研究成果


第 1 到 79 筆結果，共 79 筆。

公開日期標題作者來源出版物scopusWOS全文
12023Impact of Vutrisiran on Quality of Life and Physical Function in Patients with Hereditary Transthyretin-Mediated Amyloidosis with PolyneuropathyObici, Laura; Ajroud-Driss, Senda; Lin, Kon-Ping; Berk, John L; Gillmore, Julian D; Kale, Parag; Koike, Haruki; Danese, David; Aldinc, Emre; Chen, Chongshu; Vest, John; Adams, David; MING-JEN LEE ; HSUEH-WEN HSUEH ; LI-KAI TSAI ; JEN-JEN SU ; Chou, Hsi-Chieh; CHI-CHAO CHAO ; SUNG-TSANG HSIEH Neurology and therapy31
22023Cardiomyopathy Efficacy of Tafamidis in Patients with Ala97Ser Hereditary Transthyretin Cardiac Amyloidosis: A Six-Month Follow-Up StudyCHENG-HSUAN TSAI ; Yu, An-Li; Wu, Yuan-Kun Aden; MAO-YUAN SU ; MEI-FANG CHENG ; Chou, Chia-Hung; CHIA-TUNG SHUN ; HSUEH-WEN HSUEH ; JYH-MING JIMMY JUANG ; MING-JEN LEE ; PING-HUEI TSENG ; SUNG-TSANG HSIEH ; CHI-CHAO CHAO ; YEN-HUNG LIN Acta Cardiologica Sinica11
32023Tafamidis Treatment Decreases 99mTc-Pyrophosphate Uptake in Patients With Hereditary Ala97Ser Transthyretin Amyloid CardiomyopathyYu, An-Li; Chen, Yi-Chieh; CHENG-HSUAN TSAI ; CHI-CHAO CHAO ; MAO-YUAN SU ; JYH-MING JIMMY JUANG ; MING-JEN LEE ; SUNG-TSANG HSIEH ; MEI-FANG CHENG ; YEN-HUNG LIN JACC. Cardiovascular imaging44
42022EXPLORE B: A prospective, long-term natural history study of patients with acute hepatic porphyria with chronic symptomsCassiman, David; Kauppinen, Raili; Monroy, Susana; MING-JEN LEE ; Bonkovsky, Herbert L; Thapar, Manish; Guillén-Navarro, Encarna; Minder, Anna-Elisabeth; Hale, Cecilia; Sweetser, Marianne T; Ivanova, AnetaJournal of inherited metabolic disease41
52022Comparison of clinical and neuroimaging features between NOTCH3 mutations and nongenetic spontaneous intracerebral haemorrhageCHIH-HAO CHEN ; Chu, Yung-Tsai; YA-FANG CHEN ; Ko, Tzu-Yu; Cheng, Yu-Wen; MING-JEN LEE ; PEI-LUNG CHEN ; SUNG-CHUN TANG ; JIANN-SHING JENG European journal of neurology44
62022Kinetic Alterations in Resurgent Sodium Currents of Mutant Nav1.4 Channel in Two Patients Affected by Paramyotonia CongenitaMING-JEN LEE ; Lin, Pi-Chen; Lin, Ming-Hong; Chiou, Hsin-Ying Clair; Wang, Kai; Huang, Chiung-WeiBiology00
72022Recent Advances in RNA Therapy and Its Carriers to Treat the Single-Gene Neurological DisordersMING-JEN LEE ; Lee, Inyoul; Wang, KaiBiomedicines95
82021Cannabidiol Selectively Binds to the Voltage-Gated Sodium Channel Nav1.4 in Its Slow-Inactivated State and Inhibits Sodium CurrentHuang, Chiung-Wei; Lin, Pi-Chen; Chen, Jian-Lin; MING-JEN LEE Biomedicines85
92021DNA hypermethylation involves in the down-regulation of chloride intracellular channel 4 (CLIC4) induced by photodynamic therapyChiang, Pei Chi; Li, Pei Tzu; MING-JEN LEE ; CHIN-TIN CHEN Biomedicines11
102021Myopathy associated with COVID-19Hsueh, Sung-Ju; MING-JEN LEE ; HSIN-SHUI CHEN ; Chang, Kai ChiehJournal of the Formosan Medical Association74
112021Changes in Resurgent Sodium Current Contribute to the Hyperexcitability of Muscles in Patients with Paramyotonia CongenitaHuang, Chiung-Wei; Lai, Hsing-Jung; Lin, Pi-Chen; MING-JEN LEE Biomedicines54
