Stavale J N, Cavaliere M J, Gagioti S M, Atalla A, Guidugli Neto J
Arq Neuropsiquiatr. 1984 Jun;42(2):146-51. doi: 10.1590/s0004-282x1984000200007.
Myasthenia gravis is a neuromuscular disease characterized by excessive fatigability of muscle function and particularly involves muscles innervated by the cranial nerves. It is believed that the defect is in the neuromuscular junction. The authors studied histochemical and morphometric findings in 4 patients with myasthenia gravis showing that the type II fibres were significantly smaller than the type I fibres.
重症肌无力是一种神经肌肉疾病，其特征是肌肉功能过度易疲劳，尤其累及由颅神经支配的肌肉。据信缺陷在于神经肌肉接头。作者研究了4例重症肌无力患者的组织化学和形态测量结果，发现II型纤维明显小于I型纤维。
