodystrophy--arylsulfatase A activity of leukocytes and probable carrier state].
    Nanba K, Taniguchi N.
    Nihon Shonika Gakkai Zasshi; 1970 Jun 28; 74(6):590-5. PubMed ID: 5465441
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  • 13. Metachromatic leukodystrophy. Treatment with arylsulfatase-A.
    Greene HL, Hug G, Schubert WK.
    Arch Neurol; 1969 Feb 28; 20(2):147-53. PubMed ID: 5818425
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  • 14. Studies on arylsulfatase-A activity in metachromatic leucodystrophy.
    Komiya K, Arima M.
    Paediatr Univ Tokyo; 1970 Dec 28; 18():99-104. PubMed ID: 5535257
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  • 15. Inheritance of the enzyme deficiency in three neurolipidoses: variant 0 of Tay-Sachs disease (Sandhoff's disease), classic Tay-Sachs disease, and metachromatic leukodystrophy. Identification of the heterozygous carriers.
    Harzer K.
    Humangenetik; 1973 Dec 28; 20(1):9-24. PubMed ID: 4776531
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  • 16. [Enzymatic diagnosis of glycolipidosis].
    Zambotti V, Di Donato S, Rimoldi M, Tettamanti G.
    Quad Sclavo Diagn; 1972 Mar 28; 8(1):183-98. PubMed ID: 4351703
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  • 17. Infantile and adult-onset metachromatic leukodystrophy. Biochemical comparisons and predictive diagnosis.
    Percy AK, Kaback MM.
    N Engl J Med; 1971 Sep 30; 285(14):785-7. PubMed ID: 5567265
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  • 18. Diagnostic techniques in metachromatic leukodystrophy.
    Julius R, Buehler B, Aylsworth A, Petery LS, Rennert O, Greer M.
    Neurology; 1971 Jan 30; 21(1):15-8. PubMed ID: 4099955
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  • 19. Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophy.
    Rattazzi MC, Marks JS, Davidson RG.
    Am J Hum Genet; 1973 May 30; 25(3):310-6. PubMed ID: 4704863
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  • 20. The biochemical differentiation between heterozygote carriers of metachromatic leucodystrophy and normal persons.
    Gabreëls F, Lamers K, Kok J, Loonen M, Lommen E.
    Neuropadiatrie; 1971 Apr 30; 2(4):461-9. PubMed ID: 5171491
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