Detalhe da pesquisa
1.
A randomized study of alglucosidase alfa in late-onset Pompe's disease.
N Engl J Med
; 362(15): 1396-406, 2010 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20393176
2.
The quick motor function test: a new tool to rate clinical severity and motor function in Pompe patients.
J Inherit Metab Dis
; 35(2): 317-23, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21912959
3.
Fontan Circulation Associated Organ Abnormalities Beyond the Heart, Lungs, Liver, and Gut: A Systematic Review.
Front Cardiovasc Med
; 9: 826096, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35391839
4.
Gingival overgrowth in Pompe disease: a case report.
J Oral Maxillofac Surg
; 69(8): 2186-90, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21783002
5.
Hearing loss in Pompe disease revisited: results from a study of 24 children.
J Inherit Metab Dis
; 33(5): 597-602, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20596893
6.
PAS-positive lymphocyte vacuoles can be used as diagnostic screening test for Pompe disease.
J Inherit Metab Dis
; 33(2): 133-9, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20107902
7.
Cardiac outcome in classic infantile Pompe disease after 13â¯years of treatment with recombinant human acid alpha-glucosidase.
Int J Cardiol
; 269: 104-110, 2018 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30049495
8.
Low bone mass in Pompe disease: muscular strength as a predictor of bone mineral density.
Bone
; 47(3): 643-9, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20601298
9.
Both type 1 and type 2a muscle fibers can respond to enzyme therapy in Pompe disease.
Muscle Nerve
; 37(2): 251-5, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17894362