臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Showing items 186-195 of 345 (35 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2020-12-24T06:16:23Z	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.; YIN-HSIU CHIEN; Hwu W.-L.; Fan P.-C.; Wong L.-J.; Atwal P.S.; Huang T.
臺大學術典藏	2020-12-24T06:16:22Z	Monitoring of liver stiffness by transient elastography during the treatment of Gaucher disease	Wu J.-F.; YIN-HSIU CHIEN; Lee C.-S.; Hsu C.-T.; Chin C.-Y.
臺大學術典藏	2020-12-24T06:16:21Z	Gene therapy improves brain white matter in aromatic l-amino acid decarboxylase deficiency	Hwu W.-L.; Tseng W.-Y.I.; Peng S.-F.; Hsu Y.-C.; Tseng C.-H.; YIN-HSIU CHIEN; Lee N.-C.
臺大學術典藏	2020-12-24T06:16:20Z	Fabry disease cardiac variant IVS4+919 G>A is associated with multiple cardiac gene variants in patients with severe cardiomyopathy and fatal arrhythmia	YIN-HSIU CHIEN; Chen N.-Q.; Tsai W.-H.; Juang J.-M.J.; Shun C.-T.; Chen Y.-S.; Hwu W.-L.; Lee N.-C.
臺大學術典藏	2020-12-24T06:16:20Z	High incidence of co-existing GLA variants and stroke susceptibility	YIN-HSIU CHIEN; Hwu W.-L.
臺大學術典藏	2020-12-24T06:16:20Z	A review of aromatic l-amino acid decarboxylase (AADC) deficiency in Taiwan	Lee N.-C.; YIN-HSIU CHIEN; Hwu W.-L.
臺大學術典藏	2020-12-24T06:16:20Z	Rare Concurrence of Two Congenital Disorders: Miller-Dieker Syndrome and T-Cell Lymphopenia	Feng W.-K.; Lee Y.-C.; Chee S.-Y.; Guo J.-W.; Huang C.-J.; YIN-HSIU CHIEN
臺大學術典藏	2020-12-24T06:16:19Z	Critical Trio Exome Benefits In-Time Decision-Making for Pediatric Patients with Severe Illnesses?	Lee N.-C.; Lai F.; Hsiung H.-C.; Tsai W.-H.; Chiu P.-C.; Chou Y.-Y.; Lee C.-H.; Chen C.-N.; Chang T.-M.; Hsieh W.-S.; Lin S.-P.; Tsai I.-J.; Fan P.-C.; Tsao P.-N.; Chou H.-C.; Chen N.-Q.; Wu E.-T.; Hwu W.-L.; YIN-HSIU CHIEN; Hsu C.; Chen T.-F.
臺大學術典藏	2020-12-24T06:16:18Z	Clinical features of Pompe disease with motor neuronopathy	Tsai L.-K.; Hwu W.-L.; Lee N.-C.; Huang P.-H.; YIN-HSIU CHIEN
臺大學術典藏	2020-12-24T06:16:18Z	GAA variants and phenotypes among 1,079 patients with Pompe disease: Data from the Pompe Registry	Leslie N.; Kimonis V.E.; Clemens P.R.; Abbott M.-A.; Llerena J.; Jr.; YIN-HSIU CHIEN; van der Ploeg A.T.; Reuser A.J.J.; Maruti S.S.; Sanson B.-J.; Araujo R.; Periquet M.; Toscano A.; Kishnani P.S.; on behalf of the Pompe Registry Sites

Showing items 186-195 of 345 (35 Page(s) Totally)
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