Literature DB >> 6214919

Fetal congenital lethal hypophosphatasia: histochemical absence of alkaline phosphatase activity in endothelial cells of intramuscular capillaries.

H H Goebel, M Schlie, U Burck.   

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Year:  1982        PMID： 6214919     DOI： 10.1007/bf00685396

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN： 0001-6322            Impact factor:   17.088


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  4 in total

1.  Becker's x-linked muscular dystrophy. Histological, enzyme-histochemical, and ultrastructural studies of two cases, originally reported by Becker.

Authors:  H H Goebel; H Prange; F Gullotta; H Kiefer; M Z Jones
Journal:  Acta Neuropathol       Date:  1979-04-12       Impact factor: 17.088

2.  Myoadenylate deaminase deficiency: a new disease of muscle.

Authors:  W N Fishbein; V W Armbrustmacher; J L Griffin
Journal:  Science       Date:  1978-05-05       Impact factor: 47.728

3.  Prenatal diagnosis of hypophosphatasia; genetic, biochemical, and clinical studies.

Authors:  R A Mulivor; M Mennuti; E H Zackai; H Harris
Journal:  Am J Hum Genet       Date:  1978-05       Impact factor: 11.025

4.  Muscle phosphorylase deficiency in childhood.

Authors:  R C Sengers; A M Stadhouders; H H Jaspar; K J Lamers; J M Trijbels; S L Notermans
Journal:  Eur J Pediatr       Date:  1980-08       Impact factor: 3.183
  4 in total

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