References
- Basu A, Al-Shenar S, Ray S. 2006. Pregnancy in Charcot–Marie–Tooth disease. Journal of Obstetrics and Gynaecology: The Journal of the Institute of Obstetrics and Gynaecology 26:370.
- Bird TD. 1998. Charcot–Marie–Tooth (CMT) hereditary neuropathy overview [updated 2018]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews®. Seattle (WA): University of Washington, Seattle. p. 1993–2018. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1358/
- Brock M, Guinn C, Jones M. 2009. Anesthetic management of an obstetric patient with Charcot–Marie–Tooth disease: a case study. AANA Journal 77:335–337.
- Herman M, Delmis J, Ivanisević M, Zupić T. 2010. Pregnancies and deliveries in patients with Charcot–Marie–Tooth disease. Acta Medica Croatica: Casopis Hravatske Akademije Medicinskih Znanosti 64:215–220.
- Hoff J, Gilhus N, Daltveit A. 2005. Pregnancies and deliveries in patients with Charcot–Marie–Tooth disease. Neurology 64:459–462.
- Johnson N, McCorquodale D, Pucillo E. 2016. Management of Charcot Marie Tooth disease: improving long-term care with a multidisciplinary approach. Journal of Multidisciplinary Healthcare 9:7–19.
- Pereira A, Dias L, Ribeiro E. 2014. Delivery in Charcot–Marie–Tooth (CMT) disease: neurological exacerbation after epidural anesthesia. European Journal of Anaesthesiology 31:178–179.
- Rudnik-Schoneborn S, Rohrig D, Nicholson G, Zerres K. 1993. Pregnancy and delivery in Charcot–Marie–Tooth disease type 1. Neurology 43:2011–2016.