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Institution	Date	Title	Author
臺大學術典藏	2020-12-16T02:26:13Z	RNF4 is a coactivator for nuclear factor Y on GTP cyclohydrolase I proximal promoter	Wu S.-M.;Kuo W.-C.;Wuh-Liang Hwu;Hwa K.-Y.;Mantovani R.;Lee Y.-M.; Wu S.-M.; Kuo W.-C.; WUH-LIANG HWU; Hwa K.-Y.; Mantovani R.; Lee Y.-M.
臺大學術典藏	2020-12-16T02:26:13Z	Gene symbol: WAS. Disease: Wiskott-Aldrich syndrome.	Chien Y.H.;Wuh-Liang Hwu;Ariga T.; Chien Y.H.; WUH-LIANG HWU; Ariga T.
臺大學術典藏	2020-12-16T02:26:12Z	Partial trisomy 1 with congenital hydrocephalus and hypogammaglobulinemia: Report of one case	Wuh-Liang Hwu;Kuo P.-L.;Hung Y.-T.;Chien Y.-H.;Chu S.-Y.; WUH-LIANG HWU; Kuo P.-L.; Hung Y.-T.; Chien Y.-H.; Chu S.-Y.
臺大學術典藏	2020-12-16T02:26:12Z	A step-wise diagnosis of fragile X syndrome in Taiwan	Huang Y.-T.;Chiang S.-C.;Tzeng C.-C.;Liu C.-H.;Chien Y.-H.;Wuh-Liang Hwu; Huang Y.-T.; Chiang S.-C.; Tzeng C.-C.; Liu C.-H.; Chien Y.-H.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:12Z	Detection of a homozygous D645E mutation of the acid α-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II [3]	Chen C.-P.;Lin S.-P.;Tzen C.-Y.;Tsai F.-J.;Wuh-Liang Hwu;Wang W.; Chen C.-P.; Lin S.-P.; Tzen C.-Y.; Tsai F.-J.; WUH-LIANG HWU; Wang W.
臺大學術典藏	2020-12-16T02:26:12Z	Distal Arthrogryposis in Two Sisters Born to Different Fathers [4]	Wuh-Liang Hwu;Chien Y.-H.;Hsu C.-C.; WUH-LIANG HWU; Chien Y.-H.; Hsu C.-C.
臺大學術典藏	2020-12-16T02:26:11Z	Carbohydrate deficient glycoprotein syndrome type IA	Chu K.-L.;Chien Y.-H.;Tsai C.-E.;Freeze H.H.;Eklund E.;Wuh-Liang Hwu; Chu K.-L.; Chien Y.-H.; Tsai C.-E.; Freeze H.H.; Eklund E.; 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	2020-12-16T02:26:11Z	Molecular chaperones affect GTP cyclohydrolase I mutations in dopa-responsive dystonia	Wuh-Liang Hwu;Lu M.-Y.;Hwa K.-Y.;Fan S.-W.;Lee Y.-M.; WUH-LIANG HWU; Lu M.-Y.; Hwa K.-Y.; Fan S.-W.; Lee Y.-M.
臺大學術典藏	2020-12-16T02:26:11Z	Trisomy 18 in monozygotic twins with discordant phenotypes	Lee J.-T.;Chou H.-C.;Tsao P.-N.;Hsieh W.-S.;Wuh-Liang Hwu; Lee J.-T.; Chou H.-C.; Tsao P.-N.; Hsieh W.-S.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:11Z	Terminal deletion of chromosome 2q associated with Graves' disease: A case report and literature review	Chu S.-Y.;Tsai W.-Y.;Chien Y.-H.;Fang J.-S.;Ku C.-W.;Chang P.-Y.;Wuh-Liang Hwu; Chu S.-Y.; Tsai W.-Y.; Chien Y.-H.; Fang J.-S.; Ku C.-W.; Chang P.-Y.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:10Z	DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients	Wang C.K.;Wu Y.R.;Wuh-Liang Hwu;Chen C.M.;Ro L.S.;Chen S.T.;Gwinn-Hardy K.;Yang C.C.;Wu R.M.;Chen T.F.;Wang H.C.;Chao M.C.;Chiu M.J.;Lu C.J.;Lee-Chen G.J.; Wang C.K.; Wu Y.R.; WUH-LIANG HWU; Chen C.M.; Ro L.S.; Chen S.T.; Gwinn-Hardy K.; Yang C.C.; Wu R.M.; Chen T.F.; Wang H.C.; Chao M.C.; Chiu M.J.; Lu C.J.; Lee-Chen G.J.
