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Journal Abstract Search
207 related items for PubMed ID: 1293986
1. [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; 14(4-6):431-9. PubMed ID: 1293986 [Abstract] [Full Text] [Related]
9. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia. Le Ber I, Clot F, Vercueil L, Camuzat A, Viémont M, Benamar N, De Liège P, Ouvrard-Hernandez AM, Pollak P, Stevanin G, Brice A, Dürr A. Neurology; 2006 Nov 28; 67(10):1769-73. PubMed ID: 17130408 [Abstract] [Full Text] [Related]
12. A Japanese family with early-onset ataxia with motor and sensory neuropathy. Kobayashi S, Takuma H, Murayama S, Sakurai M, Kanazawa I. J Neurol Sci; 2007 Mar 15; 254(1-2):44-8. PubMed ID: 17258771 [Abstract] [Full Text] [Related]
19. Neurophysiological study in a Spanish family with recessive spastic ataxia of Charlevoix-Saguenay. García A, Criscuolo C, de Michele G, Berciano J. Muscle Nerve; 2008 Jan 15; 37(1):107-10. PubMed ID: 17683082 [Abstract] [Full Text] [Related]
20. Early onset cerebellar ataxia with retained tendon reflexes (EOCA): an electromyographic study. Pal PK, Taly AB, Nagaraja D, Rao S. Electromyogr Clin Neurophysiol; 1996 Jan 15; 36(5):287-93. PubMed ID: 8877321 [Abstract] [Full Text] [Related] Page: [Next] [New Search]