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

Year Number of Results
1993 1
2002 1
2003 5
2004 1
2005 5
2006 3
2007 9
2008 8
2009 6
2010 11
2011 5
2012 11
2013 9
2014 5
2015 17
2016 17
2017 7
2018 10
2019 12
2020 16
2021 17
2022 15
2023 12
2024 4

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184 results

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Page 1
Glycogen Storage Disease Type V.
Martín MA, Lucia A, Arenas J, Andreu AL. Martín MA, et al. 2006 Apr 19 [updated 2019 Jun 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2006 Apr 19 [updated 2019 Jun 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301518 Free Books & Documents. Review.
Two independent respiratory chains adapt OXPHOS performance to glycolytic switch.
Fernández-Vizarra E, López-Calcerrada S, Sierra-Magro A, Pérez-Pérez R, Formosa LE, Hock DH, Illescas M, Peñas A, Brischigliaro M, Ding S, Fearnley IM, Tzoulis C, Pitceathly RDS, Arenas J, Martín MA, Stroud DA, Zeviani M, Ryan MT, Ugalde C. Fernández-Vizarra E, et al. Among authors: martin ma. Cell Metab. 2022 Nov 1;34(11):1792-1808.e6. doi: 10.1016/j.cmet.2022.09.005. Epub 2022 Oct 4. Cell Metab. 2022. PMID: 36198313 Free article.
When should a nephrologist suspect a mitochondrial disease?
Cavero T, Rabasco C, Molero A, Blázquez A, Hernández E, Martín MA, Praga M. Cavero T, et al. Among authors: martin ma. Nefrologia. 2015;35(1):6-17. doi: 10.3265/Nefrologia.pre2014.Sep.12728. Nefrologia. 2015. PMID: 25611829 Free article. Review. English, Spanish.
Regulation of Mitochondrial Function by the Actin Cytoskeleton.
Illescas M, Peñas A, Arenas J, Martín MA, Ugalde C. Illescas M, et al. Among authors: martin ma. Front Cell Dev Biol. 2021 Dec 21;9:795838. doi: 10.3389/fcell.2021.795838. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34993202 Free PMC article. Review.
Genes and exercise intolerance: insights from McArdle disease.
Nogales-Gadea G, Godfrey R, Santalla A, Coll-Cantí J, Pintos-Morell G, Pinós T, Arenas J, Martín MA, Lucia A. Nogales-Gadea G, et al. Physiol Genomics. 2016 Feb;48(2):93-100. doi: 10.1152/physiolgenomics.00076.2015. Epub 2015 Oct 13. Physiol Genomics. 2016. PMID: 26465709 Review.
Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis.
Domínguez-González C, Fernández-Torrón R, Moore U, de Fuenmayor-Fernández de la Hoz CP, Vélez-Gómez B, Cabezas JA, Alonso-Pérez J, González-Mera L, Olivé M, García-García J, Moris G, León Hernández JC, Muelas N, Servian-Morilla E, Martin MA, Díaz-Manera J, Paradas C. Domínguez-González C, et al. Among authors: martin ma. J Neurol. 2022 Jul;269(7):3550-3562. doi: 10.1007/s00415-021-10957-0. Epub 2022 Mar 14. J Neurol. 2022. PMID: 35286480 Free PMC article.
Exercise and Preexercise Nutrition as Treatment for McArdle Disease.
Nogales-Gadea G, Santalla A, Ballester-Lopez A, Arenas J, Martín MA, Godfrey R, Pinós T, Pintos-Morell G, Coll-Cantí J, Lucia A. Nogales-Gadea G, et al. Med Sci Sports Exerc. 2016 Apr;48(4):673-9. doi: 10.1249/MSS.0000000000000812. Med Sci Sports Exerc. 2016. PMID: 26559449 Review.
Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 deficiency.
Domínguez-González C, Madruga-Garrido M, Hirano M, Martí I, Martín MA, Munell F, Nascimento A, Olivé M, Quan J, Sardina MD, Martí R, Paradas C. Domínguez-González C, et al. Among authors: martin ma. Orphanet J Rare Dis. 2021 Oct 2;16(1):407. doi: 10.1186/s13023-021-02030-w. Orphanet J Rare Dis. 2021. PMID: 34600563 Free PMC article. Review.
184 results