臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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机构	日期	题名	作者
臺大學術典藏	2020-03-03T02:33:37Z	Clinical and electrophysiological characteristics of inflammatory demyelinating neuropathies	MING-JEN LEE; Chang Y.-C.; Chen R.-C.; Hsieh S.-T.
臺大學術典藏	2020-03-03T02:33:37Z	Biochemical events coupled to the activation of serotonin receptors in brain regions of the rat	Wei J.-W.; MING-JEN LEE; Yeh S.-R.
臺大學術典藏	2020-03-03T02:33:36Z	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.
臺大學術典藏	2020-03-03T02:33:36Z	Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene	MING-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.
臺大學術典藏	2020-03-03T02:33:36Z	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.
臺大學術典藏	2020-03-03T02:33:36Z	Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease	MING-JEN LEE; Nelson I.; Houlden H.; Sweeney M.G.; Hilton-Jones D.; Blake J.; Wood N.W.; Reilly M.M.
臺大學術典藏	2020-03-03T02:33:36Z	The spinocerebellar ataxias-genotype-phenotype correlation	Wood N.W.; MING-JEN LEE
臺大學術典藏	2020-03-03T02:33:35Z	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.
臺大學術典藏	2020-03-03T02:33:35Z	Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke	Tang S.-C.; MING-JEN LEE; Jeng J.-S.; Yip P.-K.
臺大學術典藏	2020-03-03T02:33:35Z	Identification 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.; Hwu W.L.; Hsieh F.J.; Stephenson D.A.; Yu C.L.
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.

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