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45. Genetic aspects of hereditary motor and sensory neuropathy (types I and II). Harding AE; Thomas PK J Med Genet; 1980 Oct; 17(5):329-36. PubMed ID: 7218272 [TBL] [Abstract][Full Text] [Related]
46. Neurophysiology and molecular genetics of Charcot-Marie-Tooth type 1 neuropathy in Croatian children: follow-up study. Barisić N; Mihatov I Croat Med J; 2000 Sep; 41(3):306-13. PubMed ID: 10962051 [TBL] [Abstract][Full Text] [Related]
47. Charcot-Marie-Tooth disease with sex-linked inheritance, linkage studies and abnormal serum alkaline phosphatase levels. de Weerdt CJ Eur Neurol; 1978; 17(6):336-44. PubMed ID: 744199 [TBL] [Abstract][Full Text] [Related]
49. Cochlear implantation in a patient with deafness induced by Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathies). Postelmans JT; Stokroos RJ J Laryngol Otol; 2006 Jun; 120(6):508-10. PubMed ID: 16772060 [TBL] [Abstract][Full Text] [Related]
50. [Deafness as a symptom of neural muscular atrophy (Charcot-Marie-Tooth disease)]. Laubert A HNO; 1986 Oct; 34(10):434-7. PubMed ID: 3793530 [TBL] [Abstract][Full Text] [Related]
51. Naevoid basal cell carcinoma syndrome and Charcot-Marie-Tooth disease: two autosomal dominant disorders segregating in a family. Heimler A; Friedman E; Rosenthal AD J Med Genet; 1978 Aug; 15(4):288-91. PubMed ID: 712760 [TBL] [Abstract][Full Text] [Related]
52. [Significance of sibship studies--as demonstrated on a new family with neural muscular atrophy (Charcot-Marie-Tooth)]. Wagner A Z Arztl Fortbild (Jena); 1972 Jun; 66(12):621-4. PubMed ID: 4538352 [No Abstract] [Full Text] [Related]
53. X-linked Charcot-Marie-Tooth disease: phenotypic expression of a novel mutation Ile127Ser in the GJB1 (connexin 32) gene. Vondracek P; Seeman P; Hermanova M; Fajkusova L Muscle Nerve; 2005 Feb; 31(2):252-5. PubMed ID: 15468313 [TBL] [Abstract][Full Text] [Related]