Literature DB >> 5706652

Tissue acid hydrolase activities in Gaucher's disease.

P A Ockerman, P Köhlin.   

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Year:  1968        PMID: 5706652     DOI: 10.3109/00365516809160739

Source DB:  PubMed          Journal:  Scand J Clin Lab Invest        ISSN: 0036-5513            Impact factor:   1.713


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  8 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.  Infantile neurological Gaucher's disease in three siblings. An ultrastructural study.

Authors:  F Hernández; M Bueno
Journal:  Virchows Arch A Pathol Pathol Anat       Date:  1973

3.  Deficiency of alpha-mannosidase in Angus cattle. An inherited lysosomal storage disease.

Authors:  J D Hocking; R D Jolly; R D Batt
Journal:  Biochem J       Date:  1972-06       Impact factor: 3.857

4.  Beta-glucosidase activity in fibroblasts from homozygotes and heterozygotes for Gaucher's disease.

Authors:  E Beutler; W Kuhl; F Trinidad; R Teplitz; H Nadler
Journal:  Am J Hum Genet       Date:  1971-01       Impact factor: 11.025

5.  Newer aspects of some interesting lipid storage diseases: Tay-Sachs and Gaucher's diseases.

Authors:  E Beutler
Journal:  West J Med       Date:  1977-01

6.  In utero diagnosis of Gaucher disease.

Authors:  T Kitagawa; M Owada; T Sakiyama; K Aoki; S Kamoshita; Y Amenomori; T Kobayashi
Journal:  Am J Hum Genet       Date:  1978-05       Impact factor: 11.025

7.  Identity of 'acid' beta-glucosidase and glucocerebrosidase in human spleen.

Authors:  M W Ho
Journal:  Biochem J       Date:  1973-11       Impact factor: 3.857

8.  Gargoylism: hydrolysis of beta-galactosides and tissure accumulation of galactose- and mannose-containing compounds.

Authors:  B Hultberg; P A Ockerman; A Dahlqvist
Journal:  J Clin Invest       Date:  1970-02       Impact factor: 14.808

  8 in total

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