122021Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension studyAdams D.; Polydefkis M.; González-Duarte A.; Wixner J.; Kristen A.V.; Schmidt H.H.; Berk J.L.; Losada López I.A.; Dispenzieri A.; Quan D.; Conceição I.M.; Stephant M.; Echaniz-Laguna A.; Becquemont L.; Beaudonnet G.; Algalarrondo V.; Eliahou L.; Signate A.; Berthelot E.; Inamo J.; Vervoitte L.; Slama M.S.; Focseneanu C.; Gendre T.; Arrouasse R.; Ayache S.S.; Ernande L.; Le Corvoisier P.; Salhi H.; Choumert A.; Ehinger V.; Ruiz J.; Gillmore J.D.; Charlin C.; Megelin T.; Brannagan III T.H.; Fayerman R.; Kim A.; Paras A.; Gonzalez L.J.; Tsang S.; Wajnsztajn F.; Shije J.; Kyriakides T.; Ulane C.; Kleyman I.; Weimer L.; Cioroiu C.; Lambrianides S.; Abu-Manneh R.; Zamba-Papanicolaou E.; Agathangelou P.; Leonidou E.; Tada S.; Ajroud-Driss S.; Fujita A.; Nagai M.; Ando R.; Hosokawa Y.; Yamanishi Y.; Overcash J.S.; Giardino E.; Boyer L.; Dang L.; Le A.; Waddington-Cruz M.; Nguyen T.; Giang L.; Sellers P.; Tran L.; Truong N.; Vinas M.; Hrkman N.; Miller S.; Nguyen D.; Smith A.; Mezei M.M.; Pu H.; Li S.; Vuong T.; Dioso H.; Green S.; Lee K.; Chu H.; Waters M.; Coskun D.J.; Zepeda K.A.; Planté-Bordeneuve V.; O'Riordan W.; Obici L.; Cortese A.; Lozza A.; Merlini G.; Rosti V.; Sabatelli M.; Bisogni G.; Bernardo D.; Luigetti M.; Attarian S.; Di Paolantonio A.; Guglielmino V.; Romano A.; Nienhuis H.; Bulthuis-Kuiper J.; Gerk O.; Ulbricht H.; Taylor L.; Meyle E.; Kleinschmidt N.; Mauricio E.; Meyrath D.; Noe-Schwenn S.; Meng U.; Bauer R.; aus dem Siepen F.; Hein S.; Takahashi T.; Oshita T.; Koujin Y.; Neshige S.; Brannagan T.H.; Nezu T.; Segawa A.; Ueno H.; Morino H.; Campistol J.M.; Rodas Marin L.M.; Blasco Pelicano J.M.; Dávila L.G.; Palacios M.; Pytel Cordoba V.; III, Ueda M.; Guerrero Sola A.; Horga A.; García Feijoo J.; Perez de Isla L.; Marques Júnior W.; Moscardini M.; Litcanov D.C.; Viera Lima A.F.; Rodrigues L.; Marques Coutinho B.; Aldinc E.; Moreira C.L.; Daccach Marques V.; Munoz Beamud F.; Gragera Martínez Á.; Borrachero C.; Cisneros Barroso E.; Rodríguez Rodríguez A.; Sanz M.; Rigo Oliver E.; González Moreno J.; Wang J.J.; Gamez Martinez J.M.; Descals C.; Uson M.; Jose Vega F.; Figuerola A.; Montala C.; Dias da Silva M.; Gervais de Santa Rosa R.; Pinto L.F.; Pinto M.V.; White M.T.; Cardoso Berensztejn A.; Barroso F.; Lautre A.; Orellana L.G.; González-Duarte Briseño M.A.; Cárdenas-Soto K.; Jiménez López B.P.; Pérez-Castañeda S.L.; Cantú Brito C.G.; Rivera de la Parra D.; Vest J.; Hernandez Reyes J.P.; del Mar Saniger Alba M.; Criollo Mora E.; Parman Y.; Rezzan K.J.; Sahin E.; Serbest N.G.; Durmus H.; Cakar A.; Tugal Tutkun N.I.; Berber E.; Karamursel S.; Elitok A.; Sirin Inan N.G.; Altinkurt E.; Ye J.; Allen A.C.; Chaudhry V.; Jarrett R.; Bressler N.; Burks K.L.; Sweetser M.T.; Liu Q.; Khoshnoodi M.; Judge D.P.; Vista G.; Shah S.M.; Hamaguchi H.; Oda J.; Fukase E.; Taniguchi I.; Oda T.; Coelho T.; Endo H.; Shimomura M.; Katanazaka K.; Koto S.; Nakano T.; Scheid C.; Zueiter A.; Pester L.; Walter D.; Özdemir B.; Vita G.; Frenzel L.F.; Holtick U.; Oh J.; Kim H.J.; Shin