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- 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
- 腓骨肌萎縮癥2L型Charcot-Marie-Tooth disease type 2L
- 軸突型腓骨肌萎縮癥2L型axonal 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
- Wohlfart-Kugelberg-Welandor病，少年近端型脊髓性肌萎縮Wohlfart-Kugelberg-Welandor disease
- 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
- 阿倫－杜興肌萎縮Aran-Duchenne atrophy
- 阿倫-杜興肌萎縮Aran-Duchenne atrophy
- 眼肌萎縮ocular muscle dystrophy; OMD
- 腓骨肌萎縮Peroneal muscular atrophy
- 痛性肌萎縮algodystrophy; parsonage-Aldren-Turner syndrome
- 夏科肌萎縮Charcot's muscular atrophy
- 跳躍型肌萎縮leaping atrophy
- 夏科氏肌萎縮[醫] Charcot's muscular atrophy
- 先天性肌萎縮Amyotrophia congenita; Myophagism congenita
- 糖尿病性肌萎縮diabetic amyotrophia; diabetic amyotrophy
- 霍夫曼氏肌萎縮Hoffmanns muscular atrophy
- 慢性脊髓性肌萎縮chronic spinal muscular atrophy
- 先天性腦性肌萎縮CCMD; congenital cerebromuscular dystrophy
