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Showing items 151-175 of 458 (19 Page(s) Totally)
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Institution	Date	Title	Author
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.

Showing items 151-175 of 458 (19 Page(s) Totally)
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