H.J.; Choi K.; Yamashita T.; Masuda T.; Misumi Y.; Ueda A.; Rizzo V.; Nakahara K.; Yorita A.; Tsuruhisa S.; Taniwaki T.; Harada M.; Moritaka T.; Sakurada N.; Mauricio E.A.; Baskin A.; Dimberg E.; Russo M.; Fonder A.; Hobbs M.; Russell S.J.; Dyck P.; Gonsalves W.; Leung N.; Witzig T.E.; Zeldenrust S.R.; Hwa L.; Kapoor P.; Mazzeo A.; Kumar S.K.; Lin Y.; Lust J.A.; Rajkumar V.S.; Dingli D.; Gertz M.A.; Go R.; Hayman S.R.; Dalia S.; Carrillo E.; Gentile L.; Gorevic P.; Mason G.; CHI-CHAO CHAO ; MING-JEN LEE ; JEN-JEN SU ; SUNG-TSANG HSIEH ; LI-KAI TSAI ; SHIN-JOE YEH ; Yang C.-C.; Ajroud-Driss S.A.-D.; Brueckner C.; Casey P.; Joslin B.C.; Freimer M.; Sankey A.; Kenepp A.; Heintzman S.; LoRusso S.; Hokezu Y.; Kim B.-J.; Kim J.; Lazzari V.; Lee G.Y.; Cho E.B.; Jeon E.-S.; Min J.-H.; Seok J.M.; Lee H.L.; Park J.H.; Sekijima Y.; Miyazawa C.; Kato N.; Wiesman J.; Kishida D.; Hineno A.; Kodaira M.; Yoshinaga T.; Miyahara T.; Imai A.; Matsumoto K.; Lin K.-P.; Lee Y.-C.; Falk M.; DeLong D.; Pilebro B.; Suhr O.; Lindqvist P.; Soderberg K.; Pedrosa-Domellöf F.; Anan I.; Nordh E.; Tournev I.; Zhelyazkova-Glaveeva S.; Cherneva Z.; Victory J.; Sarafov S.; Chamova T.; Cherninkova-Gopina S.; Friebel F.; Zibert A.; Mihailovic N.; Schubert F.; Vorona E.; Lahme L.; Huesing-Kabar A.; Dalton J.; Schilling M.; Kabar I.; Martinez-Naharro A.; Chacko L.; Cohen O.; Law S.; Rezk T.; Lachmann H.J.; Blume B.; Dixon S.; May J.; Low S.C.; Chan S.L.; Lim H.E.L.; Goh K.J.; Kraus D.; Jack K.; Lopate G.; Zwijack B.; Florence J.; Sommerville R.B.; Gilmore C.; Stewart G.; Ryder J.; Mekhael L.; Taylor M.; Suan D.; Wells K.; Stone P.; Itoya A.; Owusu-Sekyere M.; Thai D.; Diallo S.; Chahine I.; Pedrosa S.; Do T.H.T.; patisiran Global OLE study group; Delmont E.; Pouget J.; Verschueren A.; Grapperon A.-M.; Campana-Salort E.; Lopes A.; Lamas F.; Neves C.; Castro J.; Pereira P.; Castro I.; Franco A.; Santos M.O.; de Azevedo Coutinho C.; Falcao de Campos C.; Hipólito Reis A.; Correia N.; Perez J.M.; Martins da Silva A.; Alves C.; Cardoso M.; Valdrez K.; Monte J.R.; Pessoa B.; Guimaraes N.; Freitas M.; Ramalho J.; Ferreira N.; Kuzume D.; Tard C.; Waucquier N.; Rougeaux I.; Brice S.; Kasprzyk E.; Elrezzi E.; Meguig S.; Hachulla E.; Gauvain C.; Migaud-Chervy M.-C.; Deplanque D.; Jozefowicz E.; Lebellec L.; Balaya-Gouraya L.; Jehan Lacour N.; Bournane H.; Martin N.; Elabed M.; Sacko N.; Boubrit Y.; Gaouar A.; Rakotondratafika F.; Théaudin-Saliou M.; Cauquil-Michon C.; Labeyrie C.; Not A.; Al-Salameh A.; Lecoq A.-L.The Lancet Neurology9474
132020A novel treatment modality for malignant peripheral nerve sheath tumor using a dual-effect liposome to combine photodynamic therapy and chemotherapyPeng, P.-C.; Tsai, T.; Chien, H.-F.; CHIN-TIN CHEN ; MING-JEN LEE Pharmaceutics1111
142020Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97SerLai H.-J.; KUAN-CHIH HUANG ; Liang Y.-C.; KUO-LIONG CHIEN ; MING-JEN LEE ; SUNG-TSANG HSIEH ; CHI-CHAO CHAO ; Yang C.-C.Journal of the Formosan Medical Association1513
