Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical and immunological study-Reference-Cited by-同舟云学术

Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical and immunological study

Published:1991-06 Issue:8 Volume:150 Page:584-591
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Schlote W.,Harzer K.,Christomanou H.,Paton B. C.,Kustermann-Kuhn B.,Schmid B.,Seeger J.,Beudt U.,Schuster I.,Langenbeck U.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF02072213.pdf

Reference40 articles.

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2. Baum H, Dodgson KS, Spencer B (1959) The assay of arylsulfatase A and B in human urine. Clin Chim Acta 4:453–455

3. Christomanou H, Kleinschmidt T (1985) Isolation of two forms of an activator protein for the enzymic sphingomyelin degradation from human Gaucher spleen. Biol Chem Hoppe Seyler 366:245–256

4. Christomanou H, Čáp C, Sandhoff K (1977) Isoelectric focusing pattern of acid hydrolases in cultured fibroblasts, leucocytes and cell-free amniotic fluid. Neuropädiatrie 8:238–252

5. Christomanou H, Aignesberger A, Linke RP (1986) Immunochemical characterization of two activator proteins stimulating enzymic sphingomyelin degradation in vitro. Absence of one of them in a human Gaucher disease variant. Biol Chem Hoppe Seyler 367:879–890

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