臺大學術典藏	2020-12-16T02:26:10Z	Diffusion tensor images in children with early-treated, chronic, malignant phenylketonuric: Correlation with intelligence assessment	Chien Y.-H.; WUH-LIANG HWU; Liu H.-M.; Peng S.S.-F.;Tseng W.-Y.I.;Chien Y.-H.;Wuh-Liang Hwu;Liu H.-M.; Peng S.S.-F.; Tseng W.-Y.I.
臺大學術典藏	2020-12-16T02:26:10Z	Molecular diagnosis of Wiskott-Aldrich syndrome in Taiwan	Chien Y.-H.;Wuh-Liang Hwu;Ariga T.;Chang K.-W.;Yang Y.-H.;Lin K.-H.;Chiang B.-L.; Chien Y.-H.; WUH-LIANG HWU; Ariga T.; Chang K.-W.; Yang Y.-H.; Lin K.-H.; Chiang B.-L.
臺大學術典藏	2020-12-16T02:26:09Z	Plasma chitotriosidase activity and malaria (multiple letters)	Chien Y.-H.;Chen J.-H.;Wuh-Liang Hwu;Musumeci S.; Chien Y.-H.; Chen J.-H.; WUH-LIANG HWU; Musumeci S.
臺大學術典藏	2020-12-16T02:26:09Z	Fundus abnormalities in a patient with type I Gaucher's disease with 12-year follow-up	Wang T.-J.;Chen M.-S.;Shih Y.-F.;Wuh-Liang Hwu;Lai M.-Y.; Wang T.-J.; Chen M.-S.; Shih Y.-F.; WUH-LIANG HWU; Lai M.-Y.
臺大學術典藏	2020-12-16T02:26:09Z	Parkin mutations and early-onset parkinsonism in a Taiwanese cohort	Wu R.-M.;Bounds R.;Lincoln S.;Hulihan M.;Lin C.-H.;Wuh-Liang Hwu;Chen J.;Gwinn-Hardy K.;Farrer M.; Wu R.-M.; Bounds R.; Lincoln S.; Hulihan M.; Lin C.-H.; WUH-LIANG HWU; Chen J.; Gwinn-Hardy K.; Farrer M.
臺大學術典藏	2020-12-16T02:26:09Z	Phenylalanine hydroxylase deficiency: Intelligence of patients after early dietary treatment	Chien Y.-H.;Chiang S.-C.;Huang A.;Lin J.-M.;Chiu Y.-N.;Chou S.-P.;Wang T.-R.;Wuh-Liang Hwu; Chien Y.-H.; Chiang S.-C.; Huang A.; Lin J.-M.; Chiu Y.-N.; Chou S.-P.; Wang T.-R.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:08Z	KIF21A gene c.2860C>T mutation in congenital fibrosis of extraocular muscles type 1 and 3	Lin L.-K.;Chien Y.-H.;Wu J.-Y.;Wang A.-H.;Chiang S.-C.;Wuh-Liang Hwu; Lin L.-K.; Chien Y.-H.; Wu J.-Y.; Wang A.-H.; Chiang S.-C.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:08Z	Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C	Yang C.-C.;Su Y.-N.;Chiou P.-C.;Fietz M.J.;Yu C.-L.;Wuh-Liang Hwu;Lee M.-J.; Yang C.-C.; Su Y.-N.; Chiou P.-C.; Fietz M.J.; Yu C.-L.; WUH-LIANG HWU; Lee M.-J.
臺大學術典藏	2020-12-16T02:26:08Z	Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype	Tzeng C.-C.;Tsai L.-P.;Wuh-Liang Hwu;Lin S.-J.;Chao M.-C.;Jong Y.-J.;Chu S.-Y.;Chao W.-C.;Lu C.-L.; Tzeng C.-C.; Tsai L.-P.; WUH-LIANG HWU; Lin S.-J.; Chao M.-C.; Jong Y.-J.; Chu S.-Y.; Chao W.-C.; Lu C.-L.
