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2. [Clinical and electrophysiological findings in various hereditary sensory neuropathies]. Caruso G, Santoro L, Perretti A. Acta Neurol (Napoli); 1992; 14(4-6):345-62. PubMed ID: 1293978 [Abstract] [Full Text] [Related]
3. Electrophysiological and pathological studies in spinocerebellar degenerations. McLeod JG, Morgan JA. Proc Aust Assoc Neurol; 1976; 13():113-7. PubMed ID: 1028997 [Abstract] [Full Text] [Related]
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10. [Clinical, multimodal electrophysiological study of a family with progressive cerebellar ataxia and late deafness and an autosomal recessive inheritance]. Ragno M, Curatola L, Rossi R, Salvolini U. Acta Neurol (Napoli); 1992 Jun; 14(4-6):431-9. PubMed ID: 1293986 [Abstract] [Full Text] [Related]
11. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32. Brkanac Z, Fernandez M, Matsushita M, Lipe H, Wolff J, Bird TD, Raskind WH. Am J Med Genet; 2002 May 08; 114(4):450-7. PubMed ID: 11992570 [Abstract] [Full Text] [Related]
12. Peripheral neuropathy in late onset spinocerebellar ataxia. Nousiainen U, Partanen J, Laulumaa V, Paljärvi L. Muscle Nerve; 1988 May 08; 11(5):478-83. PubMed ID: 2836729 [Abstract] [Full Text] [Related]
13. [A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation]. Ohnishi A, Yoshimura T, Takazawa A, Hashimoto T, Yamamoto T, Fukushima Y. Rinsho Shinkeigaku; 1995 Aug 08; 35(8):843-9. PubMed ID: 8665724 [Abstract] [Full Text] [Related]
14. Sensory nerve conduction velocities in forelimb of ponies. Blythe LL, Kitchell RL, Holliday TA, Johnson RD. Am J Vet Res; 1983 Aug 08; 44(8):1419-26. PubMed ID: 6625292 [Abstract] [Full Text] [Related]
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