公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
2006 | 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.; WUH-LIANG HWU ; FON-JOU HSIEH ; Stephenson D.A.; CHIA-LI YU | Human mutation | 32 | 27 | |
2008 | 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.; MING-KAI PAN ; Wang J.; Stephenson D.A.; Yang C.-C. | Journal of Neurology, Neurosurgery and Psychiatry | 18 | 17 | |
2013 | Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemia | MING-JEN LEE ; KUO-LIONG CHIEN ; MING-FONG CHEN ; Stephenson D.A.; TA-CHEN SU | Clinica Chimica Acta | 17 | 14 | |
2007 | Recent developments in neurofibromatosis type 1 | MING-JEN LEE ; Stephenson D.A. | Current Opinion in Neurology | 87 | 73 |