Glycogen accumulation in smooth muscle of a Pompe disease mouse model
Author:
Affiliation:
1. Division of Pulmonary Medicine, Department of Pediatrics, School of Medicine, Duke University, Durham, NC 27710, USA
Publisher
Japan Society of Smooth Muscle Research
Subject
General Medicine,Physiology
Link
https://www.jstage.jst.go.jp/article/jsmr/57/0/57_0516/_pdf
Reference54 articles.
1. 1. Hers, HG. alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe’s disease). Biochem J. 1963; 86: 11–6.
2. 2. Byrne, BJ, Kishnani, PS, Case, LE, Merlini, L, Müller-Felber, W, Prasad, S, van der Ploeg, A. Pompe disease: design, methodology, and early findings from the Pompe Registry. Mol Genet Metab. 2011; 103(1): 1–11.
3. 3. Kishnani, PS, Hwu, WL, Mandel, H, Nicolino, M, Yong, F, Corzo, D, Infantile-Onset Pompe Disease Natural History Study. Group A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease. J Pediatr. 2006; 148(5): 671–6.
4. 4. DeRuisseau, LR, Fuller, DD, Qiu, K, DeRuisseau, KC, Donnelly, WHJr , Mah, C, Reier, PJ, Byrne, BJ. Neural deficits contribute to respiratory insufficiency in Pompe disease. Proc Natl Acad Sci USA. 2009; 106(23): 9419–24.
5. 5. van den Hout, HMP, Hop, W, van Diggelen, OP, Smeitink, JAM, Smit, GPA, Poll-The, BTT, Bakker, HD, Loonen, MCB, de Klerk, JBC, Reuser, AJJ, van der Ploeg, AT. The natural course of infantile Pompe’s disease: 20 original cases compared with 133 cases from the literature. Pediatrics. 2003; 112(2): 332–40.
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