臺大學術典藏	2020-12-16T02:26:08Z	Mapping of psoriasis to 17q terminus	Wuh-Liang Hwu;Yang C.-F.;Fann C.S.J.;Chen C.-L.;Tsai T.-F.;Chein Y.-H.;Chiang S.-C.;Chen C.-H.;Hung S.-I.;Wu J.-Y.;Chen Y.-T.; WUH-LIANG HWU; Yang C.-F.; Fann C.S.J.; Chen C.-L.; Tsai T.-F.; Chein Y.-H.; Chiang S.-C.; Chen C.-H.; Hung S.-I.; Wu J.-Y.; Chen Y.-T.
臺大學術典藏	2020-12-16T02:26:07Z	Viral infections and prolonged fever after liver transplantation in young children with inborn errors of metabolism	Huang H.-P.;Chien Y.-H.;Huang L.-M.;Ni Y.-H.;Chang M.-H.;Ho M.-C.;Lee P.-H.;Wuh-Liang Hwu; Huang H.-P.; Chien Y.-H.; Huang L.-M.; Ni Y.-H.; Chang M.-H.; Ho M.-C.; Lee P.-H.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:07Z	Type I Gaucher disease with exophthalmos and pulmonary arteriovenous malformation	Chen C.-A.;Tang N.L.S.;Chen Y.-H.;Zhang W.-M.;Wang J.-K.;Wuh-Liang Hwu; Chen C.-A.; Tang N.L.S.; Chen Y.-H.; Zhang W.-M.; Wang J.-K.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:07Z	Spectrum of hypermethioninemia in neonatal screening	Chien Y.-H.;Chiang S.-C.;Huang A.;Wuh-Liang Hwu; Chien Y.-H.; Chiang S.-C.; Huang A.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:07Z	Reye's syndrome developing in an infant on treatment of Kawasaki syndrome	Wei C.-M.;Chen H.-L.;Lee P.-I.;Chen C.-M.;Ma C.-Y.;Wuh-Liang Hwu; Wei C.-M.; Chen H.-L.; Lee P.-I.; Chen C.-M.; Ma C.-Y.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:06Z	Tandem mass neonatal screening in Taiwan - Report from one center	Huang H.-P.;Chu K.-L.;Chien Y.-H.;Wei M.-L.;Wu S.-T.;Wang S.-F.;Wuh-Liang Hwu; Huang H.-P.; Chu K.-L.; Chien Y.-H.; Wei M.-L.; Wu S.-T.; Wang S.-F.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:06Z	Homozygous SLC25A13 mutation in a Taiwanese patient with adult-onset citrullinemia complicated with steatosis and hepatocellular carcinoma	Tsai C.-W.;Yang C.-C.;Chen H.-L.;Wuh-Liang Hwu;Wu M.-Z.;Liu K.-L.;Wu M.-S.; Tsai C.-W.; Yang C.-C.; Chen H.-L.; WUH-LIANG HWU; Wu M.-Z.; Liu K.-L.; Wu M.-S.
臺大學術典藏	2020-12-16T02:26:06Z	Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1.	Lee M.J.;Su Y.N.;You H.L.;Chiou S.C.;Lin L.C.;Yang C.C.;Lee W.C.;Wuh-Liang Hwu;Hsieh F.J.;Stephenson D.A.;Yu C.L.; Lee M.J.; Su Y.N.; You H.L.; Chiou S.C.; Lin L.C.; Yang C.C.; Lee W.C.; WUH-LIANG HWU; Hsieh F.J.; Stephenson D.A.; Yu C.L.
臺大學術典藏	2020-12-16T02:26:06Z	Adenoviral interneuronal transportation after retrograde gene transfer in mice	Tsai L.-K.;Tsai M.-S.;Shyue S.-K.;Wuh-Liang Hwu;Li H.; Tsai L.-K.; Tsai M.-S.; Shyue S.-K.; WUH-LIANG HWU; Li H.
臺大學術典藏	2020-12-16T02:26:05Z	Hepatic steatosis and neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) in Taiwanese infants	Yeh J.-N.;Jeng Y.-M.;Chen H.-L.;Ni Y.-H.;Wuh-Liang Hwu;Chang M.-H.; Yeh J.-N.; Jeng Y.-M.; Chen H.-L.; Ni Y.-H.; WUH-LIANG HWU; Chang M.-H.
臺大學術典藏	2020-12-16T02:26:05Z	A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease	Kishnani P.S.;Wuh-Liang Hwu;Mandel H.;Nicolino M.;Yong F.;Corzo D.; Kishnani P.S.; WUH-LIANG HWU; Mandel H.; Nicolino M.; Yong F.; Corzo D.
