α-Glucosidase in Pompe's disease
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01805584
Reference8 articles.
1. Bøyum, A. (1968). Isolation of mononuclear cells and granulocytes from human blood.Scand. J. Clin. Lab. Invest.,21, Suppl. 97, 77
2. Broadhead, D. M. and Butterworth, J. (1978). Pompe's disease: diagnosis in kidney and leucocytes using 4-methyl-umbelliferyl-α-D-glucopyranoside.Clin. Genet.,13, 504
3. Huijing, F., van Creveld, S. and Losekoot, G. (1963). Diagnosis of generalized glycogen storage disease (Pompe's disease).J. Pediatr.,63, 984
4. Koster, J. F., Slee, R. G. and Hülsman, W. C. (1974). The use of leucocytes as an aid in the diagnosis of glycogen storage disease type II (Pompe's disease).Clin. Chim. Acta,51, 319
5. Koster, J. F., Slee, R. G., van der Klei-van Moorsel, J. M., Rietra, P. J. G. M. and Lucas, C. J. (1976). Physico-chemical and immunological properties of acid α-glucosidase from various human tissues in relation to glycogenosis type II (Pompe's disease).Clin. Chim. Acta,68, 49
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2. Enhanced delivery of α-glucosidase for Pompe disease by ICAM-1-targeted nanocarriers: comparative performance of a strategy for three distinct lysosomal storage disorders;Nanomedicine: Nanotechnology, Biology and Medicine;2012-07
3. Alpha-glucosidase deficiency and basilar artery aneurysm: Report of a sibship;Annals of Neurology;1987-11
4. The “muscular variant” of Pompe disease: Clinical, biochemical and histologic characteristics;American Journal of Medical Genetics;1985-07
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