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- 定位于12q24的腓骨肌萎缩症2L型10个候选基因的排除克隆Cloning to rule out 10 candidate genes located in chromosome 12q24 for Charcot-Marie-Tooth disease type 2L
- 腓骨肌萎缩症2L型Charcot-Marie-Tooth disease type 2L
- 轴突型腓骨肌萎缩症2L型axonal Charcot-Marie-Tooth disease type 2L
- 本文报告32例腓骨肌萎缩症(PMA)患者的临床及肌电图(EMG)和神经传导速度(NCV)的改变。Clinical, electromyography (EMG) and nerve conduction velocity (NCV) features of 32 cases with peroneal muscular atrophy (PMA) are reported.
- 腓骨肌萎缩症伴神经性耳聋一家系临床和分子遗传学分析Clinical features and molecular genetic analysis of a Charcot-Marie-Tooth disease family with sensorineural deafness
- Wohlfart-Kugelberg-Welandor病，少年近端型脊髓性肌萎缩Wohlfart-Kugelberg-Welandor disease
- 慢性炎性脱髓鞘性周围神经病样表现的腓骨肌萎缩症二例A Charcot-Marie-Tooth disease resembling to chronic inflammatory demyelinating polyradiculoneuropathy: a report of two cases
- 阿伦－杜兴肌萎缩Aran-Duchenne atrophy
- 阿伦-杜兴肌萎缩Aran-Duchenne atrophy
- 眼肌萎缩ocular muscle dystrophy; OMD
- 腓骨肌萎缩Peroneal muscular atrophy
- 痛性肌萎缩algodystrophy; parsonage-Aldren-Turner syndrome
- 夏科肌萎缩Charcot's muscular atrophy
- 跳跃型肌萎缩leaping atrophy
- 夏科氏肌萎缩[医] Charcot's muscular atrophy
- 先天性肌萎缩Amyotrophia congenita; Myophagism congenita
- 糖尿病性肌萎缩diabetic amyotrophia; diabetic amyotrophy
- 霍夫曼氏肌萎缩Hoffmanns muscular atrophy
- 慢性脊髓性肌萎缩chronic spinal muscular atrophy
- 先天性脑性肌萎缩CCMD; congenital cerebromuscular dystrophy
