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8. Non-hypertrophic familial neuropathy associated with intention tremor. A variety of Charcot-Marie-Tooth disease? Delwaide PJ; Schoenen J J Neurol Sci; 1976 Jan; 27(1):59-69. PubMed ID: 175133 [TBL] [Abstract][Full Text] [Related]
9. The importance of quantitative electron microscopy in studying hypertrophic neuropathies. A comparison between a case of Déjérine Sottas disease (HMSN III) and a case of the hypertrophic form of Charcot-Marie-Tooth disease (HMSN I). Tredici G; Petruccioli-Pizzini MG; Gergely A; Coletti A Int J Tissue React; 1984; 6(3):267-74. PubMed ID: 6090332 [TBL] [Abstract][Full Text] [Related]
11. [Tumor-like transformation of the median nerve in neural muscular atrophy]. Goth D; Ketelsen UP Handchir Mikrochir Plast Chir; 1983 Dec; 15(4):238-40. PubMed ID: 6317529 [TBL] [Abstract][Full Text] [Related]
12. [Ballerina steps, symptom disclosing hypertrophic Charcot-Marie disease with dominant transmission. Value of electrophysiological studies]. Bady B; Chauplannaz G; Brunon AM Rev Neurol (Paris); 1982; 138(11):827-38. PubMed ID: 7167695 [TBL] [Abstract][Full Text] [Related]
13. Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood. Vanasse M; Dubowitz V Muscle Nerve; 1981; 4(1):26-30. PubMed ID: 7231442 [TBL] [Abstract][Full Text] [Related]
14. F-wave conduction velocity in the deep peroneal nerve: Charcot-Marie-Tooth disease and dystrophia myotonica. Panayiotopoulos CP Muscle Nerve; 1978; 1(1):37-44. PubMed ID: 752107 [TBL] [Abstract][Full Text] [Related]
15. Neuromyotonia in the spinal form of Charcot-Marie-Tooth disease. Lance JW; Durke D; Pollard J Clin Exp Neurol; 1979; 16():49-56. PubMed ID: 550956 [TBL] [Abstract][Full Text] [Related]
16. Cardiac findings in Charcot-Marie-Tooth disease. A prospective study of 68 patients. Isner JM; Hawley RJ; Weintraub AM; Engel WK Arch Intern Med; 1979 Oct; 139(10):1161-5. PubMed ID: 485749 [TBL] [Abstract][Full Text] [Related]