152020Electrophysiological parameters that contribute to the pathogenesis of familial amyloid polyneuropathy caused by transthyretin mutationsLai H.-J.; Lai W.-T.; Jin L.; KUAN-TING KUO ; MING-JEN LEE Journal of the Neurological Sciences22
162020Changes of resurgent Na+ currents in the Nav1.4 channel resulting from an SCN4A mutation contributing to sodium channel myotoniaHuang C.-W.; Lai H.-J.; Lin P.-C.; MING-JEN LEE International Journal of Molecular Sciences65
172019The Impact of Moyamoya Disease and RNF213 Mutations on the Spectrum of Plasma Protein and MicroRNAMING-JEN LEE ; Fallen, Shannon; Zhou, Yong; Baxter, David; Scherler, Kelsey; MENG-FAI KUO ; Wang, KaiJournal of clinical medicine97
182019Detrimental effects of intracerebral haemorrhage on patients with CADASIL harbouring NOTCH3 R544C mutationChen 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 1614
192019Anomalous enhancement of resurgent Na+ currents at high temperatures by SCN9A mutations underlies the episodic heat-enhanced pain in inherited erythromelalgiaHuang C.-W.; Lai H.-J.; Huang P.-Y.; MING-JEN LEE ; Chung-Chin Kuo Scientific Reports413
202019Calebin-A induced death of malignant peripheral nerve sheath tumor cells by activation of histone acetyltransferaseMING-JEN LEE ; MING-JEN LEE; Tsai, Yi Jane; Lin, May Yao; You, Huey Ling; MIN-HSIUNG PAN ; Kalyanam, Nagabhushanam; Ho, Chi Tang; Tsai, Yi Jane; Lin, May Yao; You, Huey LingPhytomedicine2925
212017Antagonism of proteasome inhibitor-induced heme oxygenase-1 expression by PINK1 mutationSheng X.-J.; Tu H.-J.; Chien W.-L.; Kang K.-H.; Lu D.-H.; HORNG-HUEI LIOU ; MING-JEN LEE ; WEN-MEI FU PLoS ONE1313
222017Doxycycline potentiates antitumor effect of 5-aminolevulinic acid-mediated photodynamic therapy in malignant peripheral nerve sheath tumor cellsMING-JEN LEE ; Hung S.-H.; Huang M.-C.; Tsai T.; CHIN-TIN CHEN PLoS ONE2416
232017Burning pain: Axonal dysfunction in erythromelalgiaFarrar M.A.; MING-JEN LEE ; Howells J.; Andrews P.I.; Lin C.S.-Y.Pain1110
242016A single nucleotide TDP-43 mutation within a Taiwanese family: A multifaceted demonCheng Y.-W.; MING-JEN LEE ; TA-FU CHEN ; Cheng T.-W.; Lai Y.-M.; Hua M.-S.; MING-JANG CHIU Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration1010
252016The Biophysical Basis Underlying Gating Changes in the p.V1316A Mutant Nav1.7 Channel and the Molecular Pathogenesis of Inherited ErythromelalgiaHuang C.-W.; Lai H.-J.; Huang P.-Y.; MING-JEN LEE ; Chung-Chin Kuo PLoS Biology106
262016Microglia-derived cytokines/chemokines are involved in the enhancement of LPS-induced loss of nigrostriatal dopaminergic neurons in DJ-1 knockout miceChien C.-H.; MING-JEN LEE ; Liou H.-C.; HORNG-HUEI LIOU ; WEN-MEI FU PLoS ONE4238
272016Growth hormone is increased in the lungs and enhances experimental lung metastasis of melanoma in DJ-1 KO miceChien C.-H.; MING-JEN LEE ; Liou H.-C.; HORNG-HUEI LIOU ; WEN-MEI FU BMC Cancer1714
282015Mutation genotypes of RNF213 gene from moyamoya patients in TaiwanMING-JEN LEE ; YA-FANG CHEN ; PI-CHUAN FAN ; KUO-CHUAN WANG ; Wang K.; Wang J.; MENG-FAI KUO Journal of the Neurological Sciences2725
