1. |
Nagamitsu S, Matsuishi T, Hashimoto K, et al. Multicenter studyof paroxysmal dyskinesias in Japan:clinical and pedigree analysis[J]. Mov Disord, 1999, 14(4):658-663.
|
2. |
O'Riordan S, Raymond D, Lynch T, et al. Age at onset as a factorin determining the phenotype of primary torsion dystonia[J]. Neurology, 2004, 63(8):1423-1426.
|
3. |
张丽萍, 陈眉, 黄晓明, 等. 发作性运动诱发性舞蹈指痉症国内文献报道216例分析[J].中国神经精神疾病杂志, 2007, 33(10):617-619.
|
4. |
唐宇凤, 周东, 林旭, 等. 发作性运动诱发肌张力障碍的临床与视频脑电图研究[J]. 现代预防医学, 2007, 34(4):881-882.
|
5. |
黄远桂, 黄旌, 陈云春, 等. 41例发作性运动诱发性运动障碍临床与神经电生理分析[J]. 中国神经精神疾病杂志, 2004, 30(3):181-189.
|
6. |
LeDoux MS. The genetics of dystonias[J]. Adv Genet, 2012, 79:35-85.
|
7. |
Wider C, Melquist S, Hauf M, et al. Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1:redefining DYT14 as DYT5[J]. Neurology, 2008, 70(16 Pt2):1377-1383.
|
8. |
Li HF, Chen WJ, Ni W, et al. PRRT2 mutation correlated with phenotypeof paroxysmal kinesigenic dyskinesia and drug response[J]. Neurology, 2013, 80(16):1534-1535.
|
9. |
Chen WJ, Lin Y, Xiong ZQ, et al. Exome sequencing identifies truncatingmutations in PRRT2 that cause paroxysmal kinesigenicdyskinesia[J]. Nat Genet, 2011, 43(12):1252-1255.
|
10. |
中华医学会神经病学分会帕金森病及运动障碍学组. 肌张力障碍诊断与治疗指南[J]. 中华神经科杂志, 2008, 41(8):570-573.
|