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機構	日期	題名	作者
臺大學術典藏	2020-12-16T02:26:29Z	Corrigendum: Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia (Human Molecular Genetics (1995) 4 (1095-1096))	Wuh-Liang Hwu;Chuang S.-C.;Tsai L.-P.;Chang M.-H.;Chang S.-M.;Wang T.-R.; WUH-LIANG HWU; Chuang S.-C.; Tsai L.-P.; Chang M.-H.; Chang S.-M.; Wang T.-R.
臺大學術典藏	2020-12-16T02:26:29Z	Molecular diagnosis of Gaucher disease type II.	Tsai F.J.;Chen H.W.;Peng C.T.;Tsai C.H.;Wuh-Liang Hwu;Wang T.R.;Liu S.C.; Tsai F.J.; Chen H.W.; Peng C.T.; Tsai C.H.; WUH-LIANG HWU; Wang T.R.; Liu S.C.
臺大學術典藏	2020-12-16T02:26:29Z	Fucosidosis in a Chinese girl	WUH-LIANG HWU; Chuang S.C.; Wang W.C.; Wang T.R.
臺大學術典藏	2020-12-16T02:26:29Z	Cytogenetic study of mentally retarded children in Taipei	Wang-Wuu S.; Lai Y.-M.; WUH-LIANG HWU; Wang T.-R.; Wuu K.-D.
臺大學術典藏	2020-12-16T02:26:29Z	Diagnosis of I-cell disease.	WUH-LIANG HWU; Chuang S.C.; Wang W.C.; Wang T.R.
臺大學術典藏	2020-12-16T02:26:28Z	Hepatoblastoma in an infant with Beckwith-Wiedemann Syndrome.	Tsai S.Y.;Jeng Y.M.;Wuh-Liang Hwu;Ni Y.H.;Chang M.H.;Wang T.R.; Tsai S.Y.; Jeng Y.M.; WUH-LIANG HWU; Ni Y.H.; Chang M.H.; Wang T.R.
臺大學術典藏	2020-12-16T02:26:28Z	Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia	Wuh-Liang Hwu;Chuang S.-C.;Tsai L.-P.;Chang M.-H.;Chuang S.-M.;Wang T.-R.; WUH-LIANG HWU; Chuang S.-C.; Tsai L.-P.; Chang M.-H.; Chuang S.-M.; Wang T.-R.
臺大學術典藏	2020-12-16T02:26:28Z	Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type la	Wuh-Liang Hwu;Chuang S.-C.;Tsai L.-P.;Chang M.-H.;Chuang S.-M.;Wang T.-R.; WUH-LIANG HWU; Chuang S.-C.; Tsai L.-P.; Chang M.-H.; Chuang S.-M.; Wang T.-R.
臺大學術典藏	2020-12-16T02:26:28Z	Sex determination in infants with ambiguous genitalia using the polymerase chain reaction of SRY gene.	Tsai F.J.;Tsai C.H.;Wuh-Liang Hwu;Wang T.R.;Shu S.G.;Liu S.C.; Tsai F.J.; Tsai C.H.; WUH-LIANG HWU; Wang T.R.; Shu S.G.; Liu S.C.
臺大學術典藏	2020-12-16T02:26:27Z	FMR1 enhancer is regulated by cAMP through a cAMP-responsive element	Wuh-Liang Hwu; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:27Z	Ornithine transcarbamylase deficiency	Yeh S.-J.;Wuh-Liang Hwu;Tsai W.-S.;Wu T.-J.;Tuchman M.;Wang T.-R.; Yeh S.-J.; WUH-LIANG HWU; Tsai W.-S.; Wu T.-J.; Tuchman M.; Wang T.-R.
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	2020-12-16T02:26:27Z	Diagnosis of mucopolysaccharidosis type IIIB	Wuh-Liang Hwu; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:27Z	Fibroblast growth factor receptor 3 (FGFR3) gene G1138A mutation in Chinese patients with achondroplasia	Wang T.-R.;Wang W.-P.;Wuh-Liang Hwu;Lee M.-L.; Wang T.-R.; Wang W.-P.; WUH-LIANG HWU; Lee M.-L.
