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Showing items 36-60 of 139 (6 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2021-01-05T08:08:15Z	Kabuki make-up syndrome associated with congenital heart disease.	Wang P.J.; Chiu I.S.; Wang L.C.; MEI-HWAN WU; Wang J.K.; Hung Y.B.; Lin S.J.
臺大學術典藏	2020-12-24T06:17:20Z	Adrenoleukodystrophy initially diagnosed as idiopathic Addison's disease in two patients: The importance of early testing	Hwu W.-L.; YIN-HSIU CHIEN; Liang J.-S.; Lee W.-T.; Wang P.-J.; Tsai W.-Y.
臺大學術典藏	2020-12-24T06:16:15Z	Early initiation of high-dose oral ambroxol in combination with enzyme replacement therapy in a neuropathic Gaucher infant	YIN-HSIU CHIEN; Wang P.-J.; Chien C.-C.; Hwu W.-L.; Chu S.-Y.
臺大學術典藏	2020-12-22T03:29:59Z	Nonprogressive congenital unilateral ventriculomegaly	Po-Nien Tsao;Teng R.-J.;Wu T.-J.;Yau K.-I.T.;Wang P.-J.; PO-NIEN TSAO; Teng R.-J.; Wu T.-J.; Yau K.-I.T.; Wang P.-J.
臺大學術典藏	2020-12-21T01:58:28Z	Severe myoclonic epilepsy in infancy: evolution of electroencephalographic and clinical features.	Shen Y.Z.; Huang C.C.; Young C.; Lee W.T.; PI-CHUAN FAN; Wang P.J.; Wang P.J.;Pi-Chuan Fan;Lee W.T.;Young C.;Huang C.C.;Shen Y.Z.
臺大學術典藏	2020-12-18T02:21:59Z	Adrenoleukodystrophy initially diagnosed as idiopathic Addison's disease in two patients: The importance of early testing	Tsai W.-Y.; Wang P.-J.; WANG-TSO LEE; Liang J.-S.; Chien Y.-H.; Hwu W.-L.; Hwu W.-L.;Chien Y.-H.;Liang J.-S.;Wang-Tso Lee;Wang P.-J.;Tsai W.-Y.
臺大學術典藏	2020-12-18T02:21:58Z	The roles of electroencephalography and neuroimaging in children with holoprosencephaly	Shen Y.-Z.; Wang P.-J.; Liang J.-S.; Tseng C.-L.; Lin H.-C.; Peng S.S.; WANG-TSO LEE; Yang M.-T.; Yang M.-T.;Wang-Tso Lee;Peng S.S.;Lin H.-C.;Tseng C.-L.;Liang J.-S.;Wang P.-J.;Shen Y.-Z.
臺大學術典藏	2020-12-18T02:21:58Z	Adrenoleukodystrophy: Clinical analysis of 9 Taiwanese children	Liang J.-S.;Wang-Tso Lee;Hwu W.-L.;Peng S.S.-F.;Chu L.-W.;Wang P.-J.;Shen Y.-Z.; Liang J.-S.; WANG-TSO LEE; Hwu W.-L.; Peng S.S.-F.; Chu L.-W.; Wang P.-J.; Shen Y.-Z.
臺大學術典藏	2020-12-18T02:21:57Z	Electroclinical characteristics of seizures - Comparing Prader-Willi syndrome with Angelman syndrome	Wang P.-J.;Hou J.-W.;Sue W.-C.;Wang-Tso Lee; Wang P.-J.; Hou J.-W.; Sue W.-C.; WANG-TSO LEE
臺大學術典藏	2020-12-18T02:21:55Z	ACTH therapy for Taiwanese children with West syndrome - Efficacy and impact on long-term prognosis	WANG-TSO LEE; Shen Y.-Z.; Wang P.-J.; Young C.; Lin H.-C.
臺大學術典藏	2020-12-16T02:26:33Z	Hereditary progressive dystonia with marked diurnal fluctuation: report of a case.	WUH-LIANG HWU; Wang P.J.; Shen Y.Z.
臺大學術典藏	2020-12-16T02:26:32Z	Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case.	Wuh-Liang Hwu;Tsai W.Y.;Lee J.S.;Wang P.J.;Wang T.R.; WUH-LIANG HWU; Tsai W.Y.; Lee J.S.; Wang P.J.; Wang T.R.
臺大學術典藏	2020-12-16T02:26:30Z	Hereditary progressive dystonia with marked diurnal fluctuation (Segawa syndrome) in Taiwan	Wang P.-J.; Ko Y.-M.; Young C.; WUH-LIANG HWU; Shen Y.-Z.
