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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 151-175 of 512  (21 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-12-24T06:16:53Z Rapid progressive course of later-onset Pompe disease in Chinese patients Hwu W.-L.; Jong Y.-J.; Chen S.-S.; Kuo Y.-T.; Lin S.-P.; Chiang S.-C.; Lee N.-C.; YIN-HSIU CHIEN; Yang C.-C.
臺大學術典藏 2020-12-24T06:16:52Z 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. YIN-HSIU CHIEN; Lee N.C.; Chiang S.C.; Desnick R.J.; Hwu W.L.
臺大學術典藏 2020-12-24T06:16:52Z Diagnosis of neonatal intrahepatic cholestasis caused by citrin deficiency using high-resolution melting analysis and a clinical scoring system Chang M.-H.; Chen H.-L.; Chang C.-C.; YIN-HSIU CHIEN; Lee N.-C.; Hwu W.-L.; Ni Y.-H.; Su Y.-N.; Chen S.-T.
臺大學術典藏 2020-12-24T06:16:51Z Gene therapy for aromatic L-amino acid decarboxylase deficiency Wu R.-M.; Tai C.-H.; Byrne B.J.; YIN-HSIU CHIEN; Snyder R.O.; Lee N.-C.; Tzen K.-Y.; Tseng S.-H.; Muramatsu S.-I.; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:51Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Lee N.-C.; Chen Y.-T.; Tsao P.-N.; Hsieh W.-S.; Chen C.-Y.; Chou H.-C.; Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; YIN-HSIU CHIEN
臺大學術典藏 2020-12-24T06:16:51Z Early pathologic changes and responses to treatment in patients with later-onset Pompe disease Hwu W.-L.; Thurberg B.L.; Huang P.-H.; Lee W.-T.; Lee N.-C.; YIN-HSIU CHIEN
臺大學術典藏 2020-12-24T06:16:50Z An acidic oligopeptide displayed on AAV2 improves axial muscle tropism after systemic delivery Ghivizzani S.C.; Watson R.; Erger K.E.; Jorgensen M.L.; Potter M.; Clement N.; Porvasnik S.; Conlon T.J.; Lee N.-C.; Falk D.J.; Byrne B.J.; Chiu H.-C.; YIN-HSIU CHIEN; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:49Z Algorithm for Pompe disease newborn screening: Results from the Taiwan screening program Chiang S.-C.; Hwu W.-L.; Lee N.-C.; Hsu L.-W.; YIN-HSIU CHIEN
臺大學術典藏 2020-12-24T06:16:48Z 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 Rosenblatt D.S.; Watkins D.; Majewski J.; Fahiminiya S.; YIN-HSIU CHIEN; Hwu P.W.L.; Lee N.-C.; Kim J.C.
臺大學術典藏 2020-12-24T06:16:46Z Fatty acid oxidation disorders in a chinese population in Taiwan Ho H.-C.; Chien C.-C.; Chen L.-H.; Chao M.-C.; Chen L.-C.; Lee N.-C.; YIN-HSIU CHIEN; Suen J.-H.; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:45Z 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.; Lee N.-C.; YIN-HSIU CHIEN
臺大學術典藏 2020-12-24T06:16:45Z Clinical application of massively parallel sequencing in the molecular diagnosis of glycogen storage diseases of genetically heterogeneous origin Wang J.; Cui H.; Lee N.-C.; Hwu W.-L.; YIN-HSIU CHIEN; Craigen W.J.; Wong L.-J.; Zhang V.W.
臺大學術典藏 2020-12-24T06:16:43Z Lung toxicity of hydroxypropyl-β-cyclodextrin infusion Lee N.-C.; Hwu W.-L.; Yang C.-Y.; Shieh Y.-D.; YIN-HSIU CHIEN
臺大學術典藏 2020-12-24T06:16:43Z Carnitine Uptake Defect (Primary Carnitine Deficiency): Risk in Genotype-Phenotype Correlation Chen Y.-C.; YIN-HSIU CHIEN; Chen P.-W.; Leung-Sang Tang N.; Chiu P.-C.; Hwu W.-L.; Lee N.-C.
