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Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients.
Silveira I, Lopes-Cendes I, Kish S, Maciel P, Gaspar C, Coutinho P, Botez MI, Teive H, Arruda W, Steiner CE, Pinto-Júnior W, Maciel JA, Jerin S, Sack G, Andermann E, Sudarsky L, Rosenberg R, MacLeod P, Chitayat D, Babul R, Sequeiros J, Rouleau GA. Silveira I, et al. Among authors: botez mi. Neurology. 1996 Jan;46(1):214-8. doi: 10.1212/wnl.46.1.214. Neurology. 1996. PMID: 8559378
Thiamine status in inherited degenerative ataxias.
Pedraza OL, Botez MI. Pedraza OL, et al. Among authors: botez mi. J Neurol Neurosurg Psychiatry. 1992 Feb;55(2):136-7. doi: 10.1136/jnnp.55.2.136. J Neurol Neurosurg Psychiatry. 1992. PMID: 1538220 Free PMC article.
Cognitive behavior in heredodegenerative ataxias.
Botez-Marquard T, Botez MI. Botez-Marquard T, et al. Among authors: botez mi. Eur Neurol. 1993;33(5):351-7. doi: 10.1159/000116970. Eur Neurol. 1993. PMID: 8243509
Cerebellar atrophy in epileptic patients.
Botez MI, Attig E, Vézina JL. Botez MI, et al. Can J Neurol Sci. 1988 Aug;15(3):299-303. doi: 10.1017/s0317167100027785. Can J Neurol Sci. 1988. PMID: 3208214
145 results