Methods The spinal nerve roots were injured in 20 rabbits.

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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Electromyogram ( emg) and muscle biopsy in patients with chronic spinal muscular atrophy

慢性脊髓性肌萎缩的肌电图及肌活检

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Detection of survival motor neuron gene deletions using allele-specific amplification in patients with spinal muscular atrophy

等位基因特异性扩增法检测脊髓性肌萎缩运动神经元生存基因缺失

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The diagnosis value of SMN gene deletions in progressive spinal muscular atrophy

运动神经元存活基因对进行性脊肌萎缩症的诊断价值

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