[Tay-Sachs disease with hexosaminidase deficiency. Clinical, morphological and biochemical findings in a case with visceral storage of renal globosides].

Tay-Sachssche Krankheit mit Hexosaminidase-Defekt. Klinische, morphologische und biochemische Bedunde bei einem Fall mit viszeraler Speicherung von Nierenglobosid.

Deutsche medizinische Wochenschrift (1946) ·Vol. 93 ·No. 39 ·1968-09-27 ·Pages 1833-9 passim

Pilz H, Müller D, Sandhoff K, ter Meulen V

Abstract

暂无摘要

MeSH Terms

Child, Preschool Deficiency Diseases/complications Glycolipids/analysis,metabolism Glycoside Hydrolases/metabolism Histocytochemistry Humans Kidney/analysis,metabolism,pathology Lipidoses/metabolism,pathology Liver/analysis,metabolism,pathology Male Spleen/analysis,metabolism

Chemicals

Glycolipids Glycoside Hydrolases

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Pilz H

Müller D

Sandhoff K

ter Meulen V

Article Info

Journal

Deutsche medizinische Wochenschrift (1946)

Abbr.

Dtsch Med Wochenschr

ISSN

0012-0472

DOI

10.1055/s-0028-1110836

Published

1968-09-27

Pages

1833-9 passim

Language

ger

Region

Germany

NLM ID

0006723

Subset

External Links

PubMed source DOI: 10.1055/s-0028-1110836 View journal details

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[Tay-Sachs disease with hexosaminidase deficiency. Clinical, morphological and biochemical findings in a case with visceral storage of renal globosides].

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