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Charcot-marie-Tooth disease : a case presenting with hyperreflexiaCHI-CHANG SHIEH; PEN-JUNG WANG; HUEY-JUAN LIN et al.Xiaoér keyi xuéhuì zázhì. 1990, Vol 31, Num 2, pp 116-121, issn 0001-6578, 6 p.Article

MR imaging in hypertrophic neuropathy : a case of hereditary motor and sensory neuropathy, type 1 (Charcot-Marie-Tooth)CHOI, S. K; BOWERS, R. P; BUCKTHAL, P. E et al.Clinical imaging. 1990, Vol 14, Num 3, pp 204-207, issn 0899-7071Article

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Schwerhörigkeit als Symptom der neutralen Muskelatrophie (Charcot-Marie-Tooth-Krankheit) = La surdité, symptome de maladie de Charcot marie Tooth = Deafness as a symtom of Charcot Marie Tooth diseaseLAUBERT, A.HNO. Hals-, Nasen-, Ohrenärzte. 1986, Vol 34, Num 10, pp 434-437, issn 0017-6192Article

Anesthetic management for cesarean section of a patient with Charcot-Marie-Thooth diseaseBRIAN, J. E. JR; BOYLES, G. D; QUIRK, J. G. JR et al.Anesthesiology (Philadelphia). 1987, Vol 66, Num 3, pp 410-412, issn 0003-3022Article

Myasthenia gravis complicating Charcot-Marie-Tooth disease: report of a caseBERGER, J. R; RAM AYYAR, D; KIMURA, I et al.Journal of clinical neuro-ophthalmology. 1985, Vol 5, Num 2, pp 76-80, issn 0272-846XArticle

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Charcot-Marie-Tooth disease: Genetic and clinical spectrum in a Spanish clinical seriesSIVERA, Rafael; SEVILLA, Teresa; ESPINÓS, Carmen et al.Neurology. 2013, Vol 81, Num 18, pp 1617-1625, issn 0028-3878, 9 p.Article

Clinical and electrophysiological features in charcot-marie-tooth disease with mutations in the NEFL geneMILTENBERGER-MILTENYI, Gabriel; JANECKE, Andreas R; WANSCHITZ, Julia V et al.Archives of neurology (Chicago). 2007, Vol 64, Num 7, pp 966-970, issn 0003-9942, 5 p.Article

A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2)CONFORTI, F. L; MUGLIA, M; PELUSO, G et al.Neurology. 2004, Vol 63, Num 7, pp 1327-1328, issn 0028-3878, 2 p.Article

Anaesthesia for Charcot-Marie-Tooth disease : a review of 86 casesANTOGNINI, J. F.Canadian journal of anaesthesia. 1992, Vol 39, Num 4, pp 398-400, issn 0832-610XArticle

Anesthetic management for the child with Charcot-Marie-tooth diseaseGREENBERG, R. S; PARKER, S. D.Anesthesia and analgesia. 1992, Vol 74, Num 2, pp 305-307, issn 0003-2999Article

Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees : additional evidence for a third autosomal CMT1 locusCHANCE, P. F; MATSUNAMI, N; LENSCH, W et al.Neurology. 1992, Vol 42, Num 10, pp 2037-2041, issn 0028-3878Article

Briefly noted : failure of somatosensory-evoked-potential monitoring in sensorimotor neuropathyKRISHNA, M; TAYLOR, J. F; BROWN, M. C et al.Spine (Philadelphia, PA. 1976). 1991, Vol 16, Num 4, issn 0362-2436, p. 479Article

Diaphragmatic weakness in hereditary motor and sensory neuropathyHARDIE, R; HARDING, A. E; HIRSCH, N et al.Journal of neurology, neurosurgery and psychiatry. 1990, Vol 53, Num 4, pp 348-350, issn 0022-3050Article

Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17DEFESCHE, J. C; HOOGENDIJK, J. E; DE VISSER, M et al.Neurology. 1990, Vol 40, Num 9, pp 1450-1453, issn 0028-3878, 4 p.Article

Visual and somatosensory evoked potentials in hereditary motor-sensory neuropathiesNEVSIMALOVA, S; PONCA, I; FIKSA, J et al.Schweizer Archiv für Neurologie und Psychiatrie (1985). 1990, Vol 141, Num 3, pp 217-228, issn 0258-7661, 12 p.Article

Gilles de la Tourette-Syndrom und spinale Muskelatrophie vom Peronealtyp Eine Kasuistik = Syndrome de Gilles de la Tourette et amyotrophie médullaire péronière = Gilles de la Tourette syndrome and peroneal spinal amyotrophy. Case reportSCHOLDERLE, M; GREIL, W; PONGRATZ, D et al.Nervenarzt. 1987, Vol 58, Num 8, pp 514-518, issn 0028-2804Article

Vestibular impairment in patients with Charcot-Marie-Tooth diseasePORETTI, Andrea; PALLA, Antonella; TARNUTZER, Alexander A et al.Neurology. 2013, Vol 80, Num 23, pp 2099-2105, issn 0028-3878, 7 p.Article