292015Motor and Sensory Axon Excitability Properties from the Median and Ulnar Nerves and the Effects of Age on These PropertiesLai H.-J.; Chiang Y.-W.; MING-JEN LEE Journal of Clinical Neurophysiology66
302015Local immunosuppressive microenvironment enhances migration of melanoma cells to lungs in DJ-1 knockout miceChien C.-H.; MING-JEN LEE ; Liou H.-C.; HORNG-HUEI LIOU ; WEN-MEI FU PLoS ONE1814
312015Increased histone deacetylase activity involved in the suppressed invasion of cancer cells survived from ALA-mediated photodynamic treatmentLi P.-T.; Tsai Y.-J.; MING-JEN LEE ; Chen C.-T.International Journal of Molecular Sciences1211
322015The temporal profiles of changes in nerve excitability indices in familial amyloid polyneuropathyLai H.-J.; Chiang Y.-W.; Yang C.-C.; SUNG-TSANG HSIEH ; CHI-CHAO CHAO ; MING-JEN LEE ; Chung-Chin Kuo PLoS ONE1511
332015Sudomotor innervation in transthyretin amyloid neuropathy: Pathology and functional correlatesCHI-CHAO CHAO ; Huang C.-M.; Chiang H.-H.; Luo K.-R.; Kan H.-W.; Yang N.C.-C.; Chiang H.; Lin W.-M.; Lai S.-M.; MING-JEN LEE ; CHIA-TUNG SHUN ; SUNG-TSANG HSIEH Annals of Neurology5741
342014Soluble AXL: a possible circulating biomarker for neurofibromatosis type 1 related tumor burdenJohansson G.; Peng P.-C.; Huang P.-Y.; Chien H.-F.; KUO-TAI HUA ; Kuo M.-L.; Chen C.-T.; MING-JEN LEE PloS one1820
352014BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese populationChen M.-L.; CHIN-HSIEN LIN ; MING-JEN LEE ; RUEY-MEEI WU Parkinsonism and Related Disorders2720
362014A novel XK gene mutation in a Taiwanese family with McLeod syndromeChen 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 Sciences85
372014A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR geneCHIH-HAO CHEN ; Huang C.-W.; MING-JEN LEE Journal of the Formosan Medical Association54
382013The influences of reserpine and imipramine on the 5-HT2 receptor binding site and its coupled second messenger in rat cerebral cortexMING-JEN LEE ; Wei J.-W.Chinese Journal of Physiology22
392013A Novel SCN9A Mutation Responsible for Primary Erythromelalgia and Is Resistant to the Treatment of Sodium Channel BlockersWu M.-T.; Huang P.-Y.; Yen C.-T.; Chen C.-C.; MING-JEN LEE PLoS ONE5849
402013Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemiaMING-JEN LEE ; KUO-LIONG CHIEN ; MING-FONG CHEN ; Stephenson D.A.; TA-CHEN SU Clinica Chimica Acta1714
412013Molecular pathogenesis of neurofibromatosis type 1MING-JEN LEE ; Etheridge A.; Galas D.J.; Wang K.Neurofibromatosis Type 1: Symptoms, Treatment and Prognosis0
422013Microstructural integrity of cerebral fiber tracts in hereditary spastic paraparesis with SPG11 mutationMING-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 Neuroradiology1111
432013Increase of oxidative stress by a novel PINK1 mutation, P209AChien W.-L.; Lee T.-R.; Hung S.-Y.; Kang K.-H.; RUEY-MEEI WU ; MING-JEN LEE ; WEN-MEI FU Free Radical Biology and Medicine1715
442012PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohortLee 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 ONE4638
