公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
2016 | Microglia-derived cytokines/chemokines are involved in the enhancement of LPS-induced loss of nigrostriatal dopaminergic neurons in DJ-1 knockout mice | Chien C.-H.; MING-JEN LEE ; Liou H.-C.; HORNG-HUEI LIOU ; WEN-MEI FU | PLoS ONE | 42 | 38 | |
2010 | The microRNA spectrum in 12 body fluids | Weber J.A.; Baxter D.H.; Zhang S.; Huang D.Y.; KUO-HOW HUANG ; MING-JEN LEE ; Galas D.J.; Wang K. | Clinical Chemistry | 2188 | 1976 | |
2013 | Microstructural integrity of cerebral fiber tracts in hereditary spastic paraparesis with SPG11 mutation | MING-KAI PAN ; Huang S.-C.; Lo Y.-C.; Yang C.-C.; Cheng T.-W.; Yang C.-C.; Hua M.-S.; MING-JEN LEE ; WEN-YIH TSENG | American Journal of Neuroradiology | 11 | 11 | |
2013 | Molecular pathogenesis of neurofibromatosis type 1 | MING-JEN LEE ; Etheridge A.; Galas D.J.; Wang K. | Neurofibromatosis Type 1: Symptoms, Treatment and Prognosis | 0 | ||
2015 | Motor and Sensory Axon Excitability Properties from the Median and Ulnar Nerves and the Effects of Age on These Properties | Lai H.-J.; Chiang Y.-W.; MING-JEN LEE | Journal of Clinical Neurophysiology | 6 | 6 | |
2015 | Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan | MING-JEN LEE ; YA-FANG CHEN ; PI-CHUAN FAN ; KUO-CHUAN WANG ; Wang K.; Wang J.; MENG-FAI KUO | Journal of the Neurological Sciences | 27 | 25 | |
2002 | Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4] | MING-JEN LEE ; Huang Y.-C.; Sweeney M.G.; Wood N.W.; Reilly M.M.; Yip P.-K. | Journal of Neurology | 8 | 5 | |
2008 | Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum | MING-JEN LEE ; Cheng T.-W.; Hua M.-S.; MING-KAI PAN ; Wang J.; Stephenson D.A.; Yang C.-C. | Journal of Neurology, Neurosurgery and Psychiatry | 18 | 17 | |
2021 | Myopathy associated with COVID-19 | Hsueh, Sung-Ju; MING-JEN LEE ; HSIN-SHUI CHEN ; Chang, Kai Chieh | Journal of the Formosan Medical Association | 7 | 4 | |
2008 | Nerve function and dysfunction in acute intermittent porphyria | Lin C.S.-Y.; Krishnan A.V.; MING-JEN LEE ; Zagami A.S.; You H.-L.; Yang C.-C.; Bostock H.; Kiernan M.C. | Brain | 70 | 58 | |
2011 | Neurological complications of acute intermittent porphyria | Kuo H.-C.; Huang C.-C.; Chu C.-C.; MING-JEN LEE ; Chuang W.-L.; Wu C.-L.; Wu T.; Ning H.-C.; Liu C.-Y. | European Neurology | 22 | 21 | |
2009 | Notch signaling and CADASIL | SUNG-CHUN TANG ; JIANN-SHING JENG ; MING-JEN LEE ; Yip P.-K. | Acta Neurologica Taiwanica | 13 | 0 | |
2006 | Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke | SUNG-CHUN TANG ; MING-JEN LEE ; JIANN-SHING JENG ; Yip P.-K. | Journal of the Neurological Sciences | 10 | 8 | |
2013 | A Novel SCN9A Mutation Responsible for Primary Erythromelalgia and Is Resistant to the Treatment of Sodium Channel Blockers | Wu M.-T.; Huang P.-Y.; Yen C.-T.; Chen C.-C.; MING-JEN LEE | PLoS ONE | 58 | 49 | |
2020 | A novel treatment modality for malignant peripheral nerve sheath tumor using a dual-effect liposome to combine photodynamic therapy and chemotherapy | Peng, P.-C.; Tsai, T.; Chien, H.-F.; CHIN-TIN CHEN ; MING-JEN LEE | Pharmaceutics | 11 | 11 | |
2014 | A novel XK gene mutation in a Taiwanese family with McLeod syndrome | Chen P.-Y.; Lai S.-C.; Yang C.-C.; MING-JEN LEE ; Chiu Y.-H.; Yan S.-H.; Lu C.-S.; Yeh T.-H. | Journal of the Neurological Sciences | 8 | 5 | |
2013 | Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemia | MING-JEN LEE ; KUO-LIONG CHIEN ; MING-FONG CHEN ; Stephenson D.A.; TA-CHEN SU | Clinica Chimica Acta | 17 | 14 | |
2012 | PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort | Lee Y.-C.; MING-JEN LEE ; Yu H.-Y.; Chen C.; Hsu C.-H.; Lin K.-P.; Liao K.-K.; Chang M.-H.; Liao Y.-C.; Soong B.-W. | PLoS ONE | 46 | 38 | |
2011 | Purple pigments: The pathophysiology of acute porphyric neuropathy | Lin C.S.-Y.; MING-JEN LEE ; Park S.B.; Kiernan M.C. | Clinical Neurophysiology | 45 | 31 | |
2008 | Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonography | Ma G.-C.; Chang S.-D.; Chang Y.; Chang S.-P.; Yang C.-W.; MING-JEN LEE ; Lee T.-H.; Chen M. | Fertility and Sterility | 4 | 3 |