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Showing results 1 to 20 of 68
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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
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