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教育部委託研究計畫      計畫執行:國立臺灣大學圖書館
 
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機構 日期 題名 作者
臺大學術典藏 2020-12-24T06:16:36Z Congenital malformations in newborns - A challenge unmet for decades Hwu W.-L.; YIN-HSIU CHIEN; Lee N.-C.
臺大學術典藏 2020-12-24T06:16:35Z Advances in newborn screening for Pompe disease and resulting clinical outcomes YIN-HSIU CHIEN; Hwu W.-L.; Lee N.-C.
臺大學術典藏 2020-12-24T06:16:34Z Slow, progressive myopathy in neonatally treated patients with infantile-onset Pompe disease: A muscle magnetic resonance imaging study Dr. Segolene Ayme Dr. Segolene Ayme YIN-HSIU CHIEN; Tsai W.-H.; Tsai F.-J.; Lee N.-C.; Hwu W.-L.; Peng S.S.-F.
臺大學術典藏 2020-12-24T06:16:33Z 3-O-methyldopa levels in newborns: Result of newborn screening for aromatic L-amino-acid decarboxylase deficiency YIN-HSIU CHIEN; Chen P.-W.; Lee N.-C.; Hsieh W.-S.; Chiu P.-C.; Hwu W.-L.; Tsai F.-J.; Lin S.-P.; Chu S.-Y.; Jong Y.-J.; Chao M.-C.
臺大學術典藏 2020-12-24T06:16:32Z Genetic epidemiological study doesn't support GLA IVS4?+?919G?>?A variant is a significant mutation in Fabry disease Hwu W.-L.; YIN-HSIU CHIEN; Wen M.-S.; Song I.-W.; Chang C.-P.; Wang N.H.-H.; Chiang H.-L.; Tsai F.-J.; Chen Y.-T.; Wu J.-Y.
臺大學術典藏 2020-12-24T06:16:32Z Blood beta-amyloid and tau in down syndrome: A comparison with Alzheimer's disease Chiu M.-J.; Hwu W.-L.; YIN-HSIU CHIEN; Huang A.-C.; Lee N.-C.; Yang S.-Y.; Chieh J.-J.; Huang P.-T.; Chang L.-M.; Chiu Y.-N.
臺大學術典藏 2020-12-24T06:16:31Z Longitudinal follow-up to evaluate speech disorders in early-treated patients with infantile-onset Pompe disease Zeng Y.-T.; Hwu W.-L.; Torng P.-C.; Lee N.-C.; Shieh J.-Y.; Lu L.; YIN-HSIU CHIEN
臺大學術典藏 2020-12-24T06:16:31Z Albuterol as an adjunctive treatment to enzyme replacement therapy in infantile-onset Pompe disease YIN-HSIU CHIEN; Hwu W.-L.; Lee N.-C.; Tsai F.-J.; Koeberl D.D.; Tsai W.-H.; Chiu P.-C.; Chang C.-L.
臺大學術典藏 2020-12-24T06:16:29Z Presymptomatic Diagnosis of Spinal Muscular Atrophy Through Newborn Screening YIN-HSIU CHIEN; Chiang S.-C.; Weng W.-C.; Lee N.-C.; Lin C.-J.; Hsieh W.-S.; Lee W.-T.; Jong Y.-J.; Ko T.-M.; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:28Z Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency detected by neonatal screening Liu S.-Y.; Lee C.-T.; Tung Y.-C.; YIN-HSIU CHIEN; Hwu W.-L.; Tsai W.-Y.

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