| Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
|---|---|---|---|---|---|---|
| 2007 | Acute intermittent porphyria with peripheral neuropathy: A follow-up study after hematin treatment | Kuo H.-C.; MING-JEN LEE ; Chuang W.-L.; Huang C.-C. | Journal of the Neurological Sciences | 18 | 17 | |
| 2019 | Anomalous enhancement of resurgent Na+ currents at high temperatures by SCN9A mutations underlies the episodic heat-enhanced pain in inherited erythromelalgia | Huang C.-W.; Lai H.-J.; Huang P.-Y.; MING-JEN LEE ; Chung-Chin Kuo | Scientific Reports | 3 | 12 | |
| 2017 | Antagonism of proteasome inhibitor-induced heme oxygenase-1 expression by PINK1 mutation | Sheng X.-J.; Tu H.-J.; Chien W.-L.; Kang K.-H.; Lu D.-H.; HORNG-HUEI LIOU ; MING-JEN LEE ; WEN-MEI FU | PLoS ONE | 11 | 13 | |
| 2005 | Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy | SUNG-CHUN TANG ; MING-JEN LEE ; JIANN-SHING JENG ; Yip P.-K. | Journal of the Neurological Sciences | 21 | 15 | |
| 1991 | Biochemical events coupled to the activation of serotonin receptors in brain regions of the rat | Wei J.-W.; MING-JEN LEE ; Yeh S.-R. | Chinese Journal of Physiology | 1 | 0 | |
| 2016 | The Biophysical Basis Underlying Gating Changes in the p.V1316A Mutant Nav1.7 Channel and the Molecular Pathogenesis of Inherited Erythromelalgia | Huang C.-W.; Lai H.-J.; Huang P.-Y.; MING-JEN LEE ; Chung-Chin Kuo | PLoS Biology | 8 | 4 | |
| 2014 | BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese population | Chen M.-L.; CHIN-HSIEN LIN ; MING-JEN LEE ; RUEY-MEEI WU | Parkinsonism and Related Disorders | 24 | 18 | |
| 2017 | Burning pain: Axonal dysfunction in erythromelalgia | Farrar M.A.; MING-JEN LEE ; Howells J.; Andrews P.I.; Lin C.S.-Y. | Pain | 11 | 10 | |
| 2019 | Calebin-A induced death of malignant peripheral nerve sheath tumor cells by activation of histone acetyltransferase | MING-JEN LEE ; MING-JEN LEE; Tsai, Yi Jane; Lin, May Yao; You, Huey Ling; MIN-HSIUNG PAN; Kalyanam, Nagabhushanam; Ho, Chi Tang; MING-JEN LEE; Tsai, Yi Jane; Lin, May Yao; You, Huey Ling; MIN-HSIUNG PAN; MIN-HSIUNG PAN | Phytomedicine | 24 | 22 | |
| 2020 | 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 ; MING-JEN LEE ; SUNG-TSANG HSIEH ; CHI-CHAO CHAO ; Yang C.-C. | Journal of the Formosan Medical Association | 11 | 9 | |
| 2014 | A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR gene | CHIH-HAO CHEN ; Huang C.-W.; MING-JEN LEE | Journal of the Formosan Medical Association | 5 | 4 | |
| 2010 | Cerebral amyloid angiopathy in East and West | Chen Y.-W.; MING-JEN LEE ; Smith E.E. | International Journal of Stroke | 25 | 25 | |
| 2020 | Changes of resurgent Na+ currents in the Nav1.4 channel resulting from an SCN4A mutation contributing to sodium channel myotonia | Huang C.-W.; Lai H.-J.; Lin P.-C.; MING-JEN LEE | International Journal of Molecular Sciences | 5 | 5 | |
| 2007 | Characterization of a familial case with primary erythromelalgia from Taiwan | MING-JEN LEE ; Yu H.-S.; SUNG-TSANG HSIEH ; Stephenson D.A.; Lu C.-J.; Yang C.-C. | Journal of Neurology | 46 | 41 | |
| 1997 | Clinical and electrophysiological characteristics of inflammatory demyelinating neuropathies | MING-JEN LEE ; Chang Y.-C.; Chen R.-C.; Hsieh S.-T. | Acta Neurologica Taiwanica | 1 | ||
| 2011 | Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's disease | Wu Y.-Y.; Cheng I.H.-J.; Lee C.-C.; MING-JANG CHIU ; MING-JEN LEE ; TA-FU CHEN ; Hsu J.-L. | Journal of Alzheimer's Disease | 10 | 9 | |
| 2008 | Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese | Chen S.-R.; Lin K.-P.; Kuo H.-C.; Chen C.-M.; SUNG-TSANG HSIEH ; MING-JEN LEE ; Yang C.-C.; Liu C.-S.; Huang C.-C.; Lyu R.-K.; Ro L.-S. | Clinical Neurology and Neurosurgery | 7 | 5 | |
| 2005 | Complex haplotypic effects of the ABCB1 gene on epilepsy treatment response | Hung C.-C.; Tai J.J.; Lin C.-J.; MING-JEN LEE ; HORNG-HUEI LIOU | Pharmacogenomics | 115 | 101 | |
| 2004 | Cutaneous and sympathetic denervation in neonatal rats with a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 gene | SHU-HAO HSU ; MING-JEN LEE ; SONG-CHOU HSIEH ; Scaravilli F.; SUNG-TSANG HSIEH | Neurobiology of Disease | 4 | 4 | |
| 2019 | Detrimental effects of intracerebral haemorrhage on patients with CADASIL harbouring NOTCH3 R544C mutation | Chen C.-H.; SUNG-CHUN TANG ; Cheng Y.-W.; Tsai H.-H.; Chi N.-F.; Sung P.-S.; Yeh H.-L.; Lien L.-M.; Lin H.-J.; MING-JEN LEE ; Hu C.-J.; Chiou H.-Y.; JIANN-SHING JENG | 11 | 11 |
