Literature DB >> 6133037

Neonatal multiple sulphatase deficiency disorder: biochemical characterization.

Y Eto, T Tokoro, Y Kureha, N Koda, Y Tada, T Tahara, K Maekawa, I Liebaers, E Vamos.   

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Year:  1982        PMID： 6133037     DOI： 10.1007/bf02179152

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  6 in total

1.  The assay of arylsulphatases A and B in human urine.

Authors:  H BAUM; K S DODGSON; B SPENCER
Journal:  Clin Chim Acta       Date:  1959-05       Impact factor: 3.786

2.  Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy.

Authors:  Y Eto; U N Wiesmann; J H Carson; N N Herschkowitz
Journal:  Arch Neurol       Date:  1974-02

3.  The defect in Hurler and Hunter syndromes. II. Deficiency of specific factors involved in mucopolysaccharide degradation.

Authors:  J C Fratantoni; C W Hall; E F Neufeld
Journal:  Proc Natl Acad Sci U S A       Date:  1969-09       Impact factor: 11.205

4.  Multiple sulphatase deficiency with early onset.

Authors:  E Vamos; I Liebaers; N Bousard; J Libert; N Perlmutter
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

5.  Thiosulfate-mediated increase of arylsulfatase activities in multiple sulfatase deficiency disorder fibroblasts.

Authors:  H Kresse; D Holtfrerich
Journal:  Biochem Biophys Res Commun       Date:  1980-11-17       Impact factor: 3.575

6.  Multiple sulfatase deficiency (mucosulfatidosis): impaired degradation of labeled sulfated compounds in cultured skin fibroblasts in vivo.

Authors:  Y Eto; S Numaguchi; T Tahara; O M Rennert
Journal:  Eur J Pediatr       Date:  1980-10       Impact factor: 3.183
  6 in total

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