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

Year Number of Results
1986 1
1987 3
1988 3
1989 6
1990 7
1991 5
1992 1
1993 1
1994 2
1995 3
1996 3
1997 2
1998 4
1999 2
2000 3
2001 7
2002 6
2003 8
2004 7
2005 9
2006 6
2007 9
2008 6
2009 13
2010 5
2011 4
2012 6
2013 9
2014 10
2015 6
2016 4
2017 9
2018 8
2019 8
2020 5
2021 1
2022 5
2023 2
2024 2

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186 results

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Page 1
Mitochondrial encephalomyopathies.
Lombes A, Bonilla E, Dimauro S. Lombes A, et al. Rev Neurol (Paris). 1989;145(10):671-89. Rev Neurol (Paris). 1989. PMID: 2682927 Review.
Unsolved issues related to human mitochondrial diseases.
Lombès A, Auré K, Bellanné-Chantelot C, Gilleron M, Jardel C. Lombès A, et al. Biochimie. 2014 May;100:171-6. doi: 10.1016/j.biochi.2013.08.012. Epub 2013 Aug 20. Biochimie. 2014. PMID: 23973280 Free article. Review.
S100A8-mediated metabolic adaptation controls HIV-1 persistence in macrophages in vivo.
Real F, Zhu A, Huang B, Belmellat A, Sennepin A, Vogl T, Ransy C, Revol M, Arrigucci R, Lombès A, Roth J, Gennaro ML, Bouillaud F, Cristofari S, Bomsel M. Real F, et al. Among authors: lombes a. Nat Commun. 2022 Oct 11;13(1):5956. doi: 10.1038/s41467-022-33401-x. Nat Commun. 2022. PMID: 36220814 Free PMC article.
[Pathophysiology of human mitochondrial diseases].
Lombès A, Auré K, Jardel C. Lombès A, et al. Biol Aujourdhui. 2015;209(2):125-32. doi: 10.1051/jbio/2015014. Epub 2015 Oct 29. Biol Aujourdhui. 2015. PMID: 26514381 Review. French.
Expanding and Underscoring the Hepato-Encephalopathic Phenotype of QIL1/MIC13.
Russell BE, Whaley KG, Bove KE, Labilloy A, Lombardo RC, Hopkin RJ, Leslie ND, Prada C, Assouline Z, Barcia G, Bouchereau J, Chomton M, Debray D, Dorboz I, Durand P, Gaignard P, Habes D, Jardel C, Labarthe F, Lévy J, Lombès A, Mehler-Jacob C, Melki J, Menvielle L, Munnich A, Mussini C, Pichard S, Rio M, Rötig A, Sissaoui S, Slama A, Miethke AG, Schiff M. Russell BE, et al. Among authors: lombes a. Hepatology. 2019 Sep;70(3):1066-1070. doi: 10.1002/hep.30627. Epub 2019 May 16. Hepatology. 2019. PMID: 30912852 Review. No abstract available.
Homoplasmic deleterious MT-ATP6/8 mutations in adult patients.
Rucheton B, Jardel C, Filaut S, Amador MDM, Maisonobe T, Serre I, Romero NB, Leonard-Louis S, Haraux F, Lombès A. Rucheton B, et al. Among authors: lombes a. Mitochondrion. 2020 Nov;55:64-77. doi: 10.1016/j.mito.2020.08.004. Epub 2020 Aug 26. Mitochondrion. 2020. PMID: 32858252
Cytochrome c oxidase deficiency.
DiMauro S, Lombes A, Nakase H, Mita S, Fabrizi GM, Tritschler HJ, Bonilla E, Miranda AF, DeVivo DC, Schon EA. DiMauro S, et al. Among authors: lombes a. Pediatr Res. 1990 Nov;28(5):536-41. doi: 10.1203/00006450-199011000-00025. Pediatr Res. 1990. PMID: 2175026 Review.
186 results