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Journal Abstract Search
110 related items for PubMed ID: 5538094
1. Metachromatic leucodystrophy. Assay of arylsulfatase activities in the urine. Hagberg B, Ockerman PA. Neuropadiatrie; 1970 Aug; 2(1):53-8. PubMed ID: 5538094 [No Abstract] [Full Text] [Related]
2. Studies on arylsulfatase-A activity in metachromatic leucodystrophy. Komiya K, Arima M. Paediatr Univ Tokyo; 1970 Dec; 18():99-104. PubMed ID: 5535257 [No Abstract] [Full Text] [Related]
3. [Determination of arylsulfatase activity in urine. Clinical significance]. Humbel R, Marchal C, Fall M. Ann Pediatr (Paris); 1968 Oct 02; 15(10):632-4. PubMed ID: 4237830 [No Abstract] [Full Text] [Related]
4. [Familial metachromatic leucodystrophy--arylsulfatase A activity of leukocytes and probable carrier state]. Nanba K, Taniguchi N. Nihon Shonika Gakkai Zasshi; 1970 Jun 02; 74(6):590-5. PubMed ID: 5465441 [No Abstract] [Full Text] [Related]
5. Metachromatic leukodystrophy (MLD). IX. Qualitative and quantitative differences in urinary arylsulfatase A in different forms of MLD. Stumpf D, Austin J. Arch Neurol; 1971 Feb 02; 24(2):117-24. PubMed ID: 5540376 [No Abstract] [Full Text] [Related]
6. Arylsulfatase A in the urine and metachromatic leukodystrophy. Greene H, Hug G, Schubert WK. J Pediatr; 1967 Nov 02; 71(5):709-11. PubMed ID: 6054756 [No Abstract] [Full Text] [Related]
7. [Arylsulfatase A activity determination in urine and leukocytes]. Loyer D, Farriaux JP. Lille Med; 1972 Nov 02; 17(6):894-900. PubMed ID: 5085389 [No Abstract] [Full Text] [Related]
8. Metachromatic leucodystrophy in early childhood. Treatment with a diet deficient in vitamin A. Melchior JC, Clausen J. Acta Paediatr Scand; 1968 Jan 02; 57(1):2-8. PubMed ID: 5637009 [No Abstract] [Full Text] [Related]
11. Late adult metachromatic leukodystrophy. Arylsulfatase A activity of leukocytes in two families. Pilz H. Arch Neurol; 1972 Jul 02; 27(1):87-90. PubMed ID: 5049684 [No Abstract] [Full Text] [Related]
12. 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 02; 36(1):99-103. PubMed ID: 5007723 [No Abstract] [Full Text] [Related]
13. Metachromatic leucodystrophy. Two unusual cases of the late infantile form. Nyberg-Hansen R. Z Neurol; 1972 Jan 02; 203(2):145-54. PubMed ID: 4119025 [No Abstract] [Full Text] [Related]
17. Deficiency of arylsulfatase A in juvenile metachromatic leucodystrophy: fibroblast studies. Leroy JG, Van Elsen A, Dumon JE, Radermecker J. Monogr Hum Genet; 1972 Jan 02; 6():148-9. PubMed ID: 4663890 [No Abstract] [Full Text] [Related]
18. Metachromatic leukodystrophy: diagnosis with samples of venous blood. Percy AK, Brady RO. Science; 1968 Aug 09; 161(3841):594-5. PubMed ID: 5668537 [Abstract] [Full Text] [Related]
19. 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 09; 2(4):461-9. PubMed ID: 5171491 [No Abstract] [Full Text] [Related]