Lee MJ - Search Results

1

Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene.

Lee MJ, Stephenson DA, Groves MJ, Sweeney MG, Davis MB, An SF, Houlden H, Salih MA, Timmerman V, de Jonghe P, Auer-Grumbach M, Di Maria E, Scaravilli F, Wood NW, Reilly MM. Lee MJ, et al. Hum Mol Genet. 2003 Aug 1;12(15):1917-25. doi: 10.1093/hmg/ddg198. Hum Mol Genet. 2003. PMID: 12874111

2

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 SH, Lee MJ, Hsieh SC, Scaravilli F, Hsieh ST. Hsu SH, et al. Among authors: lee mj. Neurobiol Dis. 2004 Jul;16(2):335-45. doi: 10.1016/j.nbd.2004.03.003. Neurobiol Dis. 2004. PMID: 15193290

3

Characterization of a familial case with primary erythromelalgia from Taiwan.

Lee MJ, Yu HS, Hsieh ST, Stephenson DA, Lu CJ, Yang CC. Lee MJ, et al. J Neurol. 2007 Feb;254(2):210-4. doi: 10.1007/s00415-006-0328-3. Epub 2007 Feb 8. J Neurol. 2007. PMID: 17294067

4

Recent developments in neurofibromatosis type 1.

Lee MJ, Stephenson DA. Lee MJ, et al. Curr Opin Neurol. 2007 Apr;20(2):135-41. doi: 10.1097/WCO.0b013e3280895da8. Curr Opin Neurol. 2007. PMID: 17351482 Review.

5

Mutation of the sterol 27-hydroxylase gene ( CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis.

Lee MJ, Huang YC, Sweeney MG, Wood NW, Reilly MM, Yip PK. Lee MJ, et al. J Neurol. 2002 Sep;249(9):1311-2. doi: 10.1007/s00415-002-0762-9. J Neurol. 2002. PMID: 12242561 No abstract available.

6

Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemia.

Lee MJ, Chien KL, Chen MF, Stephenson DA, Su TC. Lee MJ, et al. Clin Chim Acta. 2013 Feb 1;416:31-5. doi: 10.1016/j.cca.2012.10.054. Epub 2012 Nov 23. Clin Chim Acta. 2013. PMID: 23178747

7

Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1.

Lee MJ, Su YN, You HL, Chiou SC, Lin LC, Yang CC, Lee WC, Hwu WL, Hsieh FJ, Stephenson DA, Yu CL. Lee MJ, et al. Among authors: lee wc. Hum Mutat. 2006 Aug;27(8):832. doi: 10.1002/humu.9446. Hum Mutat. 2006. PMID: 16835897

8

Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus.

Lee MJ, Chang CP, Lee YH, Wu YC, Tseng HW, Tung YY, Wu MT, Chen YH, Kuo LT, Stephenson D, Hung SI, Wu JY, Chang C, Chen YT, Chern Y. Lee MJ, et al. Among authors: lee yh. PLoS One. 2009 Nov 17;4(11):e7868. doi: 10.1371/journal.pone.0007868. PLoS One. 2009. PMID: 19924295 Free PMC article.

9

Acute intermittent porphyria with peripheral neuropathy: a follow-up study after hematin treatment.

Kuo HC, Lee MJ, Chuang WL, Huang CC. Kuo HC, et al. Among authors: lee mj. J Neurol Sci. 2007 Sep 15;260(1-2):231-5. doi: 10.1016/j.jns.2007.03.018. Epub 2007 Apr 24. J Neurol Sci. 2007. PMID: 17459418

10

Antagonism of proteasome inhibitor-induced heme oxygenase-1 expression by PINK1 mutation.

Sheng XJ, Tu HJ, Chien WL, Kang KH, Lu DH, Liou HH, Lee MJ, Fu WM. Sheng XJ, et al. Among authors: lee mj. PLoS One. 2017 Aug 14;12(8):e0183076. doi: 10.1371/journal.pone.0183076. eCollection 2017. PLoS One. 2017. PMID: 28806787 Free PMC article.

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