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機構 日期 題名 作者
臺大學術典藏 2020-12-16T02:25:11Z Performance of the four-plex tandem mass spectrometry lysosomal storage disease newborn screening test: The necessity of adding a 2nd tier test for Pompe disease Chiang S.-C.;Chen P.-W.;Wuh-Liang Hwu;Lee A.-J.;Chen L.-C.;Lee N.-C.;Chiou L.-Y.;Chien Y.-H.; Chiang S.-C.; Chen P.-W.; WUH-LIANG HWU; Lee A.-J.; Chen L.-C.; Lee N.-C.; Chiou L.-Y.; Chien Y.-H.
臺大學術典藏 2020-12-16T02:25:10Z Functional independence of Taiwanese patients with mucopolysaccharidoses Lee C.-L.;Lin H.-Y.;Chuang C.-K.;Chiu H.-C.;Tu R.-Y.;Huang Y.-H.;Wuh-Liang Hwu;Tsai F.-J.;Chiu P.-C.;Niu D.-M.;Chen Y.-J.;Chao M.-C.;Chang T.-M.;Lin J.-L.;Chang C.-Y.;Kao Y.-C.;Lin S.-P.; Lee C.-L.; Lin H.-Y.; Chuang C.-K.; Chiu H.-C.; Tu R.-Y.; Huang Y.-H.; WUH-LIANG HWU; Tsai F.-J.; Chiu P.-C.; Niu D.-M.; Chen Y.-J.; Chao M.-C.; Chang T.-M.; Lin J.-L.; Chang C.-Y.; Kao Y.-C.; Lin S.-P.
臺大學術典藏 2020-12-16T02:25:10Z Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders—A successful strategy for clinical research of rare diseases Posset R.;Garbade S.F.;Boy N.;Burlina A.B.;Dionisi-Vici C.;Dobbelaere D.;Garcia-Cazorla A.;De Lonlay P.;Teles E.L.;Vara R.;Mew N.A.;Batshaw M.L.;Baumgartner M.R.;Mccandless S.E.;Seminara J.;Summar M.;Hoffmann G.F.;K?Lker S.;Burgard P.;Berry S.A.;Burrage L.;Coughlin C.;Diaz G.A.;Gallagher R.C.;Gropman A.;Harding C.O.;Lee B.;Le Mons C.;Lawrence Merritt J.;Ii, Nagamani S.C.S.;Schulze A.;Stricker T.;Tuchman M.;Waisbren S.;Weisfeldadams J.;Wong D.;Yudkoff M.;Arnoux J.;BariĆI.;Bosch A.M.;Chabrol B.;Chakrapani A.;Cort?Ssaladefont E.;Couce M.L.;Eyskens F.;De Laet C.;De Meirleir L.;Freisinger P.;Gleich F.;Gr?Newald S.;H?Berle J.;Wuh-Liang Hwu;Jalan A.;Karall D.;Lindner M.;Lund A.M.;Martinelli D.;Murphy E.;M?Hlhausen C.;Olivieri G.;Ottolenghi C.;Rodrigues E.;Rubert L.;Sarajlija A.;Schiff M.;Sokal E.;Sykutcegielska J.;Walter J.H.;Williams M.;Zeman J.;Additional Individual Contributors Of The Ucdc;The E-Imd Consortium; Posset R.; Garbade S.F.; Boy N.; Burlina A.B.; Dionisi-Vici C.; Dobbelaere D.; Garcia-Cazorla A.; de Lonlay P.; Teles E.L.; Vara R.; Mew N.A.; Batshaw M.L.; Baumgartner M.R.; McCandless S.E.; Seminara J.; Summar M.; Hoffmann G.F.; K?lker S.; Burgard P.; Berry S.A.; Burrage L.; Coughlin C.; Diaz G.A.; Gallagher R.C.; Gropman A.; Harding C.O.; Lee B.; Le Mons C.; Lawrence Merritt J.; II, Nagamani S.C.S.; Schulze A.; Stricker T.; Tuchman M.; Waisbren S.; WeisfeldAdams J.; Wong D.; Yudkoff M.; Arnoux J.; Barić I.; Bosch A.M.; Chabrol B.; Chakrapani A.; Cort?sSaladefont E.; Couce M.L.; Eyskens F.; de Laet C.; de Meirleir L.; Freisinger P.; Gleich F.; Gr?newald S.; H?berle J.; WUH-LIANG HWU; Jalan A.; Karall D.; Lindner M.; Lund A.M.; Martinelli D.; Murphy E.; M?hlhausen C.; Olivieri G.; Ottolenghi C.; Rodrigues E.; Rubert L.; Sarajlija A.; Schiff M.; Sokal E.; SykutCegielska J.; Walter J.H.; Williams M.; Zeman J.; Additional individual contributors of the UCDC; the E-IMD consortium
臺大學術典藏 2020-12-16T02:25:10Z Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum Lee C.-T.;Tung Y.-C.;Wuh-Liang Hwu;Shih J.-C.;Lin W.-H.;Wu M.-Z.;Kuo K.-T.;Yang Y.-L.;Chen H.-L.;Chen M.;Su Y.-N.;Jong Y.-J.;Liu S.-Y.;Tsai W.-Y.;Lee N.-C.; Lee C.-T.; Tung Y.-C.; WUH-LIANG HWU; Shih J.-C.; Lin W.-H.; Wu M.-Z.; Kuo K.-T.; Yang Y.-L.; Chen H.-L.; Chen M.; Su Y.-N.; Jong Y.-J.; Liu S.-Y.; Tsai W.-Y.; Lee N.-C.
