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4. Variation of phenotype in Charcot-Marie-Tooth disease. Baker RS; Upton AR Neuropadiatrie; 1979 Aug; 10(3):290-5. PubMed ID: 583067 [TBL] [Abstract][Full Text] [Related]
5. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy. McLeod JG; Low PA; Morgan JA Proc Aust Assoc Neurol; 1975; 12():23-5. PubMed ID: 1215391 [TBL] [Abstract][Full Text] [Related]
6. Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33. LeGuern E; Guilbot A; Kessali M; Ravisé N; Tassin J; Maisonobe T; Grid D; Brice A Hum Mol Genet; 1996 Oct; 5(10):1685-8. PubMed ID: 8894708 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Charcot-Marie-Tooth disease with Leber optic atrophy. McLeod JG; Low PA; Morgan JA Neurology; 1978 Feb; 28(2):179-84. PubMed ID: 563998 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Charcot-Marie-Tooth disease: data for genetic counseling relating age to risk. Bird TD; Kraft GH Clin Genet; 1978 Jul; 14(1):43-9. PubMed ID: 679521 [TBL] [Abstract][Full Text] [Related]
11. Palmoplantar keratoderma and Charcot-Marie-Tooth disease. Rabbiosi G; Borroni G; Pinelli P; Cosi V Arch Dermatol; 1980 Jul; 116(7):789-90. PubMed ID: 6446889 [TBL] [Abstract][Full Text] [Related]
12. HLA in Charcot-Marie-Tooth disease. Williams LL Ann Neurol; 1980 Oct; 8(4):452. PubMed ID: 7436389 [No Abstract] [Full Text] [Related]
14. Linkage relations of locus for X-borne type of Charcot-Marie-Tooth muscular atrophy and that for Xg blood groups. de Weerdt CJ J Med Genet; 1976 Oct; 13(5):399. PubMed ID: 1003451 [TBL] [Abstract][Full Text] [Related]
15. Hereditary angioneurotic edema and Charcot-Marie-Tooth disease in the same family. Fernandez PG; Day JH; Simpson NE; Zachariah PK Can Med Assoc J; 1978 Sep; 119(5):455-8. PubMed ID: 688147 [TBL] [Abstract][Full Text] [Related]
16. [Brothers affected by the Charcot-Marie-Tooth peroneal muscular atrophy with a positive variant of the anticipation phenomenon]. Gonçalves A; da Salva JB Arq Neuropsiquiatr; 1977 Jun; 35(2):167-71. PubMed ID: 869740 [TBL] [Abstract][Full Text] [Related]