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

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Showing items 11-20 of 123 (13 Page(s) Totally)
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Institution	Date	Title	Author
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.

Showing items 11-20 of 123 (13 Page(s) Totally)
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