Nerve Anatomy& Physiology in CMT

• "Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22." Fabrizi GM, et al. Neurology. 1999 Sep 11;53(4):846-51.
• "Myelin deficiencies in both the central and the peripheral nervous systems associated with a SOX10 mutation. " Inoue K, et al Ann Neurol. 1999 Sep;46(3):313-8.
• "Ultrastructural changes in peripheral nerve in hereditary motor and sensory neuropathy-Lom. " King RH, et al. Neuropathol Appl Neurobiol. 1999 Aug;25(4):306-12.
• "Axonal pathology in demyelinating diseases" Scherer S; Ann Neurol 1999 Jan; 45 (1): 6-7
• "Sympathetic skin response differentiates hereditary sensory autonomic neuropathies III and IV",Hilz MJ, et al;Neurology. 1999 May 12;52(8):1652-7. 
• "Analysis of sensory function in Charcot-Marie-Tooth disease.", Ericson U, et al; Acta Neurol Scand. 1999 May;99(5):291-6.
• "Charcot-Marie-Tooth disease: histopathological features of the peripheral myelin protein (PMP22) duplication (CMT1A) and connexin32 mutations (CMTX1).,Sander S, Nicholson GA, et al;Muscle Nerve 1998 Feb;21(2):217-225 
• "Preliminary study of large and small peripheral nerve fibers inCharcot Marie Tooth disease, type I.",Hanson P, Deltombe T;Am J Phys Med Rehabil 1998 Jan;77(1):45-48
• "Altered neurofilament phosphorylation and beta tubulin isotypes in Charcot-Marie-Tooth disease type 1.",Watson, D.F., et al;Neurology 44:2383-2387:1994.

Other Diseases and CMT

• "Vincristine treatment revealing asymptomatic hereditary motor sensory neuropathy type 1A. " Mercuri E, et al. Arch Dis Child. 1999 Nov;81(5):442-3.
• "Autonomic function in patients with hereditary motor and sensory neuropathy type I and Lambert-Eaton myasthenic syndrome. " Kalmijn S, et al. Electromyogr Clin Neurophysiol. 1999 Sep;39(6):349-53.
• "Cognitive, psychosocial, and educational issues in neuromuscular disease." Sigford BJ; Lanham RA Jr;: Phys Med Rehabil Clin N Am 1998 Feb; 9 (1): 249-70
• "Charcot MarieTooth disease type 2 with restless legs syndrome", Gemignani F, et al; Neurology. 1999 Mar 23;52(5):1064-6
• "Triple association of Crohn disease, multiple sclerosis, Charcot Marie Tooth disease. Case report", Gil H, et al; Rev Med Interne. 1999 Mar;20(3):288-9
• "Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies.", Naef R, et al; Neurobiol Dis. 1999 Feb;6(1):1-14

Pain in CMT
 

• "Neuropathic Pain in Charcot-Marie-Tooth Disease" G.T. Carter, et al; Archives of Physical Medicine and Rehabilitation, Dec. 1998, V.79 pp1560-1564
• "Neuropathic spinal arthropathy in Charcot-Marie-Tooth disease. A case report. "Anand N, et al; J Bone Joint Surg Am. 1997 Aug;79(8):1235-9

Pregnancy and CMT

• "Pregnancy after preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1A.", Mol Hum Reprod 1998 Oct; 4 (10): 978-84 
• "Charcot-Marie-Tooth disease and pregnancy: report of a case." Bellina JH, et al. ; J La State Med Soc. 1973 Nov;125(11):393-5.
• "Effect of pregnancy on the course of Charcot-Marie-Tooth neural amyotrophy". Badalian LO, et al; Akush Ginekol (Mosk). 1986 Jun;(6):70-1.
• "Pregnancy complicated by Charcot-Marie-Tooth disease, requiring intermittent ventilation. "Byrne DL, et al.; Br J Obstet Gynaecol. 1992 Jan;99(1):79-80.

Prenatal Diagnosis of CMT

• "Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by interphase fluorescence in situ hybridization.",Kashork CD, et al.;Prenat Diagn. 1999 May;19(5):446-9
• "Prenatal diagnosis of Charcot-Marie-Tooth disease" Lebo RV; Prenat Diagn 1998 Feb;18(2):169-172

Rehabilitation in CMT

• "Daytime somnolence in myotonic dystrophy. "Phillips MF, et al. J Neurol. 1999 Apr;246(4):275-82.
• "Improvement of muscle function in Charcot-Marie-Tooth disease by transcutaneous electric nerve stimulation"; Hassel B; Muscle Nerve 1998 Feb;21(2):267-268
• "Quadriceps strength and timed motor performances in myotonic dystrophy, Charcot-Marie-Tooth disease, and healthy subjects": .Lindeman E,et al; Clin Rehabil. 1998 Apr;12(2):127-35. 
• "Type I Charcot-Marie-Tooth syndrome. Disability and management".; Wicklein EM, et al.; Nervenarzt. 1997 Apr;68(4):358-62.