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同卵双生多巴反应性肌张力障碍2例并临床分析 被引量:2

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出处 《卒中与神经疾病》 2009年第3期183-183,共1页 Stroke and Nervous Diseases
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  • 1Segawa M,Hosaka A,Miyagawa F,et al.Hereditary progressive dystonia with marked diurnal fluctuation.Adv Neurol,1976,14:215-233.
  • 2Ichinose H,Ohye T,Takahashi E,et al.Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the CTP cyclohydrolase I gene.Nat Genet,1994,8:236-242.
  • 3Jan MM.Misdiagnoses in children with dopa-responsive dystonia.Pediatr Neurol,2004,31:298-303.
  • 4Winkler AS,Reuter I,Harwood C,et al.The frequency and significance of 'striatal toe' in parkinsonism.Parkinsonism Relat Disord,2002,9:97-101.
  • 5Segawa M,Nomura Y,Nishiyama N.Autosomal dominant guanosine triphosphate cyclohydrolase Ⅰ deficiency (Segawa disease).Ann Neurol,2003,54:S32-45.
  • 6Segawa M,Nomura Y.Hereditary progressive dystonia with marked diurnal fluctuation.Pathophysiological importance of the age of onset.Adv Neurol,1993,60:568-576.
  • 7Hwang WJ,Calne DB,Tsui JK,et al.The long-term response to levodopa in dopa-responsive dystonia.Parkinsonism Relat Disord,2001,8:1-5.
  • 8陈蕾,张本恕,孙峰,赵鹏,肖颖.多巴反应性肌张力障碍的临床特点和基因诊断[J].中华神经科杂志,2008,41(11):756-759. 被引量:5
  • 9利婧,胡朝晖,喻长顺,操基清,杨娟,李亚勤,詹益鑫,张成.多巴反应性肌张力障碍长期随访四例[J].中华神经科杂志,2013,46(3):153-158. 被引量:11

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