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scopus: 35318086600

Li, J.S.

(Jennifer Li)


disease patient pompe pompe disease late-onset pompe disease study enzyme replacement therapy baseline enzyme late-onset treatment abnormality replacement mass index therapy hypertrophy group echocardiogram center duration signi interval ejection echocardiographic fraction ejection fraction ficant analysis 0.99 alpha-glucosidase index university glycogen control acid alpha-glucosidase treatment arm 78 weeks range change safety block van der ploeg tachycardia enzyme replacement number infantile-onset pompe disease medicine ef ficacy pr interval abnormalities identi fied children wolff-parkinson-white syndrome adult variable kishnani bundle branch volume genetic hospital table placebo signi ficant syndrome van doorn p storage signi ficant change trial genet identi pediatr status parameter interquartile range echocardiographic abnormalities function 78- ficacy disease duration echocardiography




2 Most Recent Publications

Cardiovascular abnormalities in late-onset Pompe disease and response to enzyme replacement therapy (Article)
Forsha, D. Li, J.S. Smith, P.B. Ploeg, A.T. van der Kishnani, P.S. Pasquali, S.K.
2011-07-01
Recombinant human acid α-glucosidase: Major clinical benefits in infantile-onset Pompe disease (Article)
Kishnani, P.S. Corzo, D. Li, J.S. Dumontier, J. Halberthal, M. Chien, Y.H. Hopkin, R. Vijayaraghavan, S. Gruskin, D. Bartholomew, D. Ploeg, A.T. van der Clancy, J.P. Nicolino, M. Parini, R. Morin, G. Beck, M. La Gastine, G.S. de Jokic, M. Thurberg, B. Richards, S. Bali, D. Davison, M. Worden, M.A. Byrne, B. Chen, Y.T. Wraith, J.E. Mandel, H. Hwu, W.L. Leslie, N. Levine, J. Spencer, C. McDonald, M.
2007-01-01