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- 腓骨肌萎縮癥2F型Charcot-Marie-Tooth disease type 2F
- 定位于12q24的腓骨肌萎縮癥2L型10個(gè)候選基因的排除克隆Cloning to rule out 10 candidate genes located in chromosome 12q24 for Charcot-Marie-Tooth disease type 2L
- 本文報告32例腓骨肌萎縮癥(PMA)患者的臨床及肌電圖(EMG)和神經(jīng)傳導速度(NCV)的改變。Clinical, electromyography (EMG) and nerve conduction velocity (NCV) features of 32 cases with peroneal muscular atrophy (PMA) are reported.
- 腓骨肌萎縮癥伴神經(jīng)性耳聾一家系臨床和分子遺傳學(xué)分析Clinical features and molecular genetic analysis of a Charcot-Marie-Tooth disease family with sensorineural deafness
- 腓骨肌萎縮癥2L型Charcot-Marie-Tooth disease type 2L
- Wohlfart-Kugelberg-Welandor病，少年近端型脊髓性肌萎縮Wohlfart-Kugelberg-Welandor disease
- Werdning-Hoffmann萎縮／?。C合征，家族性脊髓性肌萎縮，嬰兒進(jìn)行性脊髓性肌萎縮Werdning-Hoffmann's atrophy/disease/syndrome
- 腓骨肌型鉛毒性麻痹peroneal type lead palsy
- 慢性炎性脫髓鞘性周?chē)窠?jīng)病樣表現的腓骨肌萎縮癥二例A Charcot-Marie-Tooth disease resembling to chronic inflammatory demyelinating polyradiculoneuropathy: a report of two cases
- 腓肌型肌萎縮peroneal atrophy
- 手肩型肌萎縮leaping atrophy
- 腓骨肌萎縮Peroneal muscular atrophy
- 脊肌萎縮癥spinal muscular atrophy
- 跳躍型肌萎縮leaping atrophy
- 肌萎縮側部硬化癥amyotrophic lateral sclerosis
- 嬰兒型肌萎縮infantile muscular atrophy
- 肌萎縮脊髓側索硬化癥Amyotrophic lateral sclerosis(ALS)
- 腓骨肌萎縮兩家系6例報告Report of 6 Patients with Fibular Amyotrophy in both Family Trees
- 遠端型肌萎縮Distal muscular dystrophy
- 肌萎縮側索硬化癥（ALS）amyotrophic lateral sclerosis (ALS)