臺大學術典藏 2020-12-16T02:25:09Z Genotypic and phenotypic correlations of biotinidase deficiency in the Chinese population Lee N.-C.; Huang T.-M.; Chou S.-P.; Ho H.-C.; Chang I.-F.; WUH-LIANG HWU; Chien Y.-H.; Hsu R.-H.;Chien Y.-H.;Wuh-Liang Hwu;Chang I.-F.;Ho H.-C.;Chou S.-P.;Huang T.-M.;Lee N.-C.; Hsu R.-H.
臺大學術典藏 2020-12-16T02:25:09Z Novel mutations in the mitochondrial complex I assembly gene NDUFAF5 reveal heterogeneous phenotypes Abdenur J.E.; Benke P.J.; Taft R.J.; WUH-LIANG HWU; Simon M.T.;Eftekharian S.S.;Stover A.E.;Osborne A.F.;Braffman B.H.;Chang R.C.;Wang R.Y.;Steenari M.R.;Tang S.;Wuh-Liang Hwu;Taft R.J.;Benke P.J.;Abdenur J.E.; Simon M.T.; Eftekharian S.S.; Stover A.E.; Osborne A.F.; Braffman B.H.; Chang R.C.; Wang R.Y.; Steenari M.R.; Tang S.
臺大學術典藏 2020-12-16T02:25:09Z Congenital generalized lipodystrophy in Taiwan Hsu R.-H.;Lin W.-D.;Chao M.-C.;Hsiao H.-P.;Wong S.-L.;Chiu P.-C.;Chu S.-Y.;Ke Y.-Y.;Lau B.-H.;Chien Y.-H.;Wuh-Liang Hwu;Tsai F.-J.;Wang C.-H.;Lee N.-C.; Hsu R.-H.; Lin W.-D.; Chao M.-C.; Hsiao H.-P.; Wong S.-L.; Chiu P.-C.; Chu S.-Y.; Ke Y.-Y.; Lau B.-H.; Chien Y.-H.; WUH-LIANG HWU; Tsai F.-J.; Wang C.-H.; Lee N.-C.
臺大學術典藏 2020-12-16T02:25:09Z Electrical abnormalities in dopaminergic neurons of the substantia nigra in mice with an aromatic L-amino acid decarboxylase deficiency Ho S.-Y.;Chien Y.-H.;Tsai L.-K.;Muramatsu S.-I.;Wuh-Liang Hwu;Liou H.-H.;Lee N.-C.; Ho S.-Y.; Chien Y.-H.; Tsai L.-K.; Muramatsu S.-I.; WUH-LIANG HWU; Liou H.-H.; Lee N.-C.
臺大學術典藏 2020-12-16T02:25:08Z Reply to Lutz-Bonengel et al.: Biparental mtDNA transmission is unlikely to be the result of nuclear mitochondrial DNA segments Luo S.;Alexander Valencia C.;Zhang J.;Lee N.-C.;Slone J.;Gui B.;Wang X.;Li Z.;Dell S.;Brown J.;Chen S.M.;Chien Y.-H.;Wuh-Liang Hwu;Fan P.-C.;Wong L.-J.;Atwal P.S.;Huang T.; Luo S.; Alexander Valencia C.; Zhang J.; Lee N.-C.; Slone J.; Gui B.; Wang X.; Li Z.; Dell S.; Brown J.; Chen S.M.; Chien Y.-H.; WUH-LIANG HWU; Fan P.-C.; Wong L.-J.; Atwal P.S.; Huang T.
臺大學術典藏 2020-12-16T02:25:08Z Recommendations for clinical monitoring of patients with acid sphingomyelinase deficiency (ASMD) Wasserstein M.;Dionisi-Vici C.;Giugliani R.;Wuh-Liang Hwu;Lidove O.;Lukacs Z.;Mengel E.;Mistry P.K.;Schuchman E.H.;Mcgovern M.; Wasserstein M.; Dionisi-Vici C.; Giugliani R.; WUH-LIANG HWU; Lidove O.; Lukacs Z.; Mengel E.; Mistry P.K.; Schuchman E.H.; McGovern M.

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