Skrinar AM - Search Results

1

A computer adaptive testing approach for assessing physical functioning in children and adolescents.

Haley SM, Ni P, Fragala-Pinkham MA, Skrinar AM, Corzo D. Haley SM, et al. Among authors: skrinar am. Dev Med Child Neurol. 2005 Feb;47(2):113-20. doi: 10.1017/s0012162205000204. Dev Med Child Neurol. 2005. PMID: 15707234 Free article.

2

Pompe disease and physical disability.

Haley SM, Fragala MA, Skrinar AM. Haley SM, et al. Among authors: skrinar am. Dev Med Child Neurol. 2003 Sep;45(9):618-23. doi: 10.1017/s0012162203001129. Dev Med Child Neurol. 2003. PMID: 12948329 Free article.

3

Development of a disease-specific disability instrument for Pompe disease.

Haley SM, Fragala MA, Aseltine R, Ni P, Skrinar AM. Haley SM, et al. Among authors: skrinar am. Pediatr Rehabil. 2003 Apr-Jun;6(2):77-84. doi: 10.1080/1363849031000139298. Pediatr Rehabil. 2003. PMID: 14534044

4

Pediatric physical functioning reference curves.

Haley SM, Fragala-Pinkham MA, Ni PS, Skrinar AM, Kaye EM. Haley SM, et al. Among authors: skrinar am. Pediatr Neurol. 2004 Nov;31(5):333-41. doi: 10.1016/j.pediatrneurol.2004.05.002. Pediatr Neurol. 2004. PMID: 15519114

5

A physical performance measure for individuals with mucopolysaccharidosis type I.

Haley SM, Fragala Pinkham MA, Dumas HM, Ni P, Skrinar AM, Cox GF. Haley SM, et al. Among authors: skrinar am. Dev Med Child Neurol. 2006 Jul;48(7):576-81. doi: 10.1017/S0012162206001216. Dev Med Child Neurol. 2006. PMID: 16780627 Free article.

6

The emerging role of the pediatric physical therapist in evaluation and intervention for individuals with lysosomal storage diseases.

Haley SM, Fragala-Pinkham M, Latham NK, Skrinar AM, Cogswell D. Haley SM, et al. Among authors: skrinar am. Pediatr Phys Ther. 2005 Summer;17(2):128-39. doi: 10.1097/01.pep.0000163077.26274.9c. Pediatr Phys Ther. 2005. PMID: 16357663 Review.

7

Physical performance testing in mucopolysaccharidosis I: a pilot study.

Dumas HM, Fragala MA, Haley SM, Skrinar AM, Wraith JE, Cox GF. Dumas HM, et al. Among authors: skrinar am. Pediatr Rehabil. 2004 Apr-Jun;7(2):125-31. doi: 10.1080/13638490310001654763. Pediatr Rehabil. 2004. PMID: 15204583

8

Rapid diagnosis of late-onset Pompe disease by fluorometric assay of alpha-glucosidase activities in dried blood spots.

Kallwass H, Carr C, Gerrein J, Titlow M, Pomponio R, Bali D, Dai J, Kishnani P, Skrinar A, Corzo D, Keutzer J. Kallwass H, et al. Mol Genet Metab. 2007 Apr;90(4):449-52. doi: 10.1016/j.ymgme.2006.12.006. Epub 2007 Jan 31. Mol Genet Metab. 2007. PMID: 17270480

9

Clinical features of late-onset Pompe disease: a prospective cohort study.

Wokke JH, Escolar DM, Pestronk A, Jaffe KM, Carter GT, van den Berg LH, Florence JM, Mayhew J, Skrinar A, Corzo D, Laforet P. Wokke JH, et al. Muscle Nerve. 2008 Oct;38(4):1236-45. doi: 10.1002/mus.21025. Muscle Nerve. 2008. PMID: 18816591

10

A randomized study of alglucosidase alfa in late-onset Pompe's disease.

van der Ploeg AT, Clemens PR, Corzo D, Escolar DM, Florence J, Groeneveld GJ, Herson S, Kishnani PS, Laforet P, Lake SL, Lange DJ, Leshner RT, Mayhew JE, Morgan C, Nozaki K, Park DJ, Pestronk A, Rosenbloom B, Skrinar A, van Capelle CI, van der Beek NA, Wasserstein M, Zivkovic SA. van der Ploeg AT, et al. N Engl J Med. 2010 Apr 15;362(15):1396-406. doi: 10.1056/NEJMoa0909859. N Engl J Med. 2010. PMID: 20393176 Free article. Clinical Trial.

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