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	Human α-L-iduronidase (IDUA) gene: Apparent recombination in intron 2 by haplotype analysis in a Taiwanese population	Lee-Chen G.-J.; Wang T.-R.; WUH-LIANG HWU; Day K.-R.; Wang C.-K.
臺大學術典藏	2020-12-16T02:26:26Z	Mucopolysaccharidosis type II (Hunter's syndrome) in Taiwan	Su P.-H.; WUH-LIANG HWU; Chiang S.-C.; Chiu P.-C.; Lin S.-J.; Shu S.-G.; Wang T.-R.
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	2020-12-16T02:26:26Z	Linkage disequilibrium and linkage analysis of the glucose-6-phosphatase gene	Wong L.-J.C.; Liang M.-H.; WUH-LIANG HWU; Lam C.-W.
臺大學術典藏	2020-12-16T02:26:25Z	Allele distribution at the FMR1 locus in the general Chinese population	Chiang S.-C.;Lee Y.-M.;Wang T.-R.;Wuh-Liang Hwu; Chiang S.-C.; Lee Y.-M.; Wang T.-R.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:25Z	Niemann-Pick disease type C (a cellular cholesterol lipidosis) treated by bone marrow transplantation	Hsu Y.-S.;Wuh-Liang Hwu;Huang S.-F.;Lu M.-Y.;Chen R.-L.;Lin D.-T.;Peng S.S.F.;Lin K.-H.; Hsu Y.-S.; WUH-LIANG HWU; Huang S.-F.; Lu M.-Y.; Chen R.-L.; Lin D.-T.; Peng S.S.F.; Lin K.-H.
臺大學術典藏	2020-12-16T02:26:25Z	Findings of high-resolution chest computed tomography in a young child with Type C Niemann-Pick disease	Peng S.S.-F.; Li Y.-W.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:25Z	Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with apert syndrome	Tsai F.-J.; WUH-LIANG HWU; Lin S.-P.; Chang J.-G.; Wang T.-R.; Tsai C.-H.
臺大學術典藏	2020-12-16T02:26:25Z	Erratum: Molecular genetic study of Pompe disease in Chinese patients in Taiwan (Human Mutation (1999) 13 (380-384))	Ko T.-M.;Wuh-Liang Hwu;Lin Y.-W.;Tseng L.-H.;Hwa H.-L.;Wang T.-R.;Chuang S.- M.;Hayashi K.; Ko T.-M.; WUH-LIANG HWU; Lin Y.-W.; Tseng L.-H.; Hwa H.-L.; Wang T.-R.; Chuang S.- M.; Hayashi K.
臺大學術典藏	2020-12-16T02:26:24Z	3-hydroxy-3-methylglutaric aciduria presenting with Reye like syndrome: Report of one case	Lee C.;Tsai F.-J.;Wu J.-Y.;Peng C.-T.;Tsai C.-H.;Wuh-Liang Hwu;Wang T.-R.;Millington D.S.; Lee C.; Tsai F.-J.; Wu J.-Y.; Peng C.-T.; Tsai C.-H.; WUH-LIANG HWU; Wang T.-R.; Millington D.S.
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	2020-12-16T02:26:23Z	Late-onset holocarboxylase synthetase deficiency with homologous R508W mutation	Wuh-Liang Hwu;Suzuki Y.;Yang X.;Li X.;Chou S.-P.;Narisawa K.;Tsai W.-Y.; WUH-LIANG HWU; Suzuki Y.; Yang X.; Li X.; Chou S.-P.; Narisawa K.; Tsai W.-Y.
