Respiratory Problems in CMT

• "Respiratory insufficiency in Charcot-Marie-Tooth disease. ";Hirsch NP; Anaesthesia. 1998 Oct;53(10):1034.
• "Diaphragmatic weakness in hereditary motor and sensory neuropathy"; Green MM, et al; J Neurol Neurosurg Psychiatry. 1991 Aug;54(8):759. 
• "Phrenic Nerve Involvement in Charcot-Marie-Tooth Disease. A Pathologic Documentation" D. Gilchrist, et al; Chest; 1989 ; 96; pp1197-1199
• "Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type 1 ; P.Eichacker, A. et al,; Arch. Internal Medicine 1988; 18;pp1739-1740 
• "Charcot-Marie-Tooth disease and respiratory failure."; Dyer EL, et al.; Chest. 1988 Jan;93(1):221.
• "Respiratory Muscle Weakness in Charcot Marie Tooth Disease" ,C.M.Laroche, et al; Thorax 1988; 43; pp468-479

Surgery for CMT
 

• "Triple arthrodesis: twenty-five and forty-four-year average follow-up of the same patients."Saltzman CL, et al. J Bone Joint Surg Am. 1999 Oct;81(10):1391-402.
• "Restoring hand function in patients with severe polyneuropathy: the role of electromyography before tendon transfer surgery." Mackin GA, et al. J Hand Surg [Am]. 1999 Jul;24(4):732-42
• "The Charcot joint " {when associated with Charcot Marie Tooth Disease} Zwipp H, et al. Orthopade. 1999 Jun;28(6):550-8. German
• "The periacetabular osteotomy. Minimum 2 year followup in more than 100 hips. "Trumble SJ, et al. Clin Orthop. 1999 Jun;(363):54-63.
• "Orthopedic management of neuromuscular disorders in children." Birch, JG; Semin Pediatr Neurol. 1998 Jun;5(2):78-91.
• "Surgical arthrodesis of the neuropathic foot. A salvage procedure",Bono JV. Roger DJ. Jacobs RL;Clinical Orthopaedics & Related Research. (296):14-20, 1993 Nov
• "Long-term results of triple arthrodesis in Charcot-Marie-Tooth disease.",Wetmore-RS; Drennan-JC; J-Bone-Joint-Surg-Am. 1989 Mar; 71(3): 417-22
• "Plantar release in the correction of deformities of the foot in childhood",Sherman-FC; Westin-GW;J-Bone-Joint-Surg-Am. 1981 Dec; 63(9): 1382-9 

Type I CMT (Demyelinating)
 

• "Atypical phenotype of charcot-marie-tooth disease type 1A."Murakami T, et al. Muscle Nerve. 1999 Nov;22(11):1593-6.
• "[A sporadic case of Charcot-Marie-Tooth disease type 1 A associated with a duplication in chromosome 17 p11.2-p12]." Inoue M, et al. No To Hattatsu. 1999 Sep;31(5):452-7. Japanese.
• "Clinical and electrophysiological study in French-Canadian population with Charcot-Marie-tooth disease type 1A associated with 17p11.2 duplication."Dupre N, et al. Can J Neurol Sci. 1999 Aug;26(3):196-200.
• "[A family of hereditary motor and sensory neuropathy type 1B showing a marked difference of neurological disability score among affected family members]. "Ohnishi A, et al. Sangyo Ika Daigaku Zasshi. 1999 Jun 1;21(2):149-56. Japanese.
• "Charcot MarieTooth disease type I diagnosed in a 5-year-old boy after vincristine neurotoxicity, resulting in maternal diagnosis", Olek MJ, et al; J Am Osteopath Assoc. 1999 Mar;99(3):165-7.
• "Charcot-Marie-Tooth disease type 1A presenting as calf hypertrophy and muscle cramps".Krampitz DE.,et al; Neurology. 1998 Nov;51(5):1508-9. 
• "Pathogenesis of Charcot-Marie-Tooth 1A (CMT1A) neuropathy.", Hanemann CO, et al; Trends Neurosci. 1998 Jul;21(7):282-6. Review.
• "Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood: a longitudinal clinical and electrophysiologic study." .; Garcia A., et.al; Neurology. 1998 Apr;50(4):1061-7

Type II CMT (Axonal)
 

• "A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3. " Bouhouche A, et al. Am J Hum Genet. 1999 Sep;65(3):722-7.
• "[A case of hereditary sensory autonomic neuropathy type II with late onset]. " Shimoya K, et al. Rinsho Shinkeigaku. 1999 May;39(5):551-4. Japanese.
• "Charcot MarieTooth disease type 2 and P0 gene mutations", Pareyson D, et al; Neurology. 1999 Mar 23;52(5):1110-1"
• "Autosomal recessive type II hereditary motor and sensory neuropathy with acrodystrophy", Thomas, P.K.;J Neurol. 1999 Feb;246(2):107-12
• "Familial spastic paraplegia, axonal sensory-motor polyneuropathy and bulbar amyotrophy with facial dysmorphia: New cases of Troyer-like syndrome", Bertini E.et al; Eur. J. Paediatric Neurol. 1998 2/5 (245-254)

Vocal Cord Problems and CMT
 

• "Varying occurrence of vocal cord paralysis in a family with autosomal dominant hereditary motor and sensory neuropathy. "Donaghy M, et al J Neurol. 1999 Jul;246(7):552-5.
• "Laryngeal electromyographic findings in Charcot-Marie-Tooth disease type II."Dray TG, et al. Arch Neurol. 1999 Jul;56(7):863-5.
• "Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis.", Dyck,P.J.et al; Ann Neurol 35:608-615:1994