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Institution	Date	Title	Author
臺大學術典藏	2020-03-03T02:33:35Z	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.
臺大學術典藏	2020-03-03T02:33:35Z	Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C	Yang C.-C.; Su Y.-N.; Chiou P.-C.; Fietz M.J.; Yu C.-L.; Hwu W.-L.; MING-JEN LEE
臺大學術典藏	2020-03-03T02:33:35Z	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.
臺大學術典藏	2020-03-03T02:33:34Z	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.; Pan M.-K.; Wang J.; Stephenson D.A.; Yang C.-C.
臺大學術典藏	2020-03-03T02:33:34Z	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.
臺大學術典藏	2020-03-03T02:33:34Z	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.
臺大學術典藏	2020-03-03T02:33:34Z	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.
臺大學術典藏	2020-03-03T02:33:34Z	Recent developments in neurofibromatosis type 1	MING-JEN LEE; Stephenson D.A.
臺大學術典藏	2020-03-03T02:33:33Z	Leptin induces migration and invasion of glioma cells through MMP-13 production	Yeh W.-L.; Lu D.-Y.; MING-JEN LEE; Fu W.-M.
臺大學術典藏	2020-03-03T02:33:33Z	Notch signaling and CADASIL	Tang S.-C.; Jeng J.-S.; MING-JEN LEE; Yip P.-K.
臺大學術典藏	2020-03-03T02:33:33Z	Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism	MING-JEN LEE; Mata I.F.; Lin C.-H.; Tzen K.-Y.; Lincoln S.J.; Bounds R.; Lockhart P.J.; Hulihan M.M.; Farrer M.J.; Wu R.-M.
臺大學術典藏	2020-03-03T02:33:33Z	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.
臺大學術典藏	2020-03-03T02:33:33Z	HMBS mutations in chinese patients with acute intermittent porphyria	Yang 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
臺大學術典藏	2020-03-03T02:33:32Z	Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation	Tai C.-H.; Yen R.-F.; Lin C.-H.; Yen K.-Y.; Yip P.-K.; Wu R.-M.; MING-JEN LEE
臺大學術典藏	2020-03-03T02:33:32Z	Cerebral amyloid angiopathy in East and West	Chen Y.-W.; MING-JEN LEE; Smith E.E.
臺大學術典藏	2020-03-03T02:33:32Z	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.
臺大學術典藏	2020-03-03T02:33:32Z	Longitudinal evaluation of an N-Ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus	MING-JEN LEE; Chang C.-P.; Lee Y.-H.; Wu Y.-C.; Tseng H.-W.; Tung Y.-Y.; Wu M.-T.; Chen Y.-H.; Kuo L.-T.; Stephenson D.; Hung S.-L.; Wu J.-Y.; Chang C.; Chen Y.-T.; Chern Y.
臺大學術典藏	2020-03-03T02:33:31Z	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.
臺大學術典藏	2020-03-03T02:33:31Z	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.
臺大學術典藏	2020-03-03T02:33:31Z	rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population	MING-JEN LEE; Chen T.-F.; Cheng T.-W.; Chiu M.-J.
臺大學術典藏	2020-03-03T02:33:31Z	Impairment of oxidative stress-induced heme oxygenase-1 expression by the defect of Parkinson-related gene of PINK1	MING-JEN LEE; Chien W.-L.; Lee T.-R.; Hung S.-Y.; Kang K.-H.; Fu W.-M.
臺大學術典藏	2020-03-03T02:33:31Z	The microRNA spectrum in 12 body fluids	Weber J.A.; Baxter D.H.; Zhang S.; Huang D.Y.; Huang K.H.; MING-JEN LEE; Galas D.J.; Wang K.
臺大學術典藏	2020-03-03T02:33:30Z	The influences of reserpine and imipramine on the 5-HT2 receptor binding site and its coupled second messenger in rat cerebral cortex	MING-JEN LEE; Wei J.-W.
臺大學術典藏	2020-03-03T02:33:30Z	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.
臺大學術典藏	2020-03-03T02:33:30Z	The systems biology of neurofibromatosis type 1 - Critical roles for microRNA	MING-JEN LEE; Cho J.-H.; Galas D.J.; Wang K.

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