臺大學術典藏	2020-12-16T02:26:23Z	Carnitine transport defect presenting with hyperammonemia: Report of one case	Wuh-Liang Hwu;Chiang S.-C.;Chang M.-H.;Wang T.-R.; WUH-LIANG HWU; Chiang S.-C.; Chang M.-H.; Wang T.-R.
臺大學術典藏	2020-12-16T02:26:23Z	Hypercalcaemia in glycogen storage disease type Ia: A case with R83H and 341delG mutations	Wuh-Liang Hwu;Chiang S.-C.;Huang S.-F.;Chang M.-H.;Wen W.-H.;Wang T.-R.; WUH-LIANG HWU; Chiang S.-C.; Huang S.-F.; Chang M.-H.; Wen W.-H.; Wang T.-R.
臺大學術典藏	2020-12-16T02:26:23Z	Glucose-6-phosphatase gene mutations in Taiwan Chinese patients with glycogen storage disease type Ia	Chiang S.-C.;Lee Y.-M.;Chang M.-H.;Wang T.-R.;Ko T.-M.;Wuh-Liang Hwu; Chiang S.-C.; Lee Y.-M.; Chang M.-H.; Wang T.-R.; Ko T.-M.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:22Z	Hereditary fructose intolerance presenting as Reye's-like syndrome: Report of one case	Yang T.-Y.;Chen H.-L.;Ni Y.-H.;Wuh-Liang Hwu;Chang M.-H.; Yang T.-Y.; Chen H.-L.; Ni Y.-H.; WUH-LIANG HWU; Chang M.-H.
臺大學術典藏	2020-12-16T02:26:22Z	Metabolic disorders mimicking Reye's syndrome	Chang P.-F.;Huang S.-F.;Wuh-Liang Hwu;Hou J.-W.;Ni Y.-H.;Chang M.-H.; Chang P.-F.; Huang S.-F.; WUH-LIANG HWU; Hou J.-W.; Ni Y.-H.; Chang M.-H.
臺大學術典藏	2020-12-16T02:26:22Z	Congenital contractural arachnodactyly (Beals syndrome)	Su P.-H.;Hou J.-W.;Wuh-Liang Hwu;Wu M.-H.;Wang J.-K.;Wang T.-R.; Su P.-H.; Hou J.-W.; WUH-LIANG HWU; Wu M.-H.; Wang J.-K.; Wang T.-R.
臺大學術典藏	2020-12-16T02:26:22Z	Identification and characterization of -3c-g acceptor splice site mutation in human α-L-iduronidase associated with mucopolysaccharidosis type IH/S	Teng Y.N.;Wang T.R.;Wuh-Liang Hwu;Lin S.P.;Lee-Chen G.J.; Teng Y.N.; Wang T.R.; WUH-LIANG HWU; Lin S.P.; Lee-Chen G.J.
臺大學術典藏	2020-12-16T02:26:22Z	Dopa-responsive dystonia is induced by a dominant-negative mechanism	Wuh-Liang Hwu;Chiou Y.-W.;Lai S.-Y.;Lee Y.-M.; WUH-LIANG HWU; Chiou Y.-W.; Lai S.-Y.; Lee Y.-M.
臺大學術典藏	2020-12-16T02:26:21Z	MRI in a case of adult-onset citrullinemia	Chen Y.-F.;Huang Y.-C.;Liu H.-M.;Wuh-Liang Hwu; Chen Y.-F.; Huang Y.-C.; Liu H.-M.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:21Z	A Chinese adult onset type II citrullinaemia patient with 851del4/1638ins23 mutations in the SLC25A13 gene.	Wuh-Liang Hwu;Kobayashi K.;Hu Y.H.;Yamaguchi N.;Saheki T.;Chou S.P.;Wang J.H.; WUH-LIANG HWU; Kobayashi K.; Hu Y.H.; Yamaguchi N.; Saheki T.; Chou S.P.; Wang J.H.
