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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