臺大學術典藏	2020-12-16T02:26:27Z	Arylsulfatase A pseudodeficiency in Chinese	Wuh-Liang Hwu;Tsai L.-P.;Wang W.-C.;Chuang S.-C.;Wang P.-J.;Wang T.-R.; WUH-LIANG HWU; Tsai L.-P.; Wang W.-C.; Chuang S.-C.; Wang P.-J.; Wang T.-R.
臺大學術典藏	2020-12-16T02:26:26Z	The controversy regarding diagnostic criteria for early myoclonic encephalopathy	Wang P.-J.; Lee W.-T.; WUH-LIANG HWU; Young C.; Yau K.-I.T.; Shen Y.-Z.
臺大學術典藏	2020-12-16T02:26:26Z	Duplication of proteolipid protein gene: A possible major cause of Pelizaeus-Merzbacher disease	Wang P.-J.;Wuh-Liang Hwu;Lee W.-T.;Wang T.-R.;Shen Y.-Z.; Wang P.-J.; WUH-LIANG HWU; Lee W.-T.; Wang T.-R.; Shen Y.-Z.
臺大學術典藏	2020-12-16T02:26:24Z	Dopa-responsive dystonia induced by a recessive GTP cyclohydrolase I mutation	Wuh-Liang Hwu;Wang P.-J.;Hsiao K.-J.;Wang T.-R.;Chiou Y.-W.;Lee Y.-M.; WUH-LIANG HWU; Wang P.-J.; Hsiao K.-J.; Wang T.-R.; Chiou Y.-W.; Lee Y.-M.
臺大學術典藏	2020-12-16T02:26:24Z	Neonatal type of nonketotic hyperglycinemia	Lu F.L.;Wang P.-J.;Wuh-Liang Hwu;Tsou Yau K.-I.;Wang T.-R.; Lu F.L.; Wang P.-J.; WUH-LIANG HWU; Tsou Yau K.-I.; Wang T.-R.
臺大學術典藏	2020-12-16T02:26:21Z	Epileptic seizures and electroencephalographic evolution in genetic leukodystrophies	Wang P.-J.;Wuh-Liang Hwu;Shen Y.-Z.; Wang P.-J.; WUH-LIANG HWU; Shen Y.-Z.
臺大學術典藏	2020-12-16T02:26:16Z	Adrenoleukodystrophy initially diagnosed as idiopathic Addison's disease in two patients: The importance of early testing	Wuh-Liang Hwu;Chien Y.-H.;Liang J.-S.;Lee W.-T.;Wang P.-J.;Tsai W.-Y.; WUH-LIANG HWU; Chien Y.-H.; Liang J.-S.; Lee W.-T.; Wang P.-J.; Tsai W.-Y.
臺大學術典藏	2020-12-16T02:26:15Z	Maple Syrup Urine Disease Presenting with Neonatal Status Epilepticus: Report of One Case	Wang I.-J.;Chu S.-Y.;Wang C.-Y.;Wang P.-J.;Wuh-Liang Hwu; Wang I.-J.; Chu S.-Y.; Wang C.-Y.; Wang P.-J.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:11Z	Adrenoleukodystrophy: Clinical analysis of 9 Taiwanese children	Liang J.-S.;Lee W.-T.;Wuh-Liang Hwu;Peng S.S.-F.;Chu L.-W.;Wang P.-J.;Shen Y.-Z.; Liang J.-S.; Lee W.-T.; WUH-LIANG HWU; Peng S.S.-F.; Chu L.-W.; Wang P.-J.; Shen Y.-Z.
臺大學術典藏	2020-12-16T02:24:59Z	Early initiation of high-dose oral ambroxol in combination with enzyme replacement therapy in a neuropathic Gaucher infant	Chu S.-Y.;Chien C.-C.;Wuh-Liang Hwu;Wang P.-J.;Chien Y.-H.; Chu S.-Y.; Chien C.-C.; WUH-LIANG HWU; Wang P.-J.; Chien Y.-H.
臺大學術典藏	2020-12-09T05:58:48Z	Neonatal type of nonketotic hyperglycinemia	Frank Leigh Lu;Wang P.-J.;Hwu W.-L.;Tsou Yau K.-I.;Wang T.-R.; FRANK LEIGH LU; Wang P.-J.; Hwu W.-L.; Tsou Yau K.-I.; Wang T.-R.
臺大學術典藏	2020-11-03T11:20:46Z	Estimation of prevalence and incidence of infantile spasms in Taiwan using capture-recapture method	Chen C.-C.; TA-FU CHEN; Lin H.-C.; Oon P.-C.; Wu H.-M.; Wang P.-J.; Chen T.H.-H.; Liou H.-H.; Chen C.-C.;Ta-Fu Chen;Lin H.-C.;Oon P.-C.;Wu H.-M.;Wang P.-J.;Chen T.H.-H.;Liou H.-H.

Showing items 36-60 of 139 (6 Page(s) Totally)
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