臺大學術典藏	2020-12-16T02:26:04Z	Brain development in infantile-onset pompe disease treated by enzyme replacement therapy	Chien Y.-H.;Lee N.-C.;Peng S.-F.;Wuh-Liang Hwu; Chien Y.-H.; Lee N.-C.; Peng S.-F.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:04Z	Time course of acylcarnitine elevation in neonatal intrahepatic cholestasis caused by citrin deficiency	Lee N.-C.;Chien Y.-H.;Kobayashi K.;Saheki T.;Chen H.-L.;Chiu P.-C.;Ni Y.-H.;Chang M.-H.;Wuh-Liang Hwu; Lee N.-C.; Chien Y.-H.; Kobayashi K.; Saheki T.; Chen H.-L.; Chiu P.-C.; Ni Y.-H.; Chang M.-H.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:04Z	Mutation analysis of Gaucher disease patients in Taiwan: High prevalence of the RecNciI and L444P mutations	Wan L.;Hsu C.-M.;Tsai C.-H.;Lee C.-C.;Wuh-Liang Hwu;Tsai F.-J.; Wan L.; Hsu C.-M.; Tsai C.-H.; Lee C.-C.; WUH-LIANG HWU; Tsai F.-J.
臺大學術典藏	2020-12-16T02:26:03Z	Identification and management of cardiac perforation from a double lumen catheter in an infant [6]	Wang C.-C.;Chen Y.-W.;Wu E.-T.;Chien Y.-H.;Wuh-Liang Hwu;Ko W.-J.;Huang S.-C.; Wang C.-C.; Chen Y.-W.; Wu E.-T.; Chien Y.-H.; WUH-LIANG HWU; Ko W.-J.; Huang S.-C.
臺大學術典藏	2020-12-16T02:26:03Z	Recombinant human acid α-glucosidase: Major clinical benefits in infantile-onset Pompe disease	Kishnani P.S.;Corzo D.;Nicolino M.;Byrne B.;Mandel H.;Wuh-Liang Hwu;Leslie N.;Levine J.;Spencer C.;Mcdonald M.;Li J.;Dumontier J.;Halberthal M.;Chien Y.H.;Hopkin R.;Vijayaraghavan S.;Gruskin D.;Bartholomew D.;Van Der Ploeg A.;Clancy J.P.;Parini R.;Morin G.;Beck M.;De La Gastine G.S.;Jokic M.;Thurberg B.;Richards S.;Bali D.;Davison M.;Worden M.A.;Chen Y.T.;Wraith J.E.; Kishnani P.S.; Corzo D.; Nicolino M.; Byrne B.; Mandel H.; WUH-LIANG HWU; Leslie N.; Levine J.; Spencer C.; McDonald M.; Li J.; Dumontier J.; Halberthal M.; Chien Y.H.; Hopkin R.; Vijayaraghavan S.; Gruskin D.; Bartholomew D.; Van Der Ploeg A.; Clancy J.P.; Parini R.; Morin G.; Beck M.; De La Gastine G.S.; Jokic M.; Thurberg B.; Richards S.; Bali D.; Davison M.; Worden M.A.; Chen Y.T.; Wraith J.E.
臺大學術典藏	2020-12-16T02:26:03Z	Establishing a standardized therapeutic testing protocol for spinal muscular atrophy	Tsai L.-K.;Tsai M.-S.;Lin T.-B.;Wuh-Liang Hwu;Li H.; Tsai L.-K.; Tsai M.-S.; Lin T.-B.; WUH-LIANG HWU; Li H.
臺大學術典藏	2020-12-16T02:26:03Z	Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype	Chen M.;Wuh-Liang Hwu;Kuo S.-J.;Chen C.-P.;Yin P.-L.;Chang S.-P.;Lee D.-J.;Chen T.-H.;Wang B.-T.;Lin C.-C.; Chen M.; WUH-LIANG HWU; Kuo S.-J.; Chen C.-P.; Yin P.-L.; Chang S.-P.; Lee D.-J.; Chen T.-H.; Wang B.-T.; Lin C.-C.