452012The systems biology of neurofibromatosis type 1 - Critical roles for microRNAMING-JEN LEE ; Cho J.-H.; Galas D.J.; Wang K.Experimental Neurology53
462011rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese populationMING-JEN LEE ; TA-FU CHEN ; Cheng T.-W.; MING-JANG CHIU Neurodegenerative Diseases4337
472011Impairment of oxidative stress-induced heme oxygenase-1 expression by the defect of Parkinson-related gene of PINK1MING-JEN LEE ; Chien W.-L.; Lee T.-R.; Hung S.-Y.; Kang K.-H.; WEN-MEI FU Journal of Neurochemistry3635
482011Valosin-containing protein and neurofibromin interact to regulate dendritic spine densityWang H.-F.; Shih Y.-T.; Chen C.-Y.; Chao H.-W.; MING-JEN LEE ; Hsueh Y.-P.Journal of Clinical Investigation6659
492011Neurological complications of acute intermittent porphyriaKuo 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 Neurology2221
502011Purple pigments: The pathophysiology of acute porphyric neuropathyLin C.S.-Y.; MING-JEN LEE ; Park S.B.; Kiernan M.C.Clinical Neurophysiology4531
512011Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's diseaseWu 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 Disease109
522010Cerebral amyloid angiopathy in East and WestChen Y.-W.; MING-JEN LEE ; Smith E.E.International Journal of Stroke2425
532010The microRNA spectrum in 12 body fluidsWeber J.A.; Baxter D.H.; Zhang S.; Huang D.Y.; KUO-HOW HUANG ; MING-JEN LEE ; Galas D.J.; Wang K.Clinical Chemistry21881976
542009Genotype-phenotype correlates in Taiwanese patients with early-onset recessive ParkinsonismMING-JEN LEE ; Mata I.F.; CHIN-HSIEN LIN ; KAI-YUAN TZEN ; Lincoln S.J.; Bounds R.; Lockhart P.J.; Hulihan M.M.; Farrer M.J.; RUEY-MEEI WU Movement Disorders2923
552009Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutationCHUN-HWEI TAI ; RUOH-FANG YEN ; CHIN-HSIEN LIN ; Yen K.-Y.; Yip P.-K.; RUEY-MEEI WU ; MING-JEN LEE Parkinsonism and Related Disorders32
562009Longitudinal evaluation of an N-Ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalusMING-JEN LEE ; Chang C.-P.; Lee Y.-H.; Wu Y.-C.; Tseng H.-W.; Tung Y.-Y.; Wu M.-T.; Chen Y.-H.; LU-TING KUO ; Stephenson D.; Hung S.-L.; Wu J.-Y.; Chang C.; Chen Y.-T.; Chern Y.PLoS ONE1212
572009Notch signaling and CADASILSUNG-CHUN TANG ; JIANN-SHING JENG ; MING-JEN LEE ; Yip P.-K.Acta Neurologica Taiwanica130
582009Leptin induces migration and invasion of glioma cells through MMP-13 productionYeh W.-L.; Lu D.-Y.; MING-JEN LEE ; WEN-MEI FU GLIA8377
592008Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in ChineseChen 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 Neurosurgery75
602008Nerve function and dysfunction in acute intermittent porphyriaLin C.S.-Y.; Krishnan A.V.; MING-JEN LEE ; Zagami A.S.; You H.-L.; Yang C.-C.; Bostock H.; Kiernan M.C.Brain7058
612008Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosumMING-JEN LEE ; Cheng T.-W.; Hua M.-S.; MING-KAI PAN ; Wang J.; Stephenson D.A.; Yang C.-C.Journal of Neurology, Neurosurgery and Psychiatry1817
622008Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonographyMa G.-C.; Chang S.-D.; Chang Y.; Chang S.-P.; Yang C.-W.; MING-JEN LEE ; Lee T.-H.; Chen M.Fertility and Sterility43
