- Cornblath, D.V. Evaluation of the Patient with Peripheral Neuropathy: The Challenges. Diagnosis and Management of Peripheral Nerve Disorders. Eds. Mendell, J., et al. New York: Oxford University Press. 2001. 3-29.
- Barohn, R. Approach to Peripheral Neuropathy and Neuronopathy. Seminars in Neurology 18. 1998. 7-18.
- Bird, T. Charcot-Marie-Tooth Hereditary Neuropathy Overview. GeneReviews, GeneClinics. 2001. http://www.geneclinics.org
- Boerkoel, C.F., et al. Periaxin mutations cause recessive Dejerine-Sottas neuropathy. American Journal of Human Genetics. 2001; 68:325-333.
- Guilbot, A., et al. A mutation in Periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease. Human Molecular Genetics. 2001; 10:415-421.
- Takashima H., et al. Periaxin Mutations Cause a Broad Spectrum of Demyelinating Neuropathies. Annals of Neurology. 2002; 51:709-715.
- Lovelace, R.E., et al. Hereditary Neuropathies. Meritt's Textbook of Neurology, Ninth Edition. Ed. Rowland, L.P. Baltimore, MD: Williams & Wilkins. 1995. 651-657.
- Mendell, J.R., et al. Hereditary Motor and Sensory Neuropathies and Giant Axonal Neuropathy. Diagnosis and Management of Peripheral Nerve Disorders. Ed. Mendel, J.R. New York, NY: Oxford University Press. 2001. 429-459.
- Boerkoel, C.F., and Lupski, J.R. Hereditary Motor and Sensory Neuropathies. Principles and Practice of Medical Genetics, Fourth Edition. Eds. Rimoin, D.L., et al. London: Harcourt. 2002. 3303-3320.
- Jaradeh, S. Hereditary Neuropathies. Proceedings from the American Academy of Neurology 54th Annual Meeting. 2002.
- Garcia, C.A. The Clinical Features of Charcot-Marie-Tooth Disorders. Charcot-Marie-Tooth Disorders: A Handbook for Primary Care Physicians. Ed. G.J. Parry. Upland, PA: Charcot-Marie-Tooth Association. 1995. 5-17.
- Bird, T. Charcot-Marie-Tooth Neuropathy Type 4. GeneReviews, GeneClinics. 2001. http://www.geneclinics.org
- Bird, T. Charcot-Marie-Tooth Neuropathy Type X. GeneReviews, GeneClinics. 2001. http://www.geneclinics.org
- Lupski, J.R. and Garcia, C.A. Charcot-Marie-Tooth Peripheral Neuropathies and Related Disorders. The Metabolic and Molecular Bases of Inherited Diseases, Eighth Edition. Eds. Scriver, C.R., et al. New York: McGraw-Hill. 2001. 5759-5788.
- Bird, T. Charcot-Marie-Tooth Neuropathy Type 1. GeneReviews, GeneClinics. 2001. http://www.geneclinics.org
- Carter G.T., et al. Neuropathic pain in Charcot-Marie-Tooth disease. Archives of Physical Medicine and Rehabilitation. 1998; 79:1560-1564.
- Graf W.D, et al. Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1A. Cancer 1999; 77:1356-1362.
- Chance, P.F. Overview of Hereditary Neuropathy with Liability to Pressure Palsies. Annals of the New York Academy of Sciences 1999;883:14-21.
- Tyson, J. et al., Deletions of Chromosome 17p11.2 in multifocal neuropaties. Annals of Neurology 1996;39(2):180-6.
