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.
13. [Hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Molecular-genetic aspects]. Hertz MJ; Jensen AD; Brandt CA; Bisgård C Ugeskr Laeger; 1995 Jun; 157(25):3613-8. PubMed ID: 7652980 [TBL] [Abstract][Full Text] [Related]
14. Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update. Tazir M; Hamadouche T; Nouioua S; Mathis S; Vallat JM J Neurol Sci; 2014 Dec; 347(1-2):14-22. PubMed ID: 25454638 [TBL] [Abstract][Full Text] [Related]
15. [Animal models of Charcot-Marie-Tooth disease and their relevance for understanding the disease in humans]. Bouhy D; Timmerman V Rev Neurol (Paris); 2013 Dec; 169(12):971-7. PubMed ID: 24238786 [TBL] [Abstract][Full Text] [Related]
16. Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations. Chung KW; Kim SB; Park KD; Choi KG; Lee JH; Eun HW; Suh JS; Hwang JH; Kim WK; Seo BC; Kim SH; Son IH; Kim SM; Sunwoo IN; Choi BO Brain; 2006 Aug; 129(Pt 8):2103-18. PubMed ID: 16835246 [TBL] [Abstract][Full Text] [Related]
17. Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy. Briani C; Adami F; Cavallaro T; Taioli F; Ferrari S; Fabrizi G Muscle Nerve; 2008 Jul; 38(1):921-3. PubMed ID: 18563718 [TBL] [Abstract][Full Text] [Related]
18. The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease. Cuesta A; Pedrola L; Sevilla T; García-Planells J; Chumillas MJ; Mayordomo F; LeGuern E; Marín I; Vílchez JJ; Palau F Nat Genet; 2002 Jan; 30(1):22-5. PubMed ID: 11743580 [TBL] [Abstract][Full Text] [Related]
19. [Clinical phenotype of Charcot-Marie-Tooth disease (CMT) and familial amyloid polyneuropathy (FAP)]. Sobue G Rinsho Shinkeigaku; 2003 Nov; 43(11):769-74. PubMed ID: 15152460 [TBL] [Abstract][Full Text] [Related]
20. Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth disease. Tang B; Liu X; Zhao G; Luo W; Xia K; Pan Q; Cai F; Hu Z; Zhang C; Chen B; Zhang F; Shen L; Zhang R; Jiang H Arch Neurol; 2005 Aug; 62(8):1201-7. PubMed ID: 16087758 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]