Objective To explore the effect of spinal nerve injury on changes of F wave.

The animal model of chronic compressive injury of spinal nerve roots

神经根慢性嵌压损伤的动物模型建立

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Experimental study of protective effect of local infiltration of methylprednisolone on injured spinal nerve root

甲基强地松龙局部浸润对脊神经根炎性损伤后影响的实验研究

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Methods The spinal nerve roots were injured in 20 rabbits.

方法20只家兔全部制成脊神经根炎性损伤的动物模型并饲养3d。

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Because they do spinal with only a25G needle, which is so slim that even puncture of vessel doesn't result in much bleeding.

硬膜外针很粗加上置管的损伤，出血较多且很难避免，因此不作硬膜外是有道理的。

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Clinical observation of implantation tube by stage for treating lacrimal canalicular laceration. Double spinal needle probing method in the management of old laceration of lacrimal canaliculus

泪小管断裂分期置管的临床观察双腰穿针法治疗陈旧性泪小管断裂

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Objective To introduce a double spinal needle probing method in the management of old laceration of lacrimal canaliculus.

目的介绍双腰穿针法治疗陈旧性泪小管断裂。方法第一根腰穿针经上泪点泪道探通，并以其为支撑行泪总管或泪囊切开。

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Fourteen cases of old laceration of lacrimal canaliculus were treated with double spinal needle probing method.

用双腰穿针法治疗陈旧性泪小管断离14例。

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ATP staining revealed isotype muscle grouping and muscle fibre compensative hypertrophy. CONCLUSION: Muscle biopsy has significances in diagnosis and differentiation of adult spinal muscular atrophy.

结论：肌活检对成人型脊髓性肌萎缩症具有诊断和鉴别诊断意义。

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Methods: we used deidentified, family-reported data from participants in the international spinal muscular atrophy patient registry and obtained additional clinical information through a mail-in questionnaire.

方法：应用来源于国际脊肌萎缩症患者注册处的鉴定、家庭报道数据，并通过邮寄问卷的形式获得更多的临床信息。

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Objective To investigate the relationship between survival motor neuron ( SMN) gene and the clinical features of childhood spinal muscular atrophy ( SMA).

目的探讨运动神经元存活基因与儿童期脊肌萎缩症临床特征的关系。

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By segregation analysis of recessive inheritance, 23 cases of 12 pedigree suffering from spinal muscular atrophy fit autosomal recessive inheritance.

隐性遗传分离分析表明，12个家系23例患儿发病方式符合常染色体隐性遗传。

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The clinicopathological changes were investigated by electromyogram ( EMG) and muscle biopsy in 30 cases of chronic spinal muscular atrophy.

对30例慢性肌脊髓性萎缩症患者进行肌电图和肌活检检查。

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Spinal muscular atrophy in childhood is one of the most common neuromuscular disorders with an autosomal recessive mode of inheritance.

儿童型脊髓性肌萎缩症是常见的遗传性神经肌肉病，为常染色体隐性遗传。

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Progressive spinal muscular atrophy

脊髓性进行性肌萎缩

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In humans, probably the most common genetic disorder caused by inbreeding is spinal muscular atrophy ( SMA).

在人类中，由近亲繁殖带来的最普遍的遗传缺陷可能是脊髓性肌肉萎缩症。

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Objective To carry out prenatal gene diagnosis in a pedigree of infantile spinal muscular atrophy ( SMA).

目的对一婴儿型脊肌萎缩症家系进行产前基因诊断。

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Objective To investigate the clinical and electrophysiology features of infantile spinal muscular atrophy, and explore the clinical significance of genetic diagnosis.

目的探讨婴儿型脊髓性肌萎缩症的临床、电生理特点及基因诊断的临床意义。

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Detection of SMN gene deletions in spinal muscular atrophy

脊肌萎缩症基因缺失的初步研究

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Analysis of clinical manifestation and EMG in patients with spinal muscular atrophy accompanied by elevation of CK levels

肌酸磷酸激酶增高的脊髓性肌萎缩症患者临床与肌电图分析

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Study of NAIP gene in spinal muscular atrophy

脊髓性肌萎缩患儿的NAIP基因分析

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