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| 臺大學術典藏 |
2019-09-09T00:55:33Z |
GAA variants and phenotypes among 1,079 patients with Pompe disease: Data from the Pompe Registry
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Llerena, Juan;YIN-HSIU CHIEN;Kishnani, Priya S.;Araujo, Roberto;Toscano, Antonio;Clemens, Paula R.;Maruti, Sonia S.;Periquet, Magali;Leslie, Nancy;Reuser, Arnold J.J.;Kimonis, Virginia E.;Sanson, Bernd Jan;Abbott, Mary Alice;van der Ploeg, Ans T.; van der Ploeg, Ans T.; Abbott, Mary Alice; Sanson, Bernd Jan; Kimonis, Virginia E.; Reuser, Arnold J.J.; Leslie, Nancy; Periquet, Magali; Maruti, Sonia S.; Clemens, Paula R.; Toscano, Antonio; Araujo, Roberto; Kishnani, Priya S.; YIN-HSIU CHIEN; Llerena, Juan |
| 國立臺灣大學 |
2014 |
Survival and developmental milestones among Pompe registry patients with classic infantile-onset Pompe disease with different timing of initiation of treatment with enzyme replacement therapy (ERT)
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Chien, Yin-Hsiu; van der Ploeg, Ans; Jones, Simon A.; Byrne, Barry; Vellodi, Ashok; Leslie, Nancy; Mengel, Eugen; Shankar, Suma; Tanpaiboon, Pranoot; Stockton, David W.; Hennermann, Julia B.; Devecseri, Zsuzsanna; Kempf, Judy; Keutzer, Joan; Kishnani, Priya S.; 簡穎秀 |
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