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Showing items 111-120 of 345  (35 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-12-24T06:16:59Z Genetic heterozygosity and pseudodeficiency in the Pompe disease newborn screening pilot program Hwu W.-L.; Scholl T.; Labrousse P.; YIN-HSIU CHIEN; Pomponio R.J.; Keutzer J.; Lee N.-C.; Akmaev V.R.
臺大學術典藏 2020-12-24T06:16:59Z CCL18 as an alternative marker in Gaucher and Niemann-Pick disease with chitotriosidase deficiency Chang K.-L.; Hwu W.-L.; Yeh H.-Y.; Lee N.-C.; YIN-HSIU CHIEN
臺大學術典藏 2020-12-24T06:16:58Z Newborn screening for neuropathic lysosomal storage disorders Lee N.-C.; YIN-HSIU CHIEN; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:58Z Diagnoses of newborns and mothers with carnitine uptake defects through newborn screening Huang A.-C.; Hwu W.-L.; Chiu P.-C.; Lin S.-J.; Chen C.-A.; YIN-HSIU CHIEN; Tang N.L.-S.; Lee N.-C.
臺大學術典藏 2020-12-24T06:16:58Z Newborn screening healthcare information system based on service-oriented architecture Lai F.; Wang Z.; Tu C.-M.; Hsieh S.-H.; Hsieh S.-L.; YIN-HSIU CHIEN; Weng Y.-C.; Hsu K.-P.; Chen C.-H.
臺大學術典藏 2020-12-24T06:16:58Z Clinical aspects and genetic analysis of Taiwanese patients with Wiskott-Aldrich syndrome protein mutation: The first identification of X-linked thrombocytopenia in the Chinese with novel mutations Chang K.-W.; YIN-HSIU CHIEN; Wu K.-H.; Jaing T.-H.; Huang J.-L.; Lee W.-I.
臺大學術典藏 2020-12-24T06:16:57Z Newborn screening for Fabry disease by measuring GLA activity using tandem mass spectrometry YIN-HSIU CHIEN; De Jesus V.R.; Orsini J.J.; Keutzer J.; Dajnoki A.; Fekete G.; Hwu W.-L.; Lukacs Z.; M?hl A.; Zhang X.K.; Bodamer O.
臺大學術典藏 2020-12-24T06:16:57Z Reduction in imiglucerase dosage causes immediate rise of chitotriosidase activity in patients with Gaucher disease YIN-HSIU CHIEN; Lee N.-C.; Tsai F.-J.; Chao M.-C.; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:57Z Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints Ke Y.-Y.; Wang T.-J.; Lee D.-J.; Ma G.-C.; Lee N.-C.; Chen M.; YIN-HSIU CHIEN; Hwu W.-L.
臺大學術典藏 2020-12-24T06:16:57Z Enzymatic activity of methionine adenosyltransferase variants identified in patients with persistent hypermethioninemia Schulze A.; Faghfoury H.; Korman S.H.; Hwu W.-L.; Santamar?a E.; YIN-HSIU CHIEN; Fern?ndez-Irigoyen J.; Hoganson G.E.; Stabler S.P.; Allen R.H.; Wagner C.; Mudd S.H.; Corrales F.J.

Showing items 111-120 of 345  (35 Page(s) Totally)
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