Literature DB >> 5049680

Niemann-Pick disease (Crocker's group A). Late onset and pigmentary degeneration resembling Hallervorden-Spatz syndrome.

J J Martin, M Philippart, J Van Hauwaert, J W Callahan, R Deberdt.   

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Year:  1972        PMID： 5049680     DOI： 10.1001/archneur.1972.00490130047007

Source DB:  PubMed          Journal:  Arch Neurol        ISSN： 0003-9942


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  11 in total

1.  Niemann-Pick disease (Crocker's type C): A histological study of the distribution and qualitative differences fo the storage process.

Authors:  M Elleder; A Jirásek; F Smíd
Journal:  Acta Neuropathol       Date:  1975-12-19       Impact factor: 17.088

2.  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

3.  Low and moderate concentrations of lysobisphosphatidic acid in brain and liver of patients affected by some storage diseases.

Authors:  K Kahma; J Brotherus; M Haltia; O Renkonen
Journal:  Lipids       Date:  1976-07       Impact factor: 1.880

4.  Niemann-Pick disease type C. Study on the nature of the cerebral storage process.

Authors:  M Elleder; A Jirásek; F Smíd; J Ledvinová; G T Besley
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

5.  Deficiency of taurocholate-dependent phospholipase C acting on phosphatidylcholine in Niemann-Pick disease.

Authors:  J R Wherrett; S Huterer
Journal:  Neurochem Res       Date:  1983-01       Impact factor: 3.996

6.  An unusual case of phospholipidosis.

Authors:  M Elleder; A Jirásek; F Smíd; K Harzer; D Schlegerová
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1978-04-17

7.  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

8.  Cultured skin fibroblasts in storage disorders. An analysis of ultrastructural features.

Authors:  E Kamensky; M Philippart; P Cancilla; S P Frommes
Journal:  Am J Pathol       Date:  1973-10       Impact factor: 4.307

Review 9.  Secondary lipid accumulation in lysosomal disease.

Authors:  Steven U Walkley; Marie T Vanier
Journal:  Biochim Biophys Acta       Date:  2008-12-09

10.  A case of Kufs disease with abnormal pallidonigral iron deposit.

Authors:  S Galatioto; S Serra; R Di Perri; V Cavallari; D Villari; R Musolino
Journal:  Ital J Neurol Sci       Date:  1985-06
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