English  |  正體中文  |  简体中文  |  总笔数 :0  
造访人次 :  50691845    在线人数 :  243
教育部委托研究计画      计画执行:国立台湾大学图书馆
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
关于TAIR

浏览

消息

著作权

相关连结

"hwu w l"的相关文件

回到依作者浏览
依题名排序 依日期排序

显示项目 251-260 / 770 (共77页)
<< < 21 22 23 24 25 26 27 28 29 30 > >>
每页显示[10|25|50]项目

机构 日期 题名 作者
臺大學術典藏 2020-12-24T06:16:38Z Diagnosis of aromatic l-amino acid decarboxylase deficiency by measuring 3-O-methyldopa concentrations in dried blood spots Chen P.-W.; Lee N.-C.; YIN-HSIU CHIEN; Wu J.-Y.; Wang P.-C.; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:37Z Long-term prognosis of patients with infantile-onset pompe disease diagnosed by newborn screening and treated since birth Tsai F.-J.; Chen C.-A.; Lee N.-C.; YIN-HSIU CHIEN; Tsai W.-H.; Shieh J.-Y.; Huang H.-J.; Hsu W.-C.; Tsai T.-H.; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:37Z Incidence of severe combined immunodeficiency through newborn screening in a Chinese population Yu H.-H.; Chang K.-L.; Chiang S.-C.; YIN-HSIU CHIEN; Lee W.-I.; Tsai L.-P.; Hsu L.-W.; Hu M.-H.; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:36Z Mudd's disease (MAT I/III deficiency): A survey of data for MAT1A homozygotes and compound heterozygotes Raymond K.; Okano Y.; Muntau A.; Mayatepek E.; Lindner M.; Lykopoulou L.; Levy H.; Lachmann R.; Korman S.H.; Kim S.; YIN-HSIU CHIEN; Abdenur J.E.; Baronio F.; Bannick A.A.; Corrales F.; Couce M.; Donner M.G.; Ficicioglu C.; Freehauf C.; Frithiof D.; Gotway G.; Hirabayashi K.; Hofstede F.; Hoganson G.; Hwu W.-L.; James P.; Rubio-Gozalbo E.; Scholl-B?rgi S.; Schulze A.; Singh R.; Stabler S.; Stuy M.; Thomas J.; Wagner C.; Wilson W.G.; Wortmann S.; Yamamoto S.; Pao M.; Blom H.J.
臺大學術典藏 2020-12-24T06:16:36Z Mortality, disability, and intensive care in patients with mitochondrial 3243A>G mutation Lee P.-L.; Lu C.-J.; Wang T.-J.; Chu S.-Y.; Lin S.-J.; Hsiue H.-C.; Lee N.-C.; Tsai H.-B.; Yang C.-C.; Wu C.-S.; Lee W.-T.; Weng W.-C.; Fan P.-C.; YIN-HSIU CHIEN; Hwu W.-L.; Hung K.-L.; Huang C.-C.; Chen C.-H.
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.

显示项目 251-260 / 770 (共77页)
<< < 21 22 23 24 25 26 27 28 29 30 > >>
每页显示[10|25|50]项目