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Showing items 401-410 of 770  (77 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-12-09T01:38:25Z Diagnosis of aromatic l-amino acid decarboxylase deficiency by measuring 3-O-methyldopa concentrations in dried blood spots Chen P.-W.; NI-CHUNG LEE; Chien Y.-H.; Wu J.-Y.; Wang P.-C.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:25Z Treatment of congenital neurotransmitter deficiencies by intracerebral ventricular injection of an adeno-associated virus serotype 9 vector NI-CHUNG LEE; Chien Y.-H.; Hu M.-H.; Liu W.-S.; Chen P.-W.; Wang W.-H.; Tzen K.-Y.; Byrne B.J.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:25Z Prominent vacuolation of the eyelid levator muscle in an early-treated child with infantile-onset Pompe disease Chien Y.-H.;Ni-Chung Lee;Tsai Y.-J.;Thurberg B.L.;Tsai F.-J.;Hwu W.-L.; Chien Y.-H.; NI-CHUNG LEE; Tsai Y.-J.; Thurberg B.L.; Tsai F.-J.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:24Z Long-term prognosis of patients with infantile-onset pompe disease diagnosed by newborn screening and treated since birth Chien Y.-H.; NI-CHUNG LEE; Chen C.-A.; Tsai F.-J.; Tsai W.-H.; Shieh J.-Y.; Huang H.-J.; Hsu W.-C.; Tsai T.-H.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:24Z Baseline urinary glucose tetrasaccharide concentrations in patients with infantile- and late-onset pompe disease identified by newborn screening Chien Y.-H.; Goldstein J.L.; Hwu W.-L.; Smith P.B.; NI-CHUNG LEE; Chiang S.-C.; Tolun A.A.; Zhang H.; Vaisnins A.E.; Millington D.S.; Kishnani P.S.; Young S.P.
臺大學術典藏 2020-12-09T01:38:24Z Congenital malformations in newborns - A challenge unmet for decades NI-CHUNG LEE; Chien Y.-H.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:23Z Advances in newborn screening for Pompe disease and resulting clinical outcomes Chien Y.-H.; Hwu W.-L.; NI-CHUNG LEE
臺大學術典藏 2020-12-09T01:38:23Z Benefits of Neuronal Preferential Systemic Gene Therapy for Neurotransmitter Deficiency NI-CHUNG LEE; Muramatsu S.-I.; Chien Y.-H.; Liu W.-S.; Wang W.-H.; Cheng C.-H.; Hu M.-K.; Chen P.-W.; Tzen K.-Y.; Byrne B.J.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:23Z Mortality, disability, and intensive care in patients with mitochondrial 3243A>G mutation Hsiue H.-C.; NI-CHUNG LEE; Tsai H.-B.; Yang C.-C.; Wu C.-S.; Lee W.-T.; Weng W.-C.; Fan P.-C.; Chien Y.-H.; Hwu W.-L.; Hung K.-L.; Huang C.-C.; Chen C.-H.; Lin S.-J.; Chu S.-Y.; Wang T.-J.; Lu C.-J.; Lee P.-L.
臺大學術典藏 2020-12-09T01:38:22Z Slow, progressive myopathy in neonatally treated patients with infantile-onset Pompe disease: A muscle magnetic resonance imaging study Dr. Segolene Ayme Dr. Segolene Ayme Peng S.S.-F.; Hwu W.-L.; NI-CHUNG LEE; Tsai F.-J.; Tsai W.-H.; Chien Y.-H.

Showing items 401-410 of 770  (77 Page(s) Totally)
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