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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
180 related items for PubMed ID: 6317809
21. 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 [Abstract] [Full Text] [Related]
23. Charcot-Marie-Tooth disease associated with 'essential tremor' and normal and/or slightly diminished motor conduction velocity. Report of 7 cases. Salisachs P, Codina A, Gimenez-Roldan S, Zarranz JJ. Eur Neurol; 1979 Dec; 18(1):49-58. PubMed ID: 436863 [Abstract] [Full Text] [Related]
24. 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]
26. Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with charcot-marie-tooth disease 1A duplication. Berciano J, García A, Calleja J, Combarros O. Neuromuscul Disord; 2000 Aug; 10(6):419-24. PubMed ID: 10899448 [Abstract] [Full Text] [Related]
27. Peroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindred. Frith JA, McLeod JG, Nicholson GA, Yang F. J Neurol Neurosurg Psychiatry; 1994 Nov; 57(11):1343-6. PubMed ID: 7964809 [Abstract] [Full Text] [Related]