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- 腓骨肌萎缩症2F型Charcot-Marie-Tooth disease type 2F
- 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
- 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
- 腓骨肌萎缩症2L型Charcot-Marie-Tooth disease type 2L
- Wohlfart-Kugelberg-Welandor病，少年近端型脊髓性肌萎缩Wohlfart-Kugelberg-Welandor disease
- Werdning-Hoffmann萎缩／病／综合征，家族性脊髓性肌萎缩，婴儿进行性脊髓性肌萎缩Werdning-Hoffmann's atrophy/disease/syndrome
- 腓骨肌型铅毒性麻痹peroneal type lead palsy
- 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
- 腓肌型肌萎缩peroneal atrophy
- 手肩型肌萎缩leaping atrophy
- 腓骨肌萎缩Peroneal muscular atrophy
- 脊肌萎缩症spinal muscular atrophy
- 跳跃型肌萎缩leaping atrophy
- 肌萎缩侧部硬化症amyotrophic lateral sclerosis
- 婴儿型肌萎缩infantile muscular atrophy
- 肌萎缩脊髓侧索硬化症Amyotrophic lateral sclerosis(ALS)
- 腓骨肌萎缩两家系6例报告Report of 6 Patients with Fibular Amyotrophy in both Family Trees
- 远端型肌萎缩Distal muscular dystrophy
- 肌萎缩侧索硬化症（ALS）amyotrophic lateral sclerosis (ALS)
