臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Institution	Date	Title	Author
臺大學術典藏	2020-09-22T09:06:23Z	Niemann-Pick disease type C (a cellular cholesterol lipidosis) treated by bone marrow transplantation	Hsu Y.-S.;Hwu W.-L.;Huang S.-F.;Lu M.-Y.;Chen R.-L.;Lin D.-T.;Steven Shinn-Forng Peng;Lin K.-H.; Hsu Y.-S.; Hwu W.-L.; Huang S.-F.; Lu M.-Y.; Chen R.-L.; Lin D.-T.; STEVEN SHINN-FORNG PENG; Lin K.-H.
臺大學術典藏	2020-09-22T09:06:19Z	Cranial MR spectroscopy of tetrahydrobiopterin deficiency	Hwu W.-L.; Wang T.-R.; STEVEN SHINN-FORNG PENG; Chien Y.-H.; Chien Y.-H.;Steven Shinn-Forng Peng;Wang T.-R.;Hwu W.-L.
臺大學術典藏	2020-09-22T09:06:16Z	Diffusion tensor images in children with early-treated, chronic, malignant phenylketonuric: Correlation with intelligence assessment	Steven Shinn-Forng Peng;Tseng W.-Y.I.;Chien Y.-H.;Hwu W.-L.;Liu H.-M.; STEVEN SHINN-FORNG PENG; Tseng W.-Y.I.; Chien Y.-H.; Hwu W.-L.; Liu H.-M.
臺大學術典藏	2020-09-22T09:06:16Z	Adrenoleukodystrophy: Clinical analysis of 9 Taiwanese children	Liang J.-S.;Lee W.-T.;Hwu W.-L.;Steven Shinn-Forng Peng;Chu L.-W.;Wang P.-J.;Shen Y.-Z.; Liang J.-S.; Lee W.-T.; Hwu W.-L.; STEVEN SHINN-FORNG PENG; Chu L.-W.; Wang P.-J.; Shen Y.-Z.
臺大學術典藏	2020-09-22T09:06:13Z	Brain development in infantile-onset pompe disease treated by enzyme replacement therapy	Chien Y.-H.;Lee N.-C.;Steven Shinn-Forng Peng;Hwu W.-L.; Chien Y.-H.; Lee N.-C.; STEVEN SHINN-FORNG PENG; Hwu W.-L.
臺大學術典藏	2020-09-22T09:06:12Z	Treatment of Niemann-Pick disease type C in two children with miglustat: initial responses and maintenance of effects over 1 year.	Chen S.J.; Hwu W.L.; STEVEN SHINN-FORNG PENG; Huang A.C.; Tsai L.K.; Lee N.C.; Chien Y.H.; Chien Y.H.;Lee N.C.;Tsai L.K.;Huang A.C.;Steven Shinn-Forng Peng;Chen S.J.;Hwu W.L.
臺大學術典藏	2020-09-22T09:06:11Z	Brain Damage by Mild Metabolic Derangements in Methylmalonic Acidemia	Hwu W.-L.; Tseng S.-C.; Hsu L.-W.; Wu A.S.-H.; Chen L.-C.; Huang A.-C.; Liu T.-T.; STEVEN SHINN-FORNG PENG; Lee N.-C.; Chien Y.-H.
臺大學術典藏	2020-09-22T09:06:10Z	Schizencephaly in LEOPARD Syndrome	STEVEN SHINN-FORNG PENG; Liang J.-S.;Chien Y.-H.;Hwu W.-L.;Yeh S.-J.;Steven Shinn-Forng Peng; Liang J.-S.; Chien Y.-H.; Hwu W.-L.; Yeh S.-J.
臺大學術典藏	2020-09-22T09:06:08Z	Congenital hypopituitarism due to POU1F1 gene mutation	Lee N.-C.;Tsai W.-Y.;Steven Shinn-Forng Peng;Tung Y.-C.;Chien Y.-H.;Hwu W.-L.; Lee N.-C.; Tsai W.-Y.; STEVEN SHINN-FORNG PENG; Tung Y.-C.; Chien Y.-H.; Hwu W.-L.
臺大學術典藏	2020-09-22T09:06:06Z	A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a child	STEVEN SHINN-FORNG PENG; Weng W.-C.; Liu H.-M.; Tsai L.-P.; Chien Y.-H.; Wu J.-F.; Wu E.-T.; Huang P.-H.; Lee W.-T.; Tsai I.-J.; Hwu W.-L.; Lee N.-C.

Showing items 491-500 of 770 (77 Page(s) Totally)
<< < 45 46 47 48 49 50 51 52 53 54 > >>
View [10|25|50] records per page