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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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Showing items 96-120 of 226  (10 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-12-09T01:38:33Z Unusual spinal cord lesions in late-onset non-ketotic hyperglycinemia Wei S.-H.;Weng W.-C.;Ni-Chung Lee;Hwu W.-L.;Lee W.-T.; Wei S.-H.; Weng W.-C.; NI-CHUNG LEE; Hwu W.-L.; Lee W.-T.
臺大學術典藏 2020-12-09T01:38:33Z Congenital hypopituitarism due to POU1F1 gene mutation Ni-Chung Lee;Tsai W.-Y.;Peng S.-F.;Tung Y.-C.;Chien Y.-H.;Hwu W.-L.; NI-CHUNG LEE; Tsai W.-Y.; Peng S.-F.; Tung Y.-C.; Chien Y.-H.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:32Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; Tsao P.-N.; Chen Y.-T.; NI-CHUNG LEE
臺大學術典藏 2020-12-09T01:38:32Z Fabry disease: incidence of the common later-onset α-galactosidase A IVS4+919G→A mutation in Taiwanese newborns--superiority of DNA-based to enzyme-based newborn screening for common mutations. Chien Y.H.; NI-CHUNG LEE; Chiang S.C.; Desnick R.J.; Hwu W.L.
臺大學術典藏 2020-12-09T01:38:32Z Diagnosis of neonatal intrahepatic cholestasis caused by citrin deficiency using high-resolution melting analysis and a clinical scoring system Chen S.-T.;Su Y.-N.;Ni Y.-H.;Hwu W.-L.;Ni-Chung Lee;Chien Y.-H.;Chang C.-C.;Chen H.-L.;Chang M.-H.; Chen S.-T.; Su Y.-N.; Ni Y.-H.; Hwu W.-L.; NI-CHUNG LEE; Chien Y.-H.; Chang C.-C.; Chen H.-L.; Chang M.-H.
臺大學術典藏 2020-12-09T01:38:32Z Novel heterozygous tissue-nonspecific alkaline phosphatase (TNAP) gene mutations causing lethal perinatal hypophosphatasia Chang K.-C.; Lin P.-H.; Su Y.-N.; Peng S.S.-F.; NI-CHUNG LEE; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; Tsao P.-N.
臺大學術典藏 2020-12-09T01:38:31Z Algorithm for Pompe disease newborn screening: Results from the Taiwan screening program Chiang S.-C.; Hwu W.-L.; NI-CHUNG LEE; Hsu L.-W.; Chien Y.-H.
臺大學術典藏 2020-12-09T01:38:31Z An acidic oligopeptide displayed on AAV2 improves axial muscle tropism after systemic delivery NI-CHUNG LEE; Falk D.J.; Byrne B.J.; Conlon T.J.; Clement N.; Porvasnik S.; Jorgensen M.L.; Potter M.; Erger K.E.; Watson R.; Ghivizzani S.C.; Chiu H.-C.; Chien Y.-H.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:31Z Gene therapy for aromatic L-amino acid decarboxylase deficiency Hwu W.-L.; Muramatsu S.-I.; Tseng S.-H.; Tzen K.-Y.; NI-CHUNG LEE; Chien Y.-H.; Snyder R.O.; Byrne B.J.; Tai C.-H.; Wu R.-M.
臺大學術典藏 2020-12-09T01:38:31Z Early pathologic changes and responses to treatment in patients with later-onset Pompe disease Chien Y.-H.; NI-CHUNG LEE; Huang P.-H.; Lee W.-T.; Thurberg B.L.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:30Z Fatty acid oxidation disorders in a chinese population in Taiwan Hwu W.-L.; Chien Y.-H.; NI-CHUNG LEE; Chao M.-C.; Chen L.-C.; Chen L.-H.; Chien C.-C.; Ho H.-C.; Suen J.-H.
臺大學術典藏 2020-12-09T01:38:30Z Late onset of symptoms in an atypical patient with the cblJ inborn error of vitamin B12 metabolism: Diagnosis and novel mutation revealed by exome sequencing Kim J.C.; NI-CHUNG LEE; Hwu P.W.L.; Chien Y.-H.; Fahiminiya S.; Majewski J.; Watkins D.; Rosenblatt D.S.
