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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2004 1
2005 1
2006 1
2007 1
2009 1
2010 2
2012 5
2013 6
2014 1
2015 1
2016 5
2017 8
2018 4
2019 2
2020 2
2021 3
2022 1
2023 4
2024 0

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41 results

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Page 1
MPV17 Mutations Are Associated With a Quiescent Energetic Metabolic Profile.
Jacinto S, Guerreiro P, de Oliveira RM, Cunha-Oliveira T, Santos MJ, Grazina M, Rego AC, Outeiro TF. Jacinto S, et al. Among authors: grazina m. Front Cell Neurosci. 2021 Mar 17;15:641264. doi: 10.3389/fncel.2021.641264. eCollection 2021. Front Cell Neurosci. 2021. PMID: 33815063 Free PMC article.
Genomic Ancestry, CYP2D6, CYP2C9, and CYP2C19 Among Latin Americans.
Rodrigues-Soares F, Peñas-Lledó EM, Tarazona-Santos E, Sosa-Macías M, Terán E, López-López M, Rodeiro I, Moya GE, Calzadilla LR, Ramírez-Roa R, Grazina M, Estévez-Carrizo FE, Barrantes R, LLerena A; RIBEF Ibero-American Network of Pharmacogenetics and Pharmacogenomics. Rodrigues-Soares F, et al. Among authors: grazina m. Clin Pharmacol Ther. 2020 Jan;107(1):257-268. doi: 10.1002/cpt.1598. Epub 2019 Oct 7. Clin Pharmacol Ther. 2020. PMID: 31376146
Diversities in Leigh Syndrome Associated with MT-ATP6 Gene Variants.
Martins S, Santos MJ, Simões M, Jacinto S, Martins Halpern C, Dupont J, Diogo L, Grazina M. Martins S, et al. Among authors: grazina m. Endocr Metab Immune Disord Drug Targets. 2023 Oct 4. doi: 10.2174/0118715303273271230928060000. Online ahead of print. Endocr Metab Immune Disord Drug Targets. 2023. PMID: 37817524
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: grazina m. 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
Frontotemporal dementia and mitochondrial DNA transitions.
Grazina M, Silva F, Santana I, Santiago B, Mendes C, Simões M, Oliveira M, Cunha L, Oliveira C. Grazina M, et al. Neurobiol Dis. 2004 Mar;15(2):306-11. doi: 10.1016/j.nbd.2003.11.004. Neurobiol Dis. 2004. PMID: 15006700 Free article.
Coenzyme Q₁₀ deficiency in mitochondrial DNA depletion syndromes.
Montero R, Grazina M, López-Gallardo E, Montoya J, Briones P, Navarro-Sastre A, Land JM, Hargreaves IP, Artuch R; Coenzyme Q₁₀ Deficiency Study Group. Montero R, et al. Among authors: grazina m. Mitochondrion. 2013 Jul;13(4):337-41. doi: 10.1016/j.mito.2013.04.001. Epub 2013 Apr 11. Mitochondrion. 2013. PMID: 23583954
41 results