Similar articles

• Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures.

  Porter MT, Fluharty AL, Kihara H. Porter MT, et al. Proc Natl Acad Sci U S A. 1969 Mar;62(3):887-91. doi: 10.1073/pnas.62.3.887. Proc Natl Acad Sci U S A. 1969. PMID: 5257010 Free PMC article.
• Diagnostic techniques in metachromatic leukodystrophy.

  Julius R, Buehler B, Aylsworth A, Petery LS, Rennert O, Greer M. Julius R, et al. Neurology. 1971 Jan;21(1):15-8. doi: 10.1212/wnl.21.1.15. Neurology. 1971. PMID: 4099955 No abstract available.
• Late adult metachromatic leukodystrophy. Arylsulfatase A activity of leukocytes in two families.

  Pilz H. Pilz H. Arch Neurol. 1972 Jul;27(1):87-90. doi: 10.1001/archneur.1972.00490130089013. Arch Neurol. 1972. PMID: 5049684 No abstract available.
• Prenatal genetic diagnosis (second of three parts).

  Milunsky A, Littlefield JW, Kanfer JN, Kolodny EH, Shih VE, Atkins L. Milunsky A, et al. N Engl J Med. 1970 Dec 24;283(26):1441-7. doi: 10.1056/NEJM197012242832605. N Engl J Med. 1970. PMID: 4098222 Review. No abstract available.
• The use of white cells as a source of diagnostic material for lipid storage diseases.

  Snyder RA, Brady RO. Snyder RA, et al. Clin Chim Acta. 1969 Aug;25(2):331-8. doi: 10.1016/0009-8981(69)90275-7. Clin Chim Acta. 1969. PMID: 4895581 Review. No abstract available.