Literature DB >> 4698279

The patterns of arylsulphatases A and B in human normal and metachromatic leucodystrophy tissues and their relationship to the cerebroside sulphatase activity.

K Harzer, K Stinshoff, W Mraz, H Jatzkewitz.   

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Year:  1973        PMID： 4698279     DOI： 10.1111/j.1471-4159.1973.tb12127.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN： 0022-3042            Impact factor:   5.372


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  5 in total

1.  [Preliminary results in the prenatal diagnosis of Tay-Sachs disease by isoelectric focusing of hexosaminidase A (author's transl)].

Authors:  K Harzer
Journal:  Klin Wochenschr       Date:  1974-02-01

2.  Inheritance of the enzyme deficiency in three neurolipidoses: variant 0 of Tay-Sachs disease (Sandhoff's disease), classic Tay-Sachs disease, and metachromatic leukodystrophy. Identification of the heterozygous carriers.

Authors:  K Harzer
Journal:  Humangenetik       Date:  1973

3.  Sphingolipidoses.

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

4.  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

5.  Novel patient cell-based HTS assay for identification of small molecules for a lysosomal storage disease.

Authors:  Haifeng Geng; Grace Whiteley; Jameson Ribbens; Wei Zheng; Noel Southall; Xin Hu; Juan J Marugan; Marc Ferrer; Gustavo H B Maegawa
Journal:  PLoS One       Date:  2011-12-21       Impact factor: 3.240
  5 in total

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