• "Ultrasound of radial, ulnar, median, and sciatic nerves in healthy subjects and patients with hereditary motor and sensory neuropathies", Heinemeyer O.et al; Ultrasound Med. Biol. 1999 25/3 (481-485)
• "Erythrocyte alkaline phosphatase in patients with myotonic muscle disorders." Goldemberg AL;et.al., : Invest Clin 1996 Dec; 37 (4): 247-53
• "Diagnosis of monogenic diseases of the peripheral nervous system": Haupt A; Epplen JT; Dtsch Med Wochenschr 1996 Nov 22; 121 (47): 1469-72
• "MRI of skeletal muscles in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths. EXPERIMENTAL TREATMENTS FOR CMT"; Bono F, et al; Eur Neurol. 1998;39(3):191-2. 

EMG Findings in CMT
 

• "Demyelinating X-linked charcot-marie-tooth disease: unusual electrophysiological findings." Tabaraud F, et al. Muscle Nerve. 1999 Oct;22(10):1442-7.
• "Peripheral late waves in patients with hereditary motor sensory neuropathy. "Christova LG, et al. Electromyogr Clin Neurophysiol. 1999 Sep;39(6):345-8.
• "[Comparison of electrophysiological findings between CIDP and HMSN-1]. " Hasegawa O, et al. No To Shinkei. 1999 May;51(5):411-4. Japanese.
• "Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion", Mouton P, et al; Neurology. 1999 Apr 22;52(7):1440-6
• "Clinical and electrophysiological findings and follow-up in tarsal tunnel syndrome" Mondelli M, et al; Electroencephalogr Clin Neurophysiol. 1998 Oct;109(5):418-25. 
• "Correlation between denervation activity and compound muscle action potential amplitude in hereditary motor and sensory neuropathy I and II."; Paraskevas GP, et al.; Electromyogr Clin Neurophysiol. 1998 Sep;38(6):343-7
• "Surface EMG and myosonography in the detection of fasciculations: a comparative study.", Wenzel S, et al; J Neuroimaging. 1998 Jul;8(3):148-54.
• "Electrophysiological findings in hereditary motor and sensory neuropathy type I and II--a conduction velocity study." Emeryk-Szajewska B., et al; Electromyogr Clin Neurophysiol. 1998 Mar;38(2):95-101. 
• "Correlation between varying levels of PMP22 expression and the degree of demyelination and reduction in nerve conduction velocity in transgenic mice",Huxley C, et al;Hum Mol Genet 1998 Mar;7(3):449-458
• "Hereditary sensorimotor neuropathy in electrophysiological studies", Emeryk-Szajewska B, et al.; Neurol Neurochir Pol. 1998 Mar-Apr;32(2):295-308.
• "Electrodiagnosis in neuromuscular disease." ; Krivickas LS; Phys Med Rehabil Clin N Am. 1998 Feb;9(1):83-114, vi. Review.
• "Charcot-Marie-Tooth disease: electromyography is still useful in diagnosis and classification": Birouk N., et al; Rev Neurol (Paris). 1997 Dec;153(12):727-36. 
• "Electrophysiological studies in the different genotypes of Charcot-Marie-Tooth disease" England J.D.; Garcia C.A. CURR. OPIN. NEUROL. 1996 9/5 (338-342)

Experimental Treatments for CMT
 

• "Charcot-Marie-Tooth disease type 1 and 2-an immunohistochemical study of muscle fibre cytoskeletal proteins and a marker for muscle fibre regeneration", Ericson U, et al; Eur J Neurol. 1998 Nov;5(6):545-551
• "Growth hormone replacement in an adult with mild growth hormone deficiency and hereditary motor and sensory neuropathy: growth hormone restores independent mobility" Lissett CA, et al; Horm Res. 1998;50(4):232-6. 
• "Induction of experimental autoimmune neuritis with peripheral myelin protein-22". Gabriel CM, et al; Brain. 1998 Oct;121 ( Pt 10):1895-902.

Eyesight and CMT

• "Hereditary motor and sensory neuropathy with congenital glaucoma. Report on a family. " Arruda WO, et al. Arq Neuropsiquiatr. 1999 Jun;57(2A):190-4.
• "Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy" Chalmers R.M.;et.al, J. Neurol. Neurosurg. Psychiatry 1997 62/4 (385-387)
• "Retinal changes in familial peripheral sensory and motor neuropathy associated with anterior cervical hypertrichosis." Garty BZ, et al; Pediatr Ophthalmol Strabismus. 1997 Sep-Oct;34(5):309-12. 
• "Hereditary motor and sensory neuropathy with spastic paraplegia and optic atrophy: report on a family." Dillmann U, et al; J Neurol. 1997 Sep;244(9) :562-5.