第 1 到 5 筆結果,共 5 筆。
公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 | |
---|---|---|---|---|---|---|---|
1 | 2009 | Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation | CHUN-HWEI TAI ; RUOH-FANG YEN ; CHIN-HSIEN LIN ; Yen K.-Y.; Yip P.-K.; RUEY-MEEI WU ; MING-JEN LEE | Parkinsonism and Related Disorders | 3 | 2 | |
2 | 2009 | Notch signaling and CADASIL | SUNG-CHUN TANG ; JIANN-SHING JENG ; MING-JEN LEE ; Yip P.-K. | Acta Neurologica Taiwanica | 13 | 0 | |
3 | 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 | |
4 | 2005 | Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy | SUNG-CHUN TANG ; MING-JEN LEE ; JIANN-SHING JENG ; Yip P.-K. | Journal of the Neurological Sciences | 21 | 15 | |
5 | 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 |