Literature DB >> 4715673

An activator of cerebroside sulphatase in human normal liver and in cases of congenital metachromatic leukodystrophy.

H Jatzkewitz, K Stinshoff.   

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Year:  1973        PMID： 4715673     DOI： 10.1016/0014-5793(73)80754-9

Source DB:  PubMed          Journal:  FEBS Lett        ISSN： 0014-5793            Impact factor:   4.124


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  5 in total

1.  [Sphingolipid storage disease as an example of a molecular neuropathology (author's transl)].

Authors:  H Jatzkewitz; K Sandhoff
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1976-04-30

2.  Sphingolipidoses.

Authors:  K Sandhoff
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974

3.  Sulfatide excreting heterozygous carrier of juvenile metachromatic leukodystrophy or asymptomatic patient of adult metachromatic leukodystrophy.

Authors:  K Harzer; A S Recke
Journal:  Humangenetik       Date:  1975-10-07

4.  Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophy.

Authors:  R L Stevens; A L Fluharty; H Kihara; M M Kaback; L J Shapiro; B Marsh; K Sandhoff; G Fischer
Journal:  Am J Hum Genet       Date:  1981-11       Impact factor: 11.025

5.  Concentrations of an activator protein for sphingolipid hydrolysis in liver and brain samples from patients with lysosomal storage diseases.

Authors:  K Inui; D A Wenger
Journal:  J Clin Invest       Date:  1983-11       Impact factor: 14.808
  5 in total

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