Author:
Lim Han-Hyuk,Yi Haiqing,Kishimoto Takashi K.,Gao Fengqin,Sun Baodong,Kishnani Priya S.
Subject
Endocrinology,Genetics,Molecular Biology
Reference35 articles.
1. The new era of Pompe disease: advances in the detection, understanding of the phenotypic spectrum, pathophysiology, and management;Kishnani;Am. J. Med. Genet. C: Semin. Med. Genet.,2012
2. Glycogen storage disease type II: acid a-glucosidase (acid maltase) deficiency;Hirschhorn,2009
3. Infantile-Onset Pompe Disease Natural History Study, a retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease;Kishnani;J. Pediatr.,2006
4. Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease;Nicolino;Genitourin. Med.,2009
5. Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe disease;Kishnani;Neurology,2007
Cited by
23 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献