Literature DB >> 6820428

Prenatal diagnosis of metachromatic leukodystrophy: a diagnosis with amniotic fluid by DEAE-Sepharose column chromatography and its confirmation by kidney lipid analysis.

Y Eto, T Tahara, N Koda, S Yamaguchi.   

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Year:  1982        PMID： 6820428     DOI： 10.1007/bf01799995

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


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  4 in total

1.  Enzymic studies of sulphatases in tissues of the normal human and in metachromatic leukodystrophy with multiple sulphatase deficiencies: arylsulphatases A, B and C, cerebroside sulphatase, psychosine sulphatase and steroid sulphatases.

Authors:  Y Eto; S Rampini; U Wiesmann; N N Herschkowitz
Journal:  J Neurochem       Date:  1974-12       Impact factor: 5.372

2.  [Prenatal diagnosis of a case of metachromatic leucodystrophy (author's transl)].

Authors:  K Harzer; V Zahn; S Stengel-Rutkowski; E O Gley
Journal:  Dtsch Med Wochenschr       Date:  1975-04-25       Impact factor: 0.628

3.  Globoid cell leukodystrophy (Krabbe's disease): isolation of myelin with normal glycolipid composition.

Authors:  Y Eto; K Suzuki; K Suzuki
Journal:  J Lipid Res       Date:  1970-09       Impact factor: 5.922

4.  Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts.

Authors:  A L Fluharty; R L Stevens; D L Sanders; H Kihara
Journal:  Biochem Biophys Res Commun       Date:  1974-07-24       Impact factor: 3.575
  4 in total

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