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Issue Date	Title	Author(s)	Source
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
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 ; Kuo C.-C.	Scientific Reports
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.; Liou H.-H.; MING-JEN LEE ; Fu W.-M.	PLoS ONE
2005	Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy	Tang S.-C.; MING-JEN LEE ; Jeng J.-S.; Yip P.-K.	Journal of the Neurological Sciences
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
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 ; Kuo C.-C.	PLoS Biology
2014	BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese population	Chen M.-L.; Lin C.-H.; MING-JEN LEE ; Wu R.-M.	Parkinsonism and Related Disorders
2017	Burning pain: Axonal dysfunction in erythromelalgia	Farrar M.A.; MING-JEN LEE ; Howells J.; Andrews P.I.; Lin C.S.-Y.	Pain
2019	Calebin-A induced death of malignant peripheral nerve sheath tumor cells by activation of histone acetyltransferase	MING-JEN LEE ; Tsai Y.-J.; Lin M.-Y.; You H.-L.; Kalyanam N.; Ho C.-T.; Pan M.-H.	Phytomedicine
2020	Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser	Lai H.-J.; Huang K.-C.; Liang Y.-C.; Chien K.-L.; MING-JEN LEE ; Hsieh S.-T.; Chao C.-C.; Yang C.-C.	Journal of the Formosan Medical Association
2014	A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR gene	Chen C.-H.; Huang C.-W.; MING-JEN LEE	Journal of the Formosan Medical Association
2010	Cerebral amyloid angiopathy in East and West	Chen Y.-W.; MING-JEN LEE ; Smith E.E.	International Journal of Stroke
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
2007	Characterization of a familial case with primary erythromelalgia from Taiwan	MING-JEN LEE ; Yu H.-S.; Hsieh S.-T.; Stephenson D.A.; Lu C.-J.; Yang C.-C.	Journal of Neurology
1997	Clinical and electrophysiological characteristics of inflammatory demyelinating neuropathies	MING-JEN LEE ; Chang Y.-C.; Chen R.-C.; Hsieh S.-T.	Acta Neurologica Taiwanica
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.; Chiu M.-J.; MING-JEN LEE ; Chen T.-F.; Hsu J.-L.	Journal of Alzheimer's Disease
2010	Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser	Yang N.C.-C.; MING-JEN LEE ; Chao C.-C.; Chuang Y.-T.; Lin W.-M.; Chang M.-F.; Hsieh P.-C.; Kan H.-W.; Lin Y.-H.; Yang C.-C.; Chiu M.-J.; Liou H.-H.; Hsieh S.-T.	Neurology
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.; Hsieh S.-T.; MING-JEN LEE ; Yang C.-C.; Liu C.-S.; Huang C.-C.; Lyu R.-K.; Ro L.-S.	Clinical Neurology and Neurosurgery
2005	Complex haplotypic effects of the ABCB1 gene on epilepsy treatment response	Hung C.-C.; Tai J.J.; Lin C.-J.; MING-JEN LEE ; Liou H.-H.	Pharmacogenomics
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	Hsu S.-H.; MING-JEN LEE ; Hsieh S.-C.; Scaravilli F.; Hsieh S.-T.	Neurobiology of Disease

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