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6. Charcot-Marie-Tooth disease associated with hypertrophic neuropathy: a neuropathologic study of two cases. Smith TW; Bhawan J; Keller RB; DeGirolami U J Neuropathol Exp Neurol; 1980 Jul; 39(4):420-40. PubMed ID: 6260904 [TBL] [Abstract][Full Text] [Related]
10. Ultrastructural and cytochemical observations in a case of dominantly inherited hypertrophic (Charcot-Marie-Tooth) neuropathy. Waxman SG; Ouelette EM J Neuropathol Exp Neurol; 1979 Nov; 38(6):586-95. PubMed ID: 533859 [TBL] [Abstract][Full Text] [Related]
11. [Charcot-Marie-Tooth disease. Study of sural nerve biopsy in 41 patients]. Freitas MR; Nascimento OJ; Chimelli L; de Freitas GR Arq Neuropsiquiatr; 1995 Sep; 53(3-B):560-9. PubMed ID: 8585811 [TBL] [Abstract][Full Text] [Related]
12. The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classification. Davis CJ; Bradley WG; Madrid R J Genet Hum; 1978 Dec; 26(4):311-49. PubMed ID: 752065 [TBL] [Abstract][Full Text] [Related]
13. Progressive peroneal muscular atrophy (Charcot-Marie-Tooth disease) associated with beta-thalassemia trait and glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. A clinical and nerve biopsy case. Inzitari D; Rizzuto N; Antuono P; Sità D Ital J Neurol Sci; 1981 Aug; 2(3):269-74. PubMed ID: 7341549 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Variability in nerve biopsy findings in a kinship with dominantly inherited Charcot-Marie-Tooth disease. Van Weerden TW; Houthoff HJ; Sie O; Minderhoud JM Muscle Nerve; 1982 Mar; 5(3):185-96. PubMed ID: 7088015 [No Abstract] [Full Text] [Related]
16. Dynamic aspects of peripheral nerve changes in progressive neural muscular atrophy: light- and electronmicroscopic studies of serial nerve biopsies. Meier C; Maibach R; Isler W; Bischoff A J Neurol; 1976 Jan; 211(2):111-24. PubMed ID: 55467 [TBL] [Abstract][Full Text] [Related]
17. [The nosological situation of hereditary motor and sensory neuropathies (HMSN, Charcot-Marie-Tooth disease, neural muscular atrophy)]. Warzok R; Wattig B; Schwesinger G; Schneeweiss H; Heydenreich F Zentralbl Allg Pathol; 1990; 136(6):549-62. PubMed ID: 2281721 [TBL] [Abstract][Full Text] [Related]
18. Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography. Buchthal F; Behse F Brain; 1977 Mar; 100 Pt 1():41-66. PubMed ID: 861715 [No Abstract] [Full Text] [Related]
19. Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene. Sevilla T; Cuesta A; Chumillas MJ; Mayordomo F; Pedrola L; Palau F; Vílchez JJ Brain; 2003 Sep; 126(Pt 9):2023-33. PubMed ID: 12821518 [TBL] [Abstract][Full Text] [Related]