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Journal Abstract Search


169 related items for PubMed ID: 5062266

  • 1. Metachromatic leukodystrophy in the adult. A biochemical study.
    Hirose G, Bass NH.
    Neurology; 1972 Mar; 22(3):312-20. PubMed ID: 5062266
    [No Abstract] [Full Text] [Related]

  • 2. [Sulfatide lipoidosis in childhood].
    Hagberg B.
    Monatsschr Kinderheilkd (1902); 1967 Apr; 115(4):250-4. PubMed ID: 5592530
    [No Abstract] [Full Text] [Related]

  • 3. Late adult metachromatic leukodystrophy. Arylsulfatase A activity of leukocytes in two families.
    Pilz H.
    Arch Neurol; 1972 Jul; 27(1):87-90. PubMed ID: 5049684
    [No Abstract] [Full Text] [Related]

  • 4. 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
    [No Abstract] [Full Text] [Related]

  • 5. A pedigree study of metachromatic leukodystrophy. Biochemical identification of the carrier state.
    Bass NH, Witmer EJ, Dreifuss FE.
    Neurology; 1970 Jan 30; 20(1):52-62. PubMed ID: 5460770
    [No Abstract] [Full Text] [Related]

  • 6. Metachromatic form of diffuse cerebral sclerosis. V. The nature and significance of low sulfatase activity: a controlled study of brain, liver and kidney in four patients with metachromatic leukodystrophy (MLD).
    Austin J, Armstrong D, Shearer L.
    Arch Neurol; 1965 Dec 30; 13(6):593-614. PubMed ID: 4954756
    [No Abstract] [Full Text] [Related]

  • 7. A sporadic case of presumed Pelizaeus-Merzbacher disease.
    Liaño H, Ricoy JR, Díaz-Flores L, Gimeno A.
    Eur Neurol; 1974 Dec 30; 11(5):304-16. PubMed ID: 4850312
    [No Abstract] [Full Text] [Related]

  • 8. Deficiency of arylsulfatase A in juvenile metachromatic leucodystrophy: fibroblast studies.
    Leroy JG, Van Elsen A, Dumon JE, Radermecker J.
    Monogr Hum Genet; 1972 Dec 30; 6():148-9. PubMed ID: 4663890
    [No Abstract] [Full Text] [Related]

  • 9. Metachromatic leukodystrophy (MLD). 8. MLD in adults; diagnosis and pathogenesis.
    Austin J, Armstrong D, Fouch S, Mitchell C, Stumpf D, Shearer L, Briner O.
    Arch Neurol; 1968 Mar 30; 18(3):225-40. PubMed ID: 5642751
    [No Abstract] [Full Text] [Related]

  • 10. Studies on adult metachromatic leukodystrophy. 2. Biochemical aspects of adult cases of metachromatic leukodystrophy.
    Pilz H, Müller D.
    J Neurol Sci; 1969 Mar 30; 9(3):585-95. PubMed ID: 5367045
    [No Abstract] [Full Text] [Related]

  • 11. [Amaurotic idiocy connected with metachromatic leukodystrophy: transitional form or combination? Electron microscopic and histochemical finding].
    Bischoff A, Ulrich J.
    Acta Neuropathol; 1967 May 05; 8(3):292-308. PubMed ID: 6032928
    [No Abstract] [Full Text] [Related]

  • 12. Experimental Wallerian degeneration in peripheral nerves of dogs with globoid cell leukodystrophy.
    Fletcher TF, Kurtz HJ, Stadlan EM.
    J Neuropathol Exp Neurol; 1971 Oct 05; 30(4):593-602. PubMed ID: 5135014
    [No Abstract] [Full Text] [Related]

  • 13. Correction of abnormal cerebroside sulfate metabolism in cultured metachromatic leukodystrophy fibroblasts.
    Porter MT, Fluharty AL, Kihara H.
    Science; 1971 Jun 18; 172(3989):1263-5. PubMed ID: 5576165
    [Abstract] [Full Text] [Related]

  • 14. [Ultrastructural study of the sural nerve in metachromatic leukodystrophy].
    Ota M, Iwayama T.
    No To Shinkei; 1970 May 01; 22(5):557-67. PubMed ID: 5467630
    [No Abstract] [Full Text] [Related]

  • 15. Arylsulfatase A activity in human urine: quantitative studies on patients with lysosomal disorders including metachromatic leukodystrophy.
    Thomas GH, Howell RR.
    Clin Chim Acta; 1972 Jan 01; 36(1):99-103. PubMed ID: 5007723
    [No Abstract] [Full Text] [Related]

  • 16. Chronic sclerosing panencephalitis. I. A histological and lipid-histochemical study.
    Haltia M, Sourander P, Svennerholm L.
    Acta Neuropathol; 1970 Jan 01; 14(4):284-92. PubMed ID: 5412438
    [No Abstract] [Full Text] [Related]

  • 17. Biochemical evaluation of a combined sulfatidosis and gangliosidosis (glycolipidosis) of the brain.
    Pilz H, Jatzkewitz H.
    Pathol Eur; 1968 Jan 01; 3(2):409-15. PubMed ID: 5688473
    [No Abstract] [Full Text] [Related]

  • 18. A preclinical case of late adult metachromatic leukodystrophy? Manifestation only with lipid abnormalities in urine, enzyme deficiency and decrease of nerve conduction velocity.
    Pilz H, Hopf HC.
    J Neurol Neurosurg Psychiatry; 1972 Jun 01; 35(3):360-4. PubMed ID: 4338447
    [Abstract] [Full Text] [Related]

  • 19. Studies in metachromatic leukodystrophy. XII. Multiple sulfatase deficiency.
    Austin JH.
    Arch Neurol; 1973 Apr 01; 28(4):258-64. PubMed ID: 4265903
    [No Abstract] [Full Text] [Related]

  • 20. Diagnostic techniques in metachromatic leukodystrophy.
    Julius R, Buehler B, Aylsworth A, Petery LS, Rennert O, Greer M.
    Neurology; 1971 Jan 01; 21(1):15-8. PubMed ID: 4099955
    [No Abstract] [Full Text] [Related]


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