Literature DB >> 1022088

[Adult Niemann-Pick disease (author's transl)].

W Wegmann, R Siebenmann, R Ammann.   

Abstract

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Year:  1976        PMID： 1022088

Source DB:  PubMed          Journal:  Verh Dtsch Ges Pathol        ISSN： 0070-4113


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  2 in total

1.  A new variant of sphingomyelinase deficiency (Niemann-Pick): visceromegaly, minimal neurological lesions and low in vivo degradation rate of sphingomyelin.

Authors:  M Elleder; J Nevoral; V Spicáková; H Hyniová; J Kraus; J Krásný; M T Vanier
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

2.  Niemann-Pick disease (variation in the sphingomyelinase deficient group). Neurovisceral phenotype (A) with an abnormally protracted clinical course and variable expression of neurological symptomatology in three siblings.

Authors:  M Elleder; J Cihula
Journal:  Eur J Pediatr       Date:  1983-09       Impact factor: 3.183
  2 in total

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