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[Inclusion body myositis. Report of 4 cases].
Medicina (B Aires). 2002;62(1):37-40.
Medicina (B Aires). 2002.
PMID: 11965848
Spanish.
Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).
De Kremer RD, Paschini-Capra A, Bacman S, Argaraña C, Civallero G, Kelley RI, Guelbert N, Latini A, Noher de Halac I, Giner-Ayala A, Johnston J, Proujansky R, Gonzalez I, Depetris-Boldini C, Oller-Ramírez A, Angaroni C, Theaux RA, Hliba E, Juaneda E.
De Kremer RD, et al. Among authors: theaux ra.
Am J Med Genet. 2001 Mar 1;99(2):83-93. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1136>3.0.co;2-x.
Am J Med Genet. 2001.
PMID: 11241464
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Validation of a rabbit model of neuropathy induced by immunization with gangliosides.
Moyano AL, Comín R, Lardone RD, Alaniz ME, Theaux R, Irazoqui FJ, Nores GA.
Moyano AL, et al. Among authors: theaux r.
J Neurol Sci. 2008 Sep 15;272(1-2):110-4. doi: 10.1016/j.jns.2008.05.006. Epub 2008 Jun 24.
J Neurol Sci. 2008.
PMID: 18573503
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[Surgery of intractable epilepsy in infants and adolescents. Case report].
Herrera EJ, Palacios C, Suárez JC, Pueyrredón FJ, Surur A, Theaux R, Suárez MS, Pérez Fonticiella S, Viano JC.
Herrera EJ, et al. Among authors: theaux r.
Arch Argent Pediatr. 2012 Aug;110(4):334-7. doi: 10.5546/aap.2012.334.
Arch Argent Pediatr. 2012.
PMID: 22859329
Free article.
Spanish.
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[Posterior cortical atrophy: anatomo-clinical variant of Alzheimer's disease].
Jacquet MF, Boucquey D, Theaux R, Smidts M, Callewaert A, Brucher JM, Kevers L.
Jacquet MF, et al. Among authors: theaux r.
Acta Neurol Belg. 1990;90(5):265-73.
Acta Neurol Belg. 1990.
PMID: 2085089
French.
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