muscular atrophy

Objective : To explore the features of electrical physiology and diagnosis stage of infantile spinal muscular atrophy.

目的:分 析婴儿型脊肌萎缩症患儿的临床及电生理表现,探讨本病的临床特点及早期诊断.

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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

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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。

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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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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

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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

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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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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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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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Objective To establish a gene diagnosis assay for spinal muscular atrophy ( SMA ) in children.

目的探讨儿童脊髓性肌萎缩症 ( SMA ) 的特异性基因诊断方法.

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β-thalassemia and Spinal muscular atrophy ( SMA) are two common autosomal recessive diseases.

β地中海贫血和脊髓性肌萎缩是两种常见的单基因遗传病。

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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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Clinical analysis of 129 cases of progressive spinal muscular atrophy

进行性脊肌萎缩症129例临床分析

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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

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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

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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

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Clinical study of 83 cases with spinal muscular atrophy in children

小儿进行性脊髓性肌萎缩83例临床分析

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Used for muscular atrophy, painful rheumatoid arthritis , ridding of damp cold.

用于肌肉萎缩 ﹐ 下肢寒湿痹痛等症.

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Objective : To establish a genetic diagnosis assay for spinal muscular atrophy ( SMA ) in children.

目的: 建立儿童型脊髓性肌萎缩症 ( SMA ) 的特异性基因诊断平台.

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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。

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Juvenile distal muscular atrophy of unilateral upper extremity. Report of 28 muscle biopsies

青年单侧上肢远端肌萎缩症&肌活检及与运动神经元病的鉴别诊断

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With toe ( HSI ) A slow growth, thickening deformation, dry skin thinning, Ganmao exfoliated and muscular atrophy.

伴趾 ( 指 ) 甲生长缓慢, 增厚变形, 皮肤干燥变薄, 汗毛脱落和肌肉萎缩.

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In the 58 cases, only 20 ( 34.48%) patients had good function recovery; 26 ( 44.83%) suffered from so-called paraplegia sydrome including anchylosis, muscular atrophy, bed sore, secondary infection, osteoporosis, and the symptoms showed a tendency to aggravate.

58例中，功能恢复较好者20例（34.48%），26例（44.83%）患者发生关节僵硬、肌肉萎缩、压疮、继发感染、骨质疏松等截瘫综合征，且症状呈加剧趋势。

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The effect of passive movement on denervated muscular atrophy in mice

被动活动对小鼠失神经支配肌肉萎缩的影响

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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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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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Gene Diagnosis of Spinal Muscular Atrophy in Children

儿童脊髓性肌萎缩症的基因诊断

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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

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Experimental Study of the Effects of Composite Pseudostellaria Granule on Denervated Muscular Atrophy

复方太子参颗粒延缓失神经支配骨骼肌萎缩的实验研究

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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

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