臺大學術典藏	2020-12-16T02:26:02Z	Slipped capital femoral epiphysis as a complication of growth hormone therapy.	Wang S.Y.;Tung Y.C.;Tsai W.Y.;Chien Y.H.;Lee J.S.;Wuh-Liang Hwu; Wang S.Y.; Tung Y.C.; Tsai W.Y.; Chien Y.H.; Lee J.S.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:02Z	Treatment of Niemann-Pick disease type C in two children with miglustat: initial responses and maintenance of effects over 1 year.	Chien Y.H.;Lee N.C.;Tsai L.K.;Huang A.C.;Peng S.F.;Chen S.J.;Wuh-Liang Hwu; Chien Y.H.; Lee N.C.; Tsai L.K.; Huang A.C.; Peng S.F.; Chen S.J.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:01Z	Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome)	Chen C.-P.;Lin S.-P.;Tzen C.-Y.;Wuh-Liang Hwu;Chern S.-R.;Chuang C.-K.;Chiang S.-S.;Wang W.; Chen C.-P.; Lin S.-P.; Tzen C.-Y.; WUH-LIANG HWU; Chern S.-R.; Chuang C.-K.; Chiang S.-S.; Wang W.
臺大學術典藏	2020-12-16T02:26:01Z	Copy number analysis of survival motor neuron genes by multiplex ligation-dependent probe amplification	Huang C.-H.;Chang Y.-Y.;Chen C.-H.;Kuo Y.-S.;Wuh-Liang Hwu;Gerdes T.;Ko T.-M.; Huang C.-H.; Chang Y.-Y.; Chen C.-H.; Kuo Y.-S.; WUH-LIANG HWU; Gerdes T.; Ko T.-M.
臺大學術典藏	2020-12-16T02:26:01Z	Deficiency of the carnitine transporter (OCTN2) with partial N-acetylglutamate synthase (NAGS) deficiency.	Wuh-Liang Hwu;Chien Y.H.;Tang N.L.;Law L.K.;Lin C.Y.;Lee N.C.; WUH-LIANG HWU; Chien Y.H.; Tang N.L.; Law L.K.; Lin C.Y.; Lee N.C.
臺大學術典藏	2020-12-16T02:26:01Z	Human gene mutations. Gene symbol: GLA. Disease: Fabry disease.	Lin W.D.;Wuh-Liang Hwu;Liu S.C.;Chen C.P.;Tsai F.J.; Lin W.D.; WUH-LIANG HWU; Liu S.C.; Chen C.P.; Tsai F.J.
臺大學術典藏	2020-12-16T02:26:00Z	Newborn screening for pompe disease: Synthesis of the evidence and development of screening recommendations	Kemper A.R.;Wuh-Liang Hwu;Lloyd-Puryear M.;Kishnani P.S.; Kemper A.R.; WUH-LIANG HWU; Lloyd-Puryear M.; Kishnani P.S.
臺大學術典藏	2020-12-16T02:26:00Z	Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (Ethnic Chinese) cohort of familial and early-onset parkinsonism	Lin C.-H.;Wuh-Liang Hwu;Chiang S.-C.;Tai C.-H.;Wu R.-M.; Lin C.-H.; WUH-LIANG HWU; Chiang S.-C.; Tai C.-H.; Wu R.-M.
臺大學術典藏	2020-12-16T02:26:00Z	Outcome of pulmonary and aortic stenosis in Williams-Beuren syndrome in an Asian cohort	Wu E.-T.; Lu F.; Wang J.-K.; Wu M.-H.; Wang C.-C.;Wuh-Liang Hwu;Wu E.-T.;Lu F.;Wang J.-K.;Wu M.-H.; Wang C.-C.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:00Z	The design and implementation of a next generation information system for newborn screening	Tu C.-M.;Tang M.-Y.;Chang H.-Y.;Wuh-Liang Hwu;Chien Y.-H.;Lai F.; Tu C.-M.; Tang M.-Y.; Chang H.-Y.; WUH-LIANG HWU; Chien Y.-H.; Lai F.
臺大學術典藏	2020-12-16T02:25:59Z	A promoter sequence variant of ZNF750 is linked with familial psoriasis	Yang C.-F.;Wuh-Liang Hwu;Yang L.-C.;Chung W.-H.;Chien Y.-H.;Hung C.-F.;Chen H.-C.;Tsai P.-J.;Fann C.S.J.;Liao F.;Chen Y.-T.; Yang C.-F.; WUH-LIANG HWU; Yang L.-C.; Chung W.-H.; Chien Y.-H.; Hung C.-F.; Chen H.-C.; Tsai P.-J.; Fann C.S.J.; Liao F.; Chen Y.-T.

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