muscular的例句大全

Results All patients suffered from fever, headache, sore throat, hoarseness, an muscular ache from head to foot, dry cough with a flu-like illnesss.

结果本组暴发流行的肺炎衣原体肺炎患者均有发热，头痛，全身肌肉酸痛，干咳，声音嘶哑，咽痛等症状。

Spinal brace may have the effect of truck support, still it could increase paraspinal muscular activities of backache patients on various situations.

显示背痛病患者穿著背架可能会造成背肌活动增加。

A case report of spinal muscular atrophy ( adult type) with clinical and pathological examinations

成人型脊髓性肌萎缩&附1例临床及病理报告

Clinical analysis of 129 cases of progressive spinal muscular atrophy

进行性脊肌萎缩症129例临床分析

Prenatal diagnosis of spinal muscular atrophy based on umbilical cord blood

胎儿脐带血产前诊断脊髓性肌萎缩症

Gene diagnosis and prenatal gene diagnosis of spinal muscular atrophy

脊髓性肌萎缩的基因诊断和产前基因诊断研究

Gene Diagnosis of Spinal Muscular Atrophy in Children

儿童脊髓性肌萎缩症的基因诊断

A study on gene diagnosis in childhood-onset spinal muscular atrophy

儿童型脊肌萎缩症基因诊断的研究

Study on the Gene Diagnosis and the Genotype-Phenotype Correlation of Spinal Muscular Atrophy

脊髓性肌萎缩症基因诊断及基因型与表型关系的研究

Objectives To investigate the clinical features and the onset pattern of spinal muscular atrophy.

目的探讨脊肌萎缩症的临床特点和遗传方式。

Evidence of reduced frequency of spinal muscular atrophy type I in the Cuban population

古巴人群Ⅰ型脊肌萎缩发生率降低的依据

The characteristics of spinal muscular atrophy in adults

成人型脊髓性肌萎缩症临床及遗传学研究

Application of quantitative analysis of survival motor neuron copy number in gene diagnosis for type ⅲ spinal muscular atrophy

运动神经元生存基因拷贝数定量分析在Ⅲ型脊髓性肌萎缩症基因诊断中的应用

Methods The clinical data of13 infants suffering from infantile spinal muscular atrophy were analysed.

方法分析13例婴儿型脊髓性肌萎缩症患儿的临床资料。

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

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

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。

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。

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。

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。