A new diagnostic assay for glycogen storage disease type II in mixed leukocytes-Reference-Cited by-同舟云学术

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A new diagnostic assay for glycogen storage disease type II in mixed leukocytes

Published:2006-05 Issue:1 Volume:88 Page:22-28
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Okumiya Toshika,Keulemans Joke L.M.,Kroos Marian A.,Van der Beek Nadine M.E.,Boer Marijke A.,Takeuchi Hiroaki,Van Diggelen Otto P.,Reuser Arnold J.J.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference26 articles.

1. Glycogen storage disease type II: acid α-glucosidase (acid maltase) deficiency;Hirschhorn,2001

2. The use of leucocytes as an aid in the diagnosis of glycogen storage disease type II (Pompe’s disease);Koster;Clin. Chim. Acta,1974

3. Alpha glucosidases in white blood cells with reference to the detection of acid α 1–4 glucosidase deficiency;Dreyfus;Biochem. Biophys. Res. Commun.,1978

4. White blood cells and the diagnosis of α-glucosidase deficiency;Dreyfus;Pediatr. Res.,1980

5. Neutral α-glucosidase from human kidney. Molecular and immunological properties. Relationship with intestinal glucoamylase;de Burlet;Biochimie.,1979

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