REFERENCES
- Bähr, M., Andres, F., Timmerman, V., Nelis, E., Broeckhoven, V. C., & Dichgans, J. (1999). Central visual, acoustic, and motor pathway involvement in a Charcot–Marie–Tooth family with an Asn205Ser mutation in the connexin32 gene. Journal of Neurology, Neurosurgery, and Psychiatry, 66, 202–206.
- Fischbeck, K. H., Abel, A., Lin, G. S., & Scherer, S. S. (1999). X-linked Charcot–Marie–Tooth Disease and Connexin32. Annals of the New York Academy of Sciences, 883, 36–41.
- Kawakami, H., Inoue, K., Sakakihara, I., & Nakamura, S. (2002). Novel mutation in X-linked Charcot–Marie–Tooth disease associated with CNS impairment. Neurology, 59, 923–926.
- Panas, M., Kalfakis, N., Karadimas, C., & Vassilopoulos, D. (2001). Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 gene. Neurology, 57, 1906–1908.
- Panas, M., Karadimas, C., Avramopoulos, D., & Vassilopoulos, D. (1998). Central nervous system involvement in four patients with Charcot–Marie–Tooth disease with connexin 32 extracellular mutations. Journal of Neurology, Neurosurgery, and Psychiatry, 65, 947–948.
- Paulson, H. L., Garbern, J. Y., Hoban, T. F., Krajewski, K. M., Lewis, R. A., Fischbeck, K. H., (2002). Transient CNS white matter abnormality in X-linked Charcot–Marie–Tooth disease. Annals of Neurology, 52, 429–434.
- Schelhaas, H. J., Van Engelen, B. G., Gabreëls-Festen, A. A., Hageman, G., Vliegen, J. H., Van Der Knaap, M. S., (2002). Transient cerebral white matter lesions in a patient with connexin 32 missense mutation. Neurology, 59, 2007–2008 .
- Sevilla, T., Cuesta, A., Chumillas, M. J., Mayordomo, F., Pedrola, L., Palau, F., (2003). Clinical, electrophysiological, and morphological findings of Charcot–Marie–Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene. Brain, 126, 2023–2033.
- Sevilla, T., Jaijo, T., Nauffal, D., Collado, D., Chumillas, M. J., Vilchez, J. J., (2008). Vocal cord paresis and diaphragmatic dysfunction are severe and frequent symptoms of GDAP1-associated neuropathy. Brain, 131, 3051–3061.
- Taylor, R. A., Simon, E. M., Marks, H. G., & Scherer, S. S. (2003). The CNS phenotype of X-linked Charcot–Marie–Tooth disease, more than a peripheral problem. Neurology, 61, 1475–1478.