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Items for Author "李銘仁"
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Showing 13 items.
Collection
Date
Title
Authors
[附設醫院基因醫學部] 研究計畫
2008-04-30
研究PINK1基因突變所引起神經元凋亡之機轉 (新制多年期第1年)
李銘仁
[附設醫院基因醫學部] 研究計畫
2007-04-30
研究PINK1基因突變所引起神經元凋亡之機轉 (新制多年期第2年)
李銘仁
[附設醫院基因醫學部] 期刊論文
2007
Recent Developments in Neurofibromatosis Type 1
李銘仁
;
LEE, MING-JEN
[附設醫院基因醫學部] 期刊論文
2007
Characterization of a Familial Case with Primary Erythromelalgia from Taiwan
李銘仁
;
余幸司
;
謝松蒼
;
呂建榮
;
楊智超
;
LEE, MING-JEN
;
YU, HSIN-SU
;
HSIEH, SUNG-TSANG
;
LU, CHIEN-JUNG
;
YANG, CHIH-CHAO
[附設醫院基因醫學部] 期刊論文
2007
Acute Intermittent Porphyria with Peripheral Neuropathy: A Follow-up Study after Hematin Treatment
郭弘周
;
李銘仁
;
莊雯莉
;
黃錦章
;
KUO, HUNG-CHOU
;
LEE, MING-JEN
;
CHUANG, WEN-LI
;
HUANG, CHIN-CHANG
[附設醫院雲林分院] 期刊論文
2006
Novel Mutation of Neurofibromatosis Type 1 in a Patient with Cerebral Vasculopathy and Fatal Ischemic Stroke
湯頌君
;
李銘仁
;
鄭建興
;
葉炳強
;
TANG, SUNG-CHUN
;
LEE, MING-JEN
;
JENG, JIANN-SHING
;
YIP, PING-KEUNG
[附設醫院基因醫學部] 研究計畫
2005-07-06
利用線蟲動物模式研究台灣病人自發性SOD1 基因突變造成神經元功能退化之機轉
李銘仁
;
Lee, Ming-Jen
[流行病學研究所] 期刊論文
2005
IMPACT OF COMPLEX POLYMORPHIC SYSTEM OF ABCB1 GENE ON THE EPILEPSY TREATMENT OUTCOME.
HUNG, CHIN-CHUAN
;
TAI, JOHN, JEN
;
LIN, CHUN-JUNG
;
LEE, MING-JEN
;
LIOU, HORNG-HUEI
;
洪靚娟
;
戴政
;
林君榮
;
李銘仁
;
劉宏輝
[醫學院] 期刊論文
2005
Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Tang, Sung-Chun
;
Lee, Ming-Jen
;
Jeng, Jiann-Shing
;
Yip, Ping-Keung
;
湯頌君
;
李銘仁
;
鄭建興
;
葉炳強
[藥理學科暨研究所] 期刊論文
2005
Complex Haplotypic Effects of the Abcb1 Gene on Epilepsy Treatment Response
洪靚娟
;
李銘仁
;
林君榮
;
戴政
;
劉宏輝
;
HUNG, CHIN-CHUAN
;
LEE, MING-JEN
;
LIN, CHUN-JUNG
;
TAI, JOHN JEN
;
LIOU, HORNG-HUEI
[附設醫院神經部] 期刊論文
2005
Six Novel Npc1 Mutations in Chinese Patients with Niemann–Pick Disease Type C
楊智超
;
蘇怡寧
;
余家利
;
胡務亮
;
李銘仁
;
YANG, CHIH-CHAO
;
SU, YI-NING
;
YU, CHIA-LI
;
HWU, WUH-LIANG
;
LEE, MING-JEN
[附設醫院基因醫學部] 研究計畫
2004
Cct4 基因突變對於神經元凋亡功能之影響之研究
李銘仁
[附設醫院基因醫學部] 期刊論文
2004
Cutaneous and Sympathetic Denervation in Neonatal Rats with a Mutation in the Delta Subunit of the Cytosolic Chap Eronin-Containing T-Complex Peptide-1 Gene
許書豪
;
李銘仁
;
謝松洲
;
謝松蒼
;
HSU, SHU-HAO
;
LEE, MING-JEN
;
HSIEH, SONG-CHOU
;
FRANCESCO SCARAVILLIE
;
HSIEH, SUNG-TSANG
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