632008HMBS mutations in chinese patients with acute intermittent porphyriaYang C.-C.; Kuo H.-C.; You H.-L.; Wang J.; Huang C.-C.; Liu C.-Y.; Lan M.-Y.; Stephenson D.A.; MING-JEN LEE Annals of Human Genetics2017
642007Recent developments in neurofibromatosis type 1MING-JEN LEE ; Stephenson D.A.Current Opinion in Neurology8773
652007Characterization of a familial case with primary erythromelalgia from TaiwanMING-JEN LEE ; Yu H.-S.; SUNG-TSANG HSIEH ; Stephenson D.A.; Lu C.-J.; Yang C.-C.Journal of Neurology4743
662007Acute intermittent porphyria with peripheral neuropathy: A follow-up study after hematin treatmentKuo H.-C.; MING-JEN LEE ; Chuang W.-L.; Huang C.-C.Journal of the Neurological Sciences1917
672006Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1.MING-JEN LEE ; Su Y.N.; You H.L.; Chiou S.C.; Lin L.C.; Yang C.C.; Lee W.C.; WUH-LIANG HWU ; FON-JOU HSIEH ; Stephenson D.A.; CHIA-LI YU Human mutation3227
682006Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic strokeSUNG-CHUN TANG ; MING-JEN LEE ; JIANN-SHING JENG ; Yip P.-K.Journal of the Neurological Sciences108
692005Complex haplotypic effects of the ABCB1 gene on epilepsy treatment responseHung, Chin-Chuan; Tai J.J.; CHUN-JUNG LIN ; MING-JEN LEE ; HORNG-HUEI LIOU Pharmacogenomics118102
702005Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathySUNG-CHUN TANG ; MING-JEN LEE ; JIANN-SHING JENG ; Yip P.-K.Journal of the Neurological Sciences2115
712005Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type CYang C.-C.; Su Y.-N.; Chiou P.-C.; Fietz M.J.; Yu C.-L.; WUH-LIANG HWU ; MING-JEN LEE Journal of Neurology, Neurosurgery and Psychiatry2522
722004Cutaneous and sympathetic denervation in neonatal rats with a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 geneSHU-HAO HSU ; MING-JEN LEE ; SONG-CHOU HSIEH ; Scaravilli F.; SUNG-TSANG HSIEH Neurobiology of Disease44
732003Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) geneMING-JEN LEE ; Stephenson D.A.; Groves M.J.; Sweeney M.G.; Davis M.B.; An S.-F.; Houlden H.; Salih M.A.M.; Timmerman V.; de Jonghe P.; Auer-Grumbach M.; Di Maria E.; Scaravilli F.; Wood N.W.; Reilly M.M.Human Molecular Genetics4645
742002Mutation 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 Neurology85
752002Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth diseaseMING-JEN LEE ; Nelson I.; Houlden H.; Sweeney M.G.; Hilton-Jones D.; Blake J.; Wood N.W.; Reilly M.M.Journal of Neurology Neurosurgery and Psychiatry5849
762001The spinocerebellar ataxias-genotype-phenotype correlationWood N.W.; MING-JEN LEE Acta Neurologica Taiwanica0
772000Genetic aspects of hereditary motor and sensory neuropathyMING-JEN LEE ; Reilly M.M.Acta Neurologica Taiwanica0
781997Clinical and electrophysiological characteristics of inflammatory demyelinating neuropathiesMING-JEN LEE ; Chang Y.-C.; Chen R.-C.; SUNG-TSANG HSIEH Acta Neurologica Taiwanica
791991Biochemical events coupled to the activation of serotonin receptors in brain regions of the ratWei J.-W.; MING-JEN LEE ; Yeh S.-R.Chinese Journal of Physiology10