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

radionuclides

書目名稱Chorea影響因子(影響力)




書目名稱Chorea影響因子(影響力)學(xué)科排名




書目名稱Chorea網(wǎng)絡(luò)公開度




書目名稱Chorea網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Chorea被引頻次




書目名稱Chorea被引頻次學(xué)科排名




書目名稱Chorea年度引用




書目名稱Chorea年度引用學(xué)科排名




書目名稱Chorea讀者反饋




書目名稱Chorea讀者反饋學(xué)科排名

悶熱

obnoxious

強(qiáng)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