18-19-4　ⓔ文献

  1. Thomas PK, Dyck PJ eds: Peripheral Neuropathy, 4th ed, WB Saunders, 2005.

  2. 橋口昭大，髙嶋　博：遺伝性ニューロパチー．日本内科学会雑誌，2019; 108: 1545–1551.

  3. Yoshimura A, Yuan JH, et al: Genetic profile and onset features of 1005 patients with Charcot–Marie–Tooth disease in Japan. J Neurol Neurosurg Psychiatry, 2018; 90: 195–202.

  4. 中川正法，滋賀健介：Charcot–Marie–Tooth病の治療の現状と展望．神経内科，2009; 70: 366–372.

  5. 髙嶋　博：基礎医学的に見た Charcot–Marie–Tooth病の病態と治療．難病と在宅ケア，2008; 14: 40–44.

  6. Hattori N, Yamamoto M, et al: Study Group for Hereditary Neuropathy in Japan. Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin–related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients. Brain, 2003; 126: 134–151.

  7. Koike H, Hirayama M, et al: Age associated axonal features in HNPP with 17p11.2 deletion in Japan. J Neurol Neurosurg Psychiatry, 2005; 76: 1109–1114.

  8. 清水　潤：Hereditary sensory and autonomic neuropathy. Peripheral Nerve, 2013; 24: 23–30.

  9. 秋口一郎監：カラーアトラス末梢神経の病理，中外医学社，2010．

  10. Neuromuscular Disease Center. http://neuromuscular.wustl.edu/