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发作性运动障碍的临床与遗传学 被引量:1

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摘要 发作性运动障碍(Paroxysmal dyskinesias)是一组以反复发作的短暂运动障碍为特征的疾病,具有遗传和临床表现异质性[1].早期报道以家族性较多见,现在散发病例的报道也日渐增多.
出处 《卒中与神经疾病》 2003年第5期320-320,F003,共2页 Stroke and Nervous Diseases
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  • 1Bhatia KP. Familial (idiopathic) paroxysmal dyskinesias: an update.Semin Neurol, 2001, 21(1):69.
  • 2Houser MK, Soland VL, Bhatia KP, et al. Paroxysmal kinesigenic choreoathetosis: a report of 26 patients J Neurol, 1999,246(2) : 120.
  • 3Nagamitsu S, matsuishi T, Hashimoto K, et al. Multicenter study of paroxysmal dyskinesias in Japan-clinical and pedigree analysis.Mov Disord, 1999, 14(4):658.
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  • 8Grunder S, Geisler HS, Rainier S, et al. Acid-sensing ion channel(ASIC) 4 gene: physical mapping, genomic organisation, and evaluation as a candidate for paroxysmal dystonia. Eur J hum Genet,2001, 9(9) :672.
  • 9Munchau A, Valente EM, Shahidi GA, et al. A new family with paroxysmal exercise induced dystonia and migraine a clinical and genetic study. J Neurol Neurosurg Psychiatry, 2000, 68(5):609.
  • 10Pemiola T, Margari L, De laco MG, et al. Familial paroxysmal exercise-induced dyskinesia, epilepsy, and mental retaration in a family with autosomal dominant inheritance. Mov Disord, 2001, 16 ( 4 ) :724.

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