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Showing items 286-295 of 1753  (176 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-12-21T08:16:39Z AngioJet thrombectomy to salvage thrombosed native dialysis fistulas WEN-JONE CHEN; Wen S.-C.;Pu S.-Y.;Tsai K.-C.;Yang C.-C.;Wu C.-C.;Wen-Jone Chen; Wen S.-C.; Pu S.-Y.; Tsai K.-C.; Yang C.-C.; Wu C.-C.
臺大學術典藏 2020-12-18T05:21:14Z Levamisole-induced multifocal inflammatory leukoencephalopathy: Clinical characteristics, outcome, and impact of treatment in 31 patients Wu K.-D.; Hwang J.-J.; YEN-HUNG LIN; Yang C.-C.; Liu H.-M.; Wu V.-C.; Huang J.-W.; Lien H.-C.; Hsieh S.-T.
臺大學術典藏 2020-12-18T02:21:54Z Multiple Sclerosis With Childhood Onset: Report of 21 Cases in Taiwan Weng W.-C.; Yang C.-C.; Yu T.-W.; Shen Y.-Z.; WANG-TSO LEE
臺大學術典藏 2020-12-18T02:21:43Z Mortality, disability, and intensive care in patients with mitochondrial 3243A>G mutation WANG-TSO LEE; Wu C.-S.; Hsiue H.-C.; Lee N.-C.; Tsai H.-B.; Yang C.-C.; Weng W.-C.; Fan P.-C.; Chien Y.-H.; Hwu W.-L.; Hung K.-L.; Huang C.-C.; Chen C.-H.; Lin S.-J.; Chu S.-Y.; Wang T.-J.; Lu C.-J.; Lee P.-L.
臺大學術典藏 2020-12-16T02:26:17Z Two novel mutations in the α-galactosidase A gene in Chinese patients with Fabry disease Yang C.-C.;Lai L.-W.;Whitehair O.;Wuh-Liang Hwu;Chiang S.-C.;Lien Y.-H.H.; Yang C.-C.; Lai L.-W.; Whitehair O.; WUH-LIANG HWU; Chiang S.-C.; Lien Y.-H.H.
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 2020-12-16T02:26:08Z 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 2020-12-16T02:26:06Z 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 2020-12-16T02:25:59Z Valproic acid treatment in six patients with spinal muscular atrophy [5] Tsai L.-K.;Yang C.-C.;Wuh-Liang Hwu;Li H.; Tsai L.-K.; Yang C.-C.; WUH-LIANG HWU; Li H.

Showing items 286-295 of 1753  (176 Page(s) Totally)
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