Parkinsonism

  • 网络帕金森病;帕金森氏症;帕金森症;帕金森综合征;帕金森综合症
ParkinsonismParkinsonism
  1. To study effective method for disordered sports of parkinsonism .

    探讨提高帕金森病运动障碍的有效办法。

  2. Mirror movements in parkinsonism : Evaluation of a new clinical sign

    帕金森综合征患者的镜像运动:对一个新临床体征的评价

  3. The clinical analysis of 60 patients with juvenile parkinsonism

    青少年型帕金森病60例临床分析

  4. Parkinsonism Model and Cell Transplantation Treatment in Rhesus Monkeys : MRI Evaluation

    MRI对于恒河猴PD模型建立和治疗的评价

  5. A Clinical Analysis of 58 Patients with Parkinsonism Syndrome Secondary to Carbon Monoxide Poisoning

    CO中毒继发帕金森综合征58例临床分析

  6. Methods Clinical data of 58 patients with Parkinsonism syndrome and 34 patients with PD were respectively analyzed .

    方法对58例CO中毒后继发帕金森综合征患者的临床资料进行分析,并与34例原发性帕金森病临床资料作对照。

  7. Contrasting clinical and imaging analysis of vascular parkinsonism

    血管性帕金森综合征的临床与影像学分析

  8. Changes of extracellular excitatory amino acid in monkey models of parkinsonism

    帕金森病模型猴细胞外液兴奋性氨基酸含量变化

  9. The clinical and genetic characteristics of autosomal recessive juvenile Parkinsonism in a Chinese family

    青少年型帕金森综合征一个家系的临床及遗传学分析

  10. Intracephalic Transplantation of Adrenal Medulla Improve Parkinsonism ⅰ . Basic Experimental Study

    肾上腺髓质脑内移植治疗震颤麻痹Ⅰ.基础实验研究

  11. Clinical Study of Cervical Ganglion Autograft into Caudate Nucleus in Treatment of Parkinsonism

    自体颈神经节立体定向脑内尾状核移植治疗帕金森氏病的临床研究

  12. Mutation analysis of genes associated with autosomal recessive in early - onset parkinsonism

    常染色体隐性遗传早发性帕金森综合征致病基因的突变分析

  13. Results : The appropriate nursing plan has been developed , and the life of patients with Parkinsonism has been improved .

    结果制定了适合帕金森病人的护理方案,提高了帕金森病人的生活质量。

  14. Clinical Characteristics of Vascular Parkinsonism

    血管性帕金森综合征临床特点的分析

  15. The application of stellate ganglion block during the recovery of dysphagia of parkinsonism patients

    星状神经节阻滞在帕金森病吞咽障碍康复中的应用

  16. Genotype and phenotype analyses of three families with autosomal recessive juvenile parkinsonism

    三个常染色体隐性遗传性青少年型帕金森综合征家系的基因型与表型分析

  17. Patients with drug-induced or vascular parkinsonism or dementia were excluded .

    那些药物诱导或痴呆的病人已经被排除。

  18. The experimental study on the activity of striatal dopamine D_2 receptor in parkinsonism monkey model

    帕金森病猴模型纹状体多巴胺D2受体的显像研究

  19. Objective To investigate the clinical features of Parkinsonism syndrome secondary to carbon monoxide poisoning and Parkinson 's disease .

    目的探讨CO中毒继发帕金森综合征的临床特点,并与原发帕金森病鉴别。

  20. Fluctuating cognitive impairment , visual hallucination , and Parkinsonism are all its clinical characteristics .

    以波动性认知功能障碍、视幻觉和帕金森病综合征为路易体痴呆的特征性临床特点。

  21. Exon rearrangement analysis of parkin gene in patients with isolated early-onset parkinsonism using semi-quantitative PCR

    荧光半定量PCR在散发早发性帕金森综合征parkin基因外显子重排突变分析中的应用

  22. Cardiac ~ ( 123 ) I-MIBG scintigraphy in patients with drug induced parkinsonism

    药物诱导帕金森病患者的心肌~(123)I-MIBG闪烁扫描检查

  23. Association Analysis of the Parkin Gene and Mutation Screening in Sporadic Parkinson 's Disease Patients and Family Parkinsonism Patients

    帕金森病Parkin基因多态性的关联研究及早发性和家族性帕金森综合征患者Parkin基因的突变筛查

  24. Up-regulation and aggregation of α - synuclein in mouse model of parkinsonism

    帕金森病模型鼠黑质α-突触核蛋白表达升高并集聚

  25. Effects of Pramipexole Hydrochloride combined with Madopar in the therapy of vascular parkinsonism

    盐酸普拉克索联合美多巴治疗血管性帕金森病的疗效观察

  26. Parkinsonism , premature menopause , and mitochondrial DNA polymerase γ . mutations : Clinical and molecular genetic study

    帕金森病、绝经期提前与线粒体DNA聚合酶γ突变:临床及分子遗传学研究

  27. Transplantation of Fetal Adrenal Medullary Tissue Cultured to the Head of Caudate Nucleus In Parkinsonism

    胎儿肾上腺髓质组织培养立体定向脑内尾状核头部移植治疗震颤麻痹初步临床报告

  28. 33 cases of Vascular Parkinsonism

    血管性帕金森综合征33例

  29. Parkin is a causative gene of autosomal recessive juvenile parkinsonism .

    Parkin是隐性遗传性少年型帕金森病的致病基因。

  30. Conclusion The early differential diagnosis of juvenile parkinsonism in the pedigree should be carried out to direct gene therapy of the disease .

    结论对青年型家族性帕金森综合征应早期鉴别诊断,指导该病的临床及基因治疗。