Literature DB >> 4565559

Histochemical and biochemical studies of urinary lipids in metachromatic leukodystrophy and Fabry's disease.

H Pilz, D Müller, I Linke.   

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Year:  1973        PMID： 4565559

Source DB:  PubMed          Journal:  J Lab Clin Med        ISSN： 0022-2143


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  4 in total

Review 1.  Basic findings and current developments in sphingolipidoses.

Authors:  H Pilz; R Heipertz; D Seidel
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

2.  Anderson-Fabry disease: rapid detection of carriers by hair bulb analysis.

Authors:  A Ejiofor; D Robinson; D Wise; M Hamers; J M Tager
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

3.  Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency.

Authors:  J Kappler; P Leinekugel; E Conzelmann; W J Kleijer; A Kohlschütter; T Tønnesen; M Rochel; F Freycon; P Propping
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

4.  Increased glycosphingolipid excretion associated with proteinuria.

Authors:  R R Townsend; R M Orth; C M Clawson; S C Li; Y T Li
Journal:  J Clin Invest       Date:  1978-07       Impact factor: 14.808
  4 in total

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