These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Genotype/phenotype correlations in X-linked dominant Charcot-Marie-Tooth disease. Hahn AF; Bolton CF; White CM; Brown WF; Tuuha SE; Tan CC; Ainsworth PJ Ann N Y Acad Sci; 1999 Sep; 883():366-82. PubMed ID: 10586261 [TBL] [Abstract][Full Text] [Related]
6. Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review. Berciano J; García A; Gallardo E; Peeters K; Pelayo-Negro AL; Álvarez-Paradelo S; Gazulla J; Martínez-Tames M; Infante J; Jordanova A J Neurol; 2017 Aug; 264(8):1655-1677. PubMed ID: 28364294 [TBL] [Abstract][Full Text] [Related]
7. A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype. De Jonghe P; Timmerman V; Nelis E; De Vriendt E; Löfgren A; Ceuterick C; Martin JJ; Van Broeckhoven C Arch Neurol; 1999 Oct; 56(10):1283-8. PubMed ID: 10520946 [TBL] [Abstract][Full Text] [Related]
8. Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease. Lee MJ; Nelson I; Houlden H; Sweeney MG; Hilton-Jones D; Blake J; Wood NW; Reilly MM J Neurol Neurosurg Psychiatry; 2002 Sep; 73(3):304-6. PubMed ID: 12185164 [TBL] [Abstract][Full Text] [Related]
9. Unusual electrophysiological findings in X-linked dominant Charcot-Marie-Tooth disease. Gutierrez A; England JD; Sumner AJ; Ferer S; Warner LE; Lupski JR; Garcia CA Muscle Nerve; 2000 Feb; 23(2):182-8. PubMed ID: 10639608 [TBL] [Abstract][Full Text] [Related]
10. X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations(1). Senderek J; Hermanns B; Bergmann C; Boroojerdi B; Bajbouj M; Hungs M; Ramaekers VT; Quasthoff S; Karch D; Schröder JM J Neurol Sci; 1999 Aug; 167(2):90-101. PubMed ID: 10521546 [TBL] [Abstract][Full Text] [Related]
11. Slowing of central conduction in X-linked Charcot-Marie-Tooth neuropathy shown by brain stem auditory evoked responses. Nicholson G; Corbett A J Neurol Neurosurg Psychiatry; 1996 Jul; 61(1):43-6. PubMed ID: 8676158 [TBL] [Abstract][Full Text] [Related]
12. Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation. Capasso M; Di Muzio A; Ferrarini M; De Angelis MV; Caporale CM; Lupo S; Cavallaro T; Fabrizi GM; Uncini A Clin Neurophysiol; 2004 Jan; 115(1):64-70. PubMed ID: 14706470 [TBL] [Abstract][Full Text] [Related]
13. Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families. Rouger H; LeGuern E; Birouk N; Gouider R; Tardieu S; Plassart E; Gugenheim M; Vallat JM; Louboutin JP; Bouche P; Agid Y; Brice A Hum Mutat; 1997; 10(6):443-52. PubMed ID: 9401007 [TBL] [Abstract][Full Text] [Related]
14. [Molecular basis of Charcot-Marie-Tooth neuropathy]. Hayasaka K Nihon Rinsho; 1996 Aug; 54(8):2243-51. PubMed ID: 8810804 [TBL] [Abstract][Full Text] [Related]
15. Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy associated with a segmental duplication of chromosome 17. Kaku DA; Parry GJ; Malamut R; Lupski JR; Garcia CA Neurology; 1993 Sep; 43(9):1806-8. PubMed ID: 8414036 [TBL] [Abstract][Full Text] [Related]
16. Penetrance of the hereditary motor and sensory neuropathy Ia mutation: assessment by nerve conduction studies. Nicholson GA Neurology; 1991 Apr; 41(4):547-52. PubMed ID: 2011255 [TBL] [Abstract][Full Text] [Related]
17. Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with central conduction slowing. Seeman P; Mazanec R; Ctvrtecková M; Smilková D Int J Mol Med; 2001 Oct; 8(4):461-8. PubMed ID: 11562788 [TBL] [Abstract][Full Text] [Related]
18. Electrophysiological characterization of Charcot-Marie-Tooth disease type 1A in Taiwan. Huang LW; Lin KP; Chang MH; Liao YC; Liao KK; Soong BW; Lee YC J Chin Med Assoc; 2012 May; 75(5):197-202. PubMed ID: 22632984 [TBL] [Abstract][Full Text] [Related]