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Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trial.
Amalfitano A, Bengur AR, Morse RP, Majure JM, Case LE, Veerling DL, Mackey J, Kishnani P, Smith W, McVie-Wylie A, Sullivan JA, Hoganson GE, Phillips JA 3rd, Schaefer GB, Charrow J, Ware RE, Bossen EH, Chen YT. Amalfitano A, et al. Genet Med. 2001 Mar-Apr;3(2):132-8. Genet Med. 2001. PMID: 11286229 Free article. Clinical Trial.
Pompe disease in infants and children.
Kishnani PS, Howell RR. Kishnani PS, et al. J Pediatr. 2004 May;144(5 Suppl):S35-43. doi: 10.1016/j.jpeds.2004.01.053. J Pediatr. 2004. PMID: 15126982 Review. No abstract available.
Electrocardiographic response to enzyme replacement therapy for Pompe disease.
Ansong AK, Li JS, Nozik-Grayck E, Ing R, Kravitz RM, Idriss SF, Kanter RJ, Rice H, Chen YT, Kishnani PS. Ansong AK, et al. Among authors: kishnani ps. Genet Med. 2006 May;8(5):297-301. doi: 10.1097/01.gim.0000195896.04069.5f. Genet Med. 2006. PMID: 16702879 Free article. Clinical Trial.
Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease.
Zhang H, Kallwass H, Young SP, Carr C, Dai J, Kishnani PS, Millington DS, Keutzer J, Chen YT, Bali D. Zhang H, et al. Among authors: kishnani ps. Genet Med. 2006 May;8(5):302-6. doi: 10.1097/01.gim.0000217781.66786.9b. Genet Med. 2006. PMID: 16702880 Free article.
Physical therapy management of Pompe disease.
Case LE, Kishnani PS. Case LE, et al. Among authors: kishnani ps. Genet Med. 2006 May;8(5):318-27. doi: 10.1097/01.gim.0000217789.14470.c5. Genet Med. 2006. PMID: 16702883 Free article. Review.
407 results