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

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Institution	Date	Title	Author
臺大學術典藏	2022-09-20T06:49:29Z	Efficacy, safety and tolerability of ongoing statin plus ezetimibe versus doubling the ongoing statin dose in hypercholesterolemic Taiwanese patients: An open-label, randomized clinical trial	Yu C.-C.; Lai W.-T.; Shih K.-C.; Lin T.-H.; Lu C.-H.; Lai H.-J.; Hanson M.E.; HWANG, JUEY-JEN
臺大學術典藏	2022-04-28T12:31:22Z	Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser	Lai H.-J.; Huang K.-C.; Liang Y.-C.; KUO-LIONG CHIEN; Lee M.-J.; Hsieh S.-T.; Chao C.-C.; Yang C.-C.
臺大學術典藏	2022-02-15T06:22:51Z	Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy	Lin C.-H.; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; CHIH-CHIANG CHAN; Ke Y.-C.; Chao C.-C.; Hsieh S.-T.; Farrer M.; Wu R.-M.
臺大學術典藏	2022-02-15T06:22:47Z	An electrophysiological perspective on Parkinson’s disease: symptomatic pathogenesis and therapeutic approaches	Lee L.-H.N.; Huang C.-S.; Chuang H.-H.; Lai H.-J.; Yang C.-K.; Yang Y.-C.; CHUNG-CHIN KUO
臺大學術典藏	2021-11-26T05:56:33Z	Increase of hyperpolarization-activated cyclic nucleotide-gated current in the aberrant excitability of spinal muscular atrophy	Lai H.-J.; Chen C.-L.; LI-KAI TSAI
臺大學術典藏	2021-11-16T02:44:01Z	Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy	CHIN-HSIEN LIN; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; Chan C.-C.; Ke Y.-C.; Chao C.-C.; Hsieh S.-T.; Farrer M.; Wu R.-M.
臺大學術典藏	2021-11-03T01:43:05Z	Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy	Lin C.-H.; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; Chan C.-C.; Ke Y.-C.; Chao C.-C.; Hsieh S.-T.; Farrer M.; RUEY-MEEI WU
臺大學術典藏	2021-09-23T03:48:58Z	Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy	Lin C.-H.; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; Chan C.-C.; Ke Y.-C.; CHI-CHAO CHAO; Hsieh S.-T.; Farrer M.; Wu R.-M.
臺大學術典藏	2021-09-09T07:52:48Z	Efficacy, safety and tolerability of ongoing statin plus ezetimibe versus doubling the ongoing statin dose in hypercholesterolemic Taiwanese patients: An open-label, randomized clinical trial	CHIH-CHIEH YU; Lai W.-T.; Shih K.-C.; Lin T.-H.; Lu C.-H.; Lai H.-J.; Hanson M.E.; Hwang J.-J.
臺大學術典藏	2021-08-20T08:19:38Z	Frail phenotype is associated with distinct quantitative electroencephalographic findings among end-stage renal disease patients: An observational study	CHIA-TER CHAO; Lai H.-J.; Tsai H.-B.; Yang S.-Y.; Huang J.-W.

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