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机构 日期 题名 作者
臺大學術典藏 2021-08-23T01:36:01Z High frequency of two mutations in codon 778 in exon 8 of the ATP7B gene in Taiwanese families with Wilson disease Chuang L.-M.; HUEY-PEIR WU; Jang M.-H.; Wang T.-R.; Sue W.-C.; Lin B.J.; Cox D.W.; Tai T.-Y.
臺大學術典藏 2021-07-08T03:25:54Z Bony changes in common mucopolysaccharidoses SHYH-JYE CHEN; Li, Y W; Wang, T R; Hsu, J C
臺大學術典藏 2021-06-29T08:16:07Z Kleine-Levin syndrome in a boy with Prader-Willi syndrome Gau S.-F.; Soong W.-T.; Liu H.-M.; Hou J.-W.; Tsai W.-Y.; YEN-NAN CHIU; Yeh Y.-C.; Wang P.-J.; Wang T.-R.
臺大學術典藏 2021-06-29T08:16:06Z Treatment and outcome of Taiwanese patients with 6-pyruvoyltetrahydropterin synthase gene mutations Chien Y.-H.; Chiang S.-C.; Huang A.; Lin J.-M.; YEN-NAN CHIU; Chou S.-P.; Chu S.-Y.; Wang T.-R.; Hwu W.-L.
臺大學術典藏 2021-06-29T08:16:05Z Phenylalanine hydroxylase deficiency: Intelligence of patients after early dietary treatment Chien Y.-H.; Chiang S.-C.; Huang A.; Lin J.-M.; YEN-NAN CHIU; Chou S.-P.; Wang T.-R.; Hwu W.-L.
臺大學術典藏 2021-06-11T02:56:22Z Trisomy 18 in a patient with CHARGE association. WANG-TSO LEE; Hou J.W.; Yau K.I.; Wang T.R.
臺大學術典藏 2021-06-11T02:54:15Z Duplication of proteolipid protein gene: A possible major cause of Pelizaeus-Merzbacher disease Wang P.-J.; Hwu W.-L.; WANG-TSO LEE; Wang T.-R.; Shen Y.-Z.
臺大學術典藏 2021-06-11T02:54:15Z Cytochrome C oxidase deficiency in fibroblasts of a patient with mitochondrial encephalomyopathy WANG-TSO LEE; Wang P.-J.; Young C.; Wang T.-R.; Shen Y.-Z.
臺大學術典藏 2021-05-26T03:36:28Z Common variable immunodeficiency: An immunological study Tsai K.S.; Chuang C.Y.; Hsieh K.H.; Wang T.R.; KWEN-TAY LUH; Hsu H.C.
臺大學術典藏 2021-05-18T05:54:27Z Author Correction: Hyperpolarization of the subthalamic nucleus alleviates hyperkinetic movement disorders (Scientific Reports, (2020), 10, 1, (8278), 10.1038/s41598-020-65211-w) Tai C.-H.; Pan M.-K.; SHENG-HONG TSENG; Wang T.-R.; Kuo C.-C.

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