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

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

Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4HFABRIZI, G. M; TAIOLI, F; CAVALLARO, T et al.Neurology. 2009, Vol 72, Num 13, pp 1160-1164, issn 0028-3878, 5 p.Article

A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG functionTSAI, Pei-Chien; HUANG, Yen-Hua; YET, Shaw-Fang et al.Neurology. 2014, Vol 83, Num 10, pp 903-912, issn 0028-3878, 10 p.Article

Charcot—Marie—Tooth disease: frequency of genetic subtypes and guidelines for genetic testingMURPHY, Sinead M; LAURA, Matilde; LUNG, Michael P. T et al.Journal of neurology, neurosurgery and psychiatry. 2012, Vol 83, Num 7, pp 706-710, issn 0022-3050, 5 p.Article

ADULT ONSET CHARCOT―MARIE―TOOTH DISEASE TYPE 1D WITH AN Arg381Cys MUTATION OF EGR2BRIANI, Chiara; TAIOLI, Federica; LUCCHETTA, Marta et al.Muscle & nerve. 2010, Vol 41, Num 6, pp 888-889, issn 0148-639X, 2 p.Article

Neuropathy progression in Charcot-Marie-Tooth disease type 1ASHY, M. E; CHEN, L; SWAN, E. R et al.Neurology. 2008, Vol 70, Num 5, pp 378-383, issn 0028-3878, 6 p.Article

SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3NAKHRO, Khriezhanuo; PARK, Jin-Mo; JI YON KIM et al.Neurology. 2013, Vol 81, Num 2, pp 165-173, issn 0028-3878, 9 p.Article

SURF1 deficiency causes demyelinating Charcot-Marie-Tooth diseaseECHANIZ-LAGUNA, Andoni; GHEZZI, Daniele; ZEVIANI, Massimo et al.Neurology. 2013, Vol 81, Num 17, pp 1523-1530, issn 0028-3878, 8 p.Article

Knee bobbing in Charcot-Marie-Tooth diseaseROSSOR, Alexander M; MURPHY, Sinead; REILLY, Mary M et al.Practical neurology (Print). 2012, Vol 12, Num 3, pp 182-183, issn 1474-7758, 2 p.Article

Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsPOLKE, J. M; LAURA, M; DEVILE, C et al.Neurology. 2011, Vol 77, Num 2, pp 168-173, issn 0028-3878, 6 p.Article

POLG1 Mutations Manifesting as Autosomal Recessive Axonal Charcot-Marie-Tooth DiseaseHARROWER, Timothy; STEWART, Joanna D; HUDSON, Gavin et al.Archives of neurology (Chicago). 2008, Vol 65, Num 1, pp 133-136, issn 0003-9942, 4 p.Article

Mutations in TRPV4 cause Charcot-Marie-Tooth disease type 2CLANDOURE, Guida; ZDEBIK, Anselm A; CHOO, Shelly S et al.Nature genetics. 2010, Vol 42, Num 2, pp 170-174, issn 1061-4036, 5 p.Article

La maladie de Charcot-Marie-Tooth = Charcot-Marie-Tooth diseaseBIROUK, Nazha.La Presse médicale (1983). 2009, Vol 38, Num 2, pp 200-209, issn 0755-4982, 10 p.Article

Dynamin 2 mutations in Charcot―Marie―Tooth neuropathy highlight the importance of clathrin-mediated endocytosis in myelinationSIDIROPOULO, Páris N. M; MIEH, Michael; BOCK, Thomas et al.Brain. 2012, Vol 135, pp 1395-1411, issn 0006-8950, 17 p., 5Article

Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutationsCASSEREAU, Julien; CHEVROLLIER, Arnaud; PROCACCIO, Vincent et al.Experimental neurology (Print). 2011, Vol 227, Num 1, pp 31-41, issn 0014-4886, 11 p.Article

Mutation screening of mitofusin 2 in Charcot-Marie-Tooth disease type 2MCCORQUODALE, Donald S; MONTENEGRO, Gladys; PEGUERO, Ainsley et al.Journal of neurology. 2011, Vol 258, Num 7, pp 1234-1239, issn 0340-5354, 6 p.Article

Role of mitofusin 2 mutations in the physiopathology of Charcot―Marie―Tooth disease type 2ACARTONI, Romain; MARTINOU, Jean-Claude.Experimental neurology (Print). 2009, Vol 218, Num 2, pp 268-273, issn 0014-4886, 6 p.Article

Two Novel Mutations in the GDAP1 and PRX Genes in Early Onset Charcot-Marie-Tooth SyndromeAUER-GRUMBACH, M; FISCHER, C; WINDPASSINGER, C et al.Neuropediatrics. 2008, Vol 39, Num 1, pp 33-38, issn 0174-304X, 6 p.Article

Ultrasound-guided peripheral regional blockade in patients with Charcot-Marie-Tooth disease : a review of three casesDHIR, Shalini; BALASUBRAMANIAN, Shyam; ROSS, Douglas et al.Canadian journal of anaesthesia. 2008, Vol 55, Num 8, pp 515-520, issn 0832-610X, 6 p.Article

Genetic dysfunction of MT-A TP6 causes axonal Charcot-Marie-Tooth diseasePITCEATHLY, Robert D. S; MURPHY, Sinéad M; HOLTON, Janice L et al.Neurology. 2012, Vol 79, Num 11, pp 1145-1154, issn 0028-3878, 10 p.Article

A retrospective review of X-linked Charcot-Marie-Tooth disease in childhoodYIU, E. M; GEEVASINGA, N; NICHOLSON, G. A et al.Neurology. 2011, Vol 76, Num 5, pp 461-466, issn 0028-3878, 6 p.Article

Copy number variation upstream of PMP22 in Charcot-Marie-Tooth diseaseWETERMAN, Marian A. J; VAN RUISSEN, Fred; DE WISSEL, Marit et al.European journal of human genetics. 2010, Vol 18, Num 4, pp 421-428, issn 1018-4813, 8 p.Article

Pied de la maladie de Charcot-Marie-ToothWICART, P; BESSE, J.-L.Cahiers d'enseignement de la SOFCOT. 2010, Vol NOV, pp 187-203, issn 0338-3849, 17 p., SUPArticle

Central Nervous System Signs in X-Linked Charcot-Marie-Tooth Disease After HyperventilationSRINIVASAN, Jayasri; LEVENTER, Richard J; KORNBERG, Andrew J et al.Pediatric neurology. 2008, Vol 38, Num 4, pp 293-295, issn 0887-8994, 3 p.Article