Charcot–Marie–Tooth Disease

Encyclopedia of the Neurological Sciences: Volumes 1-4

Volumn 1, Issue , 2003, Pages V1-676-V1-686

  Li, Jun ^a   Lewis, Richard A ^a   Shy, Michael E ^b  

^a WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 18744372028     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B0-12-226870-9/00882-0     Document Type: Chapter

References (12)

1. P.F. Chance (1999) Overview of hereditary neuropathy with liability to pressure palsies. Ann. N. Y. Acad. Sci. 883 14-21.
2. P.J. Dyck and E.H. Lambert (1968) Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations. Arch. Neurol. 18 619-625.
3. A.F. Hahn, P.J. Ainsworth, C.C. Naus, et al. (2000) Clinical and pathological observations in men lacking the gap junction protein connexin 32. Muscle Nerve 23 S39-S48.
4. A. Harding (1993) Inherited neuronal atrophy and degeneration predominantly of lower motor neurons. P.J. Dyck, J. Griffin, P. Low, J. Poduslo (Eds) Peripheral Neuropathy Philadelphia: Saunders 1051-1064.
5. J. Kamholz, D. Menichella, A. Jani, et al. (2000) Charcot–Marie–Tooth disease type 1: Molecular pathogenesis to gene therapy. Brain 123 222-233.
6. K.M. Krajewski, R.A. Lewis, D.R. Fuerst, et al. (2000) Neurological dysfunction and axonal degeneration in Charcot–Marie–Tooth disease type 1A. Brain 123 1516-1527.
7. R.A. Lewis, A.J. Sumner and M.E. Shy (2000) Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis. Muscle Nerve 23 1472-1487.
8. G. Nicholson and J. Nash (1993) Intermediate nerve conduction velocities define X-linked Charcot–Marie–Tooth neuropathy families. Neurology 43 2558-2564.
9. P.K. Thomas, W. Marques, M.B. Davis, et al. (1997) The phenotypic manifestations of chromosome 17p11.2 duplication. Brain 120 465-478.
10. J.M. Vance (2000) The many faces of Charcot–Marie–Tooth disease. Arch. Neurol. 57 638-640.
11. L.E. Warner, M.J. Hilz, S.H. Appel, et al. (1996) Clinical phenotypes of different MPZ (P0) mutations may include Charcot–Marie–Tooth type 1B, Dejerine–Sottas, and congenital hypomyelination. Neuron 17 451-460.
12. C. Zhao, J. Takita, Y. Tanaka, et al. (2001) Charcot–Marie–Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta. Cell 105 587-597.