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Antenatal manifestations of mitochondrial disorders.
Tavares MV, Santos MJ, Domingues AP, Pratas J, Mendes C, Simões M, Moura P, Diogo L, Grazina M. Tavares MV, et al. Among authors: pratas j. J Inherit Metab Dis. 2013 Sep;36(5):805-11. doi: 10.1007/s10545-012-9567-x. Epub 2013 Jan 30. J Inherit Metab Dis. 2013. PMID: 23361304
Mitochondrial-dependent apoptosis in Huntington's disease human cybrids.
Ferreira IL, Nascimento MV, Ribeiro M, Almeida S, Cardoso SM, Grazina M, Pratas J, Santos MJ, Januário C, Oliveira CR, Rego AC. Ferreira IL, et al. Among authors: pratas j. Exp Neurol. 2010 Apr;222(2):243-55. doi: 10.1016/j.expneurol.2010.01.002. Epub 2010 Jan 14. Exp Neurol. 2010. PMID: 20079354
Genetic basis of Alzheimer's dementia: role of mtDNA mutations.
Grazina M, Pratas J, Silva F, Oliveira S, Santana I, Oliveira C. Grazina M, et al. Among authors: pratas j. Genes Brain Behav. 2006;5 Suppl 2:92-107. doi: 10.1111/j.1601-183X.2006.00225.x. Genes Brain Behav. 2006. PMID: 16681804 Free article. Review.
Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant.
Bacalhau M, Simões M, Rocha MC, Hardy SA, Vincent AE, Durães J, Macário MC, Santos MJ, Rebelo O, Lopes C, Pratas J, Mendes C, Zuzarte M, Rego AC, Girão H, Wong LC, Taylor RW, Grazina M. Bacalhau M, et al. Among authors: pratas j. Neuromuscul Disord. 2018 Apr;28(4):350-360. doi: 10.1016/j.nmd.2017.11.006. Epub 2017 Nov 23. Neuromuscul Disord. 2018. PMID: 29398297 Free PMC article.
58 results