Titlebook: Chorea; Causes and Managemen Federico E. Micheli,Peter A. LeWitt Book 2014 Springer-Verlag London 2014 chorea.choreiform disorder.cognitive

radionuclides

书目名称Chorea影响因子(影响力)




书目名称Chorea影响因子(影响力)学科排名




书目名称Chorea网络公开度




书目名称Chorea网络公开度学科排名




书目名称Chorea被引频次




书目名称Chorea被引频次学科排名




书目名称Chorea年度引用




书目名称Chorea年度引用学科排名




书目名称Chorea读者反馈




书目名称Chorea读者反馈学科排名

闷热

obnoxious

强制性

,Sydenham’s Chorea, its declining prevalence (particularly in developed countries), it is the most common explanation for acute onset of chorea in children. It is more common in girls than boys, and its features include chorea, decreased muscle tone, tics, and nonmovement disorder findings such as behavioral abnormali

Repetitions

,Huntington’s Disease: Clinical Phenotypes and Therapeutics,rder. However, using disease models, and studies in human patients, great progress has been made in understanding the pathophysiology of HD. Research has led to the development of the first gene therapy approaches with promising results in HD model systems. This raises hopes that HD, a monogenetic f

dissent

dissent

Huntington Disease and Huntington Disease-Like Syndromes: An Overview,on disease (HD). In addition there are disorders mimicking HD, the so-called HD-like syndromes, and molecular workup revealed that they account for about 1 % of suspected HD cases. The aim of this review is to summarize the main characteristics of these rare conditions in order to familiarize clinic

chance

McLeod Syndrome,is and progressive striatal neurodegeneration. The so-called core NA syndromes include autosomal recessive chorea-acanthocytosis and X-linked McLeod syndrome. These two disorders have a Huntington disease-like phenotype consisting of a hyperkinetic, mostly choreatic, movement disorders, psychiatric

anagen

Cardioversion