1) progressive bulbar paralysis
进行性延髓麻痹
2) progressive bulbar paralysis
进行性延髓性麻痹
4) bulbar paralysis
延髓麻痹
1.
Most of them had dizziness,nausea and vomiting at the early stage of onset and their principal symptoms were bulbar paralysis and sensory disturbance.
结果:12例患者均为梗死所致,以眩晕、恶心、呕吐起病者多,延髓麻痹和感觉障碍为主要表现,头部MRI阳性率100%,经治疗眩晕、恶心、呕吐、声音嘶哑及吞咽困难恢复较快,感觉障碍恢复最慢。
2.
Objective: Approach the traditional Chinese medicine pathogenesis of amyotrophic lateral sclerosis(ALS) directed by Qi-jing and Collateral disease theory , observe and evaluate the clinical curative effect of JIWEILING injection (JWL) which is made directed by these theory in dealing with amyotrophic lateral sclerosis(ALS) bulbar paralysis.
目的:通过研究在奇经、络病理论指导下治疗肌萎缩侧索硬化症(Amyotrophic lateral sclerosis,ALS)延髓麻痹的中医机理,观察并评价在该理论指导下研制的肌萎灵注射液对ALS延髓麻痹的临床疗效,从而为临床上验证新药的确切疗效提供可靠的依据。
3.
Bulbar paralysis is a common stubborn and severe disease in department of neurology, including true paralysis and pseudoparalysis.
延髓麻痹包括真性延髓麻痹和假性延髓麻痹,是神经科常见的疑难危重症。
5) Pseudobulbar palsy
假性延髓麻痹
1.
Study of nape needle acupuncture therapy on pseudobulbar palsy
环颈七针治疗假性延髓麻痹的临床研究
6) progressive paralysis
进行性麻痹
补充资料：低血钾性周期性麻痹
低血钾性周期性麻痹
hypokalemic periodic paralysis
家族性周期性麻痹中的一种类型。为常染色体显性遗传。在我国大多数病例为散发而无家族史。发作多在夜间或清晨醒来时，病儿发觉不能移动自己的肢体，但说话和呼吸正常，重症四肢完全不能活动，不能抬头。发作时肌肉呈弛缓性麻痹，腱反射消失，感觉正常。麻痹持续数小时至2天。发作频度不等，一般不多于每月1次。发作时血清钾减低，为2.5～3.5mmol/L，心电图有低血钾表现。治疗发作时给一次氯化钾口服；重者可静脉滴注氯化钾，同时心电监护以防高钾血症。预防发作可于每晚睡前服氯化钾一次。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条