臺大學術典藏	2020-12-16T02:26:21Z	Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency	Binzak B.A.;Wevers R.A.;Moolenaar S.H.;Lee Y.-M.;Wuh-Liang Hwu;Poggi-Bach J.;Engelke U.F.H.;Hoard H.M.;Vockley J.G.;Vockley J.; Binzak B.A.; Wevers R.A.; Moolenaar S.H.; Lee Y.-M.; WUH-LIANG HWU; Poggi-Bach J.; Engelke U.F.H.; Hoard H.M.; Vockley J.G.; Vockley J.
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	2020-12-16T02:26:21Z	Molecular genetics of glycogen-storage disease type 1a in Chinese patients of Taiwan	Wong L.-J.C.;Wuh-Liang Hwu;Dai P.;Chen T.-J.; Wong L.-J.C.; WUH-LIANG HWU; Dai P.; Chen T.-J.
臺大學術典藏	2020-12-16T02:26:20Z	Pamidronate treatment of severe osteogenesis imperfecta in a newborn infant	Chien Y.-H.;Chu S.-Y.;Hsu C.-C.;Wuh-Liang Hwu; Chien Y.-H.; Chu S.-Y.; Hsu C.-C.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:20Z	A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients.	Tang N.L.;Wuh-Liang Hwu;Chan R.T.;Law L.K.;Fung L.M.;Zhang W.M.; Tang N.L.; WUH-LIANG HWU; Chan R.T.; Law L.K.; Fung L.M.; Zhang W.M.
臺大學術典藏	2020-12-16T02:26:20Z	Treatment and outcome of Taiwanese patients with 6-pyruvoyltetrahydropterin synthase gene mutations	Chien Y.-H.;Chiang S.-C.;Huang A.;Lin J.-M.;Chiu Y.-N.;Chou S.-P.;Chu S.-Y.;Wang T.-R.;Wuh-Liang Hwu; Chien Y.-H.; Chiang S.-C.; Huang A.; Lin J.-M.; Chiu Y.-N.; Chou S.-P.; Chu S.-Y.; Wang T.-R.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:20Z	Deletion of 11q24.2-qter with agenesis of unilateral internal carotid artery and total anomalous pulmonary venous return [1]	Wu C.-H.;Wuh-Liang Hwu;Wang J.-K.;Young C.;Peng S.S.-F.;Kuo M.-F.; Wu C.-H.; WUH-LIANG HWU; Wang J.-K.; Young C.; Peng S.S.-F.; Kuo M.-F.
臺大學術典藏	2020-12-16T02:26:19Z	Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and Parkin gene mutations	Wu R.-M.;Shan D.-E.;Sun C.-M.;Liu R.-S.;Wuh-Liang Hwu;Tai C.-H.;Hussey J.;West A.;Gwinn-Hardy K.;Hardy J.;Chen J.;Farrer M.;Lincoln S.; Wu R.-M.; Shan D.-E.; Sun C.-M.; Liu R.-S.; WUH-LIANG HWU; Tai C.-H.; Hussey J.; West A.; Gwinn-Hardy K.; Hardy J.; Chen J.; Farrer M.; Lincoln S.
臺大學術典藏	2020-12-16T02:26:19Z	Cockayne syndrome in a family	Chien Y.-H.;Chou H.-C.;Wuh-Liang Hwu; Chien Y.-H.; Chou H.-C.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:19Z	Spontaneous chylothorax in a case of cardio-facio-cutaneous syndrome	Chan P.-C.;Chiu H.-C.;Wuh-Liang Hwu; Chan P.-C.; Chiu H.-C.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:19Z	Cranial MR spectroscopy of tetrahydrobiopterin deficiency	Chien Y.-H.;Peng S.-F.;Wang T.-R.;Wuh-Liang Hwu; Chien Y.-H.; Peng S.-F.; Wang T.-R.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:18Z	An infant with heart murmur and dysmorphic face	Kuo P.-L.; WUH-LIANG HWU; Chien Y.-H.;Kuo P.-L.;Wuh-Liang Hwu; Chien Y.-H.

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