臺大學術典藏 2020-12-24T06:16:42Z Pompe disease: Early diagnosis and early treatment make a difference Lee N.-C.; YIN-HSIU CHIEN; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:41Z Efficacy and safety of intermittent hemodialysis in infants and young children with inborn errors of metabolism Tsai I.-J.; Hwu W.-L.; Huang S.-C.; Lee N.-C.; Wu E.-T.; YIN-HSIU CHIEN; Tsau Y.-K.
臺大學術典藏 2020-12-24T06:16:41Z Outcome of early-treated type III Gaucher disease patients Hwu W.-L.; Shun C.-T.; Chao M.-C.; Leung J.H.; Lee N.-C.; YIN-HSIU CHIEN; Wong S.-L.; Sheen J.-M.; Tsai F.-J.; Peng S.-F.
臺大學術典藏 2020-12-24T06:16:41Z AADC Deficiency: Occurring in Humans; Modeled in Rodents; Treated in Patients Hwu W.-L.; Lee N.-C.; Shieh Y.-D.; Tzen K.-Y.; Chen P.-W.; Muramatsu S.-I.; Ichinose H.; YIN-HSIU CHIEN
臺大學術典藏 2020-12-24T06:16:40Z Application of mass spectrometry in newborn screening: About both small molecular diseases and lysosomal storage diseases Hsu L.-W.; Wang S.-F.; Chiang S.-C.; Lee N.-C.; YIN-HSIU CHIEN; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:40Z Prominent vacuolation of the eyelid levator muscle in an early-treated child with infantile-onset Pompe disease Hwu W.-L.; Tsai F.-J.; Thurberg B.L.; Tsai Y.-J.; YIN-HSIU CHIEN; Lee N.-C.
臺大學術典藏 2020-12-24T06:16:39Z Treatment of congenital neurotransmitter deficiencies by intracerebral ventricular injection of an adeno-associated virus serotype 9 vector Lee N.-C.; YIN-HSIU CHIEN; Hu M.-H.; Liu W.-S.; Chen P.-W.; Wang W.-H.; Tzen K.-Y.; Byrne B.J.; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:38Z Baseline urinary glucose tetrasaccharide concentrations in patients with infantile- and late-onset pompe disease identified by newborn screening Young S.P.; Kishnani P.S.; Millington D.S.; Vaisnins A.E.; Zhang H.; YIN-HSIU CHIEN; Goldstein J.L.; Hwu W.-L.; Smith P.B.; Lee N.-C.; Chiang S.-C.; Tolun A.A.
臺大學術典藏 2020-12-24T06:16:38Z Diagnosis of aromatic l-amino acid decarboxylase deficiency by measuring 3-O-methyldopa concentrations in dried blood spots Chen P.-W.; Lee N.-C.; YIN-HSIU CHIEN; Wu J.-Y.; Wang P.-C.; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:37Z Long-term prognosis of patients with infantile-onset pompe disease diagnosed by newborn screening and treated since birth Tsai F.-J.; Chen C.-A.; Lee N.-C.; YIN-HSIU CHIEN; Tsai W.-H.; Shieh J.-Y.; Huang H.-J.; Hsu W.-C.; Tsai T.-H.; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:36Z Mortality, disability, and intensive care in patients with mitochondrial 3243A>G mutation Lee P.-L.; Lu C.-J.; Wang T.-J.; Chu S.-Y.; Lin S.-J.; Hsiue H.-C.; Lee N.-C.; Tsai H.-B.; Yang C.-C.; Wu C.-S.; Lee W.-T.; Weng W.-C.; Fan P.-C.; YIN-HSIU CHIEN; Hwu W.-L.; Hung K.-L.; Huang C.-C.; Chen C.-H.

Showing items 151-175 of 512  (21 Page(s) Totally)
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