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参考文献

[1] Patzko A, Shy ME. Charcot-Marie-Tooth disease and related genetic neuropathies. Continuum (Minneap-Minn), 2012, 18 (1): 39-59.

[2] Tazir M, Hamadouche T, Nouioua S, et al. Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update. J Neurol Sci, 2014, 347 (1-2): 14-22.

[3] Yiu EM, Brockley CR, Lee KJ, et al. Peripheral nerve ultrasound in pediatric Charcot-Marie-Tooth disease type 1A. Neurology, 2015, 84 (6): 569-574.

[4] Hoyle JC, Isfort MC, Roggenbuck J, et al. The genetics of Charcot-Marie-Tooth disease: current trends and future implications for diagnosis and management. Appl Clin Genet, 2015, 8: 235-243.

[5] Manganelli F, Nolano M, Pisciotta C, et al. Charcot-Marie-Tooth disease: New insights from skin biopsy. Neurology, 2015, 85 (14): 1202-1208.

[6] Corrado B, Ciardi G, Bargigli C. Rehabilitation Management of the Charcot-Marie-Tooth Syndrome: A Systematic Review of the Literature. Medicine (Baltimore), 2016, 95 (17): e3278.

[7] 徐银燕,张江涛,牛婧雯,等.进行性四肢麻木无力4年.中国现代神经疾病杂志,2017,017,17 (1):74-77. xd6ScO3zDIrQ9dcYs7eKAVXBoNmwtJkUFnRYATIwRoTcu8tRT8pThS/+gN2mFl/j

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