臺大學術典藏 2020-12-09T01:38:30Z A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a child Liu H.-M.; Tsai L.-P.; Chien Y.-H.; Wu J.-F.; Weng W.-C.; Peng S.-F.; Wu E.-T.; Huang P.-H.; Lee W.-T.; Tsai I.-J.; Hwu W.-L.; NI-CHUNG LEE
臺大學術典藏 2020-12-09T01:38:30Z Long-term efficacy of miglustat in paediatric patients with Niemann-Pick disease type C Chien Y.H.; Peng S.F.; Yang C.C.; NI-CHUNG LEE; Tsai L.K.; Huang A.C.; Su S.C.; Tseng C.C.; Hwu W.L.
臺大學術典藏 2020-12-09T01:38:29Z Promising outcomes in glutaric aciduria type i patients detected by newborn screening Lee C.-S.; Chien Y.-H.; Peng S.-F.; Cheng P.-W.; Chang L.-M.; Huang A.-C.; Hwu W.-L.; NI-CHUNG LEE
臺大學術典藏 2020-12-09T01:38:29Z Newborn screening for citrin deficiency and carnitine uptake defect using second-tier molecular tests Wang L.-Y.; Chen N.-I.; Chen P.-W.; Chiang S.-C.; Hwu W.-L.; NI-CHUNG LEE; Chien Y.-H.
臺大學術典藏 2020-12-09T01:38:29Z Clinical application of massively parallel sequencing in the molecular diagnosis of glycogen storage diseases of genetically heterogeneous origin Wang J.; Cui H.; NI-CHUNG LEE; Hwu W.-L.; Chien Y.-H.; Craigen W.J.; Wong L.-J.; Zhang V.W.
臺大學術典藏 2020-12-09T01:38:29Z AADC deficiency. Occurring in humans, modeled in rodents. Hwu W.-L.; NI-CHUNG LEE; Chien Y.-H.; Muramatsu S.-I.; Ichinose H.
臺大學術典藏 2020-12-09T01:38:28Z Carnitine Uptake Defect (Primary Carnitine Deficiency): Risk in Genotype-Phenotype Correlation Chen Y.-C.; Chien Y.-H.; Chen P.-W.; Leung-Sang Tang N.; Chiu P.-C.; Hwu W.-L.; NI-CHUNG LEE
臺大學術典藏 2020-12-09T01:38:28Z Regulation of the dopaminergic system in a murine model of aromatic l-amino acid decarboxylase deficiency NI-CHUNG LEE; Shieh Y.-D.; Chien Y.-H.; Tzen K.-Y.; Yu I.-S.; Chen P.-W.; Hu M.-H.; Hu M.-K.; Muramatsu S.-I.; Ichinose H.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:28Z Mitochondrial depletion causes neonatal-onset leigh syndrome, myopathy, and renal tubulopathy Lee I.-C.; NI-CHUNG LEE; Lu J.-J.; Su P.-H.
臺大學術典藏 2020-12-09T01:38:28Z Serial cytokine expressions in infants with incontinentia pigmenti Liao S.-L.; Lai S.-H.; Huang J.-L.; NI-CHUNG LEE; Lee W.-I.
臺大學術典藏 2020-12-09T01:38:27Z Pompe disease: Early diagnosis and early treatment make a difference Chien Y.-H.; Hwu W.-L.; NI-CHUNG LEE
臺大學術典藏 2020-12-09T01:38:27Z Lung toxicity of hydroxypropyl-β-cyclodextrin infusion Chien Y.-H.; Shieh Y.-D.; Yang C.-Y.; NI-CHUNG LEE; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:27Z AADC Deficiency: Occurring in Humans; Modeled in Rodents; Treated in Patients Hwu W.-L.; NI-CHUNG LEE; Shieh Y.-D.; Tzen K.-Y.; Chen P.-W.; Muramatsu S.-I.; Ichinose H.; Chien Y.-H.

Showing items 96-120 of 226  (10 Page(s) Totally)
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