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

Year Number of Results
2002 2
2003 6
2004 6
2005 5
2006 6
2007 3
2008 3
2009 1
2010 2
2011 5
2012 3
2013 2
2014 2
2015 6
2016 9
2017 6
2018 2
2019 5
2020 5
2021 5
2022 5
2023 1
2024 0

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82 results

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Page 1
Nutrition, Bioenergetics, and Metabolic Syndrome.
García-García FJ, Monistrol-Mula A, Cardellach F, Garrabou G. García-García FJ, et al. Among authors: cardellach f. Nutrients. 2020 Sep 11;12(9):2785. doi: 10.3390/nu12092785. Nutrients. 2020. PMID: 32933003 Free PMC article. Review.
CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative.
Luque J, Mendes I, Gómez B, Morte B, López de Heredia M, Herreras E, Corrochano V, Bueren J, Gallano P, Artuch R, Fillat C, Pérez-Jurado LA, Montoliu L, Carracedo Á, Millán JM, Webb SM, Palau F; CIBERER Network; Lapunzina P. Luque J, et al. Clin Genet. 2022 May;101(5-6):481-493. doi: 10.1111/cge.14113. Epub 2022 Feb 4. Clin Genet. 2022. PMID: 35060122 Free PMC article. Review.
Unravelling inclusion body myositis using a patient-derived fibroblast model.
Cantó-Santos J, Valls-Roca L, Tobías E, García-García FJ, Guitart-Mampel M, Esteve-Codina A, Martín-Mur B, Casado M, Artuch R, Solsona-Vilarrasa E, Fernandez-Checa JC, García-Ruiz C, Rentero C, Enrich C, Moreno-Lozano PJ, Milisenda JC, Cardellach F, Grau-Junyent JM, Garrabou G. Cantó-Santos J, et al. Among authors: cardellach f. J Cachexia Sarcopenia Muscle. 2023 Apr;14(2):964-977. doi: 10.1002/jcsm.13178. Epub 2023 Mar 1. J Cachexia Sarcopenia Muscle. 2023. PMID: 36860172 Free PMC article.
Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases.
Bullich G, Matalonga L, Pujadas M, Papakonstantinou A, Piscia D, Tonda R, Artuch R, Gallano P, Garrabou G, González JR, Grinberg D, Guitart M, Laurie S, Lázaro C, Luengo C, Martí R, Milà M, Ovelleiro D, Parra G, Pujol A, Tizzano E, Macaya A, Palau F, Ribes A, Pérez-Jurado LA, Beltran S; Undiagnosed Rare Disease Program of Catalonia (URD-Cat) Consortium. Bullich G, et al. J Mol Diagn. 2022 May;24(5):529-542. doi: 10.1016/j.jmoldx.2022.02.003. J Mol Diagn. 2022. PMID: 35569879 Free article.
Clinical and genetic characterization of the autoinflammatory diseases diagnosed in an adult reference center.
Hernández-Rodríguez J, Ruíz-Ortiz E, Tomé A, Espinosa G, González-Roca E, Mensa-Vilaró A, Prieto-González S, Espígol-Frigolé G, Mensa J, Cardellach F, Grau JM, Cid MC, Yagüe J, Aróstegui JI, Cervera R. Hernández-Rodríguez J, et al. Among authors: cardellach f. Autoimmun Rev. 2016 Jan;15(1):9-15. doi: 10.1016/j.autrev.2015.08.008. Epub 2015 Aug 21. Autoimmun Rev. 2016. PMID: 26299986 Review.
The effects of sepsis on mitochondria.
Garrabou G, Morén C, López S, Tobías E, Cardellach F, Miró O, Casademont J. Garrabou G, et al. Among authors: cardellach f. J Infect Dis. 2012 Feb 1;205(3):392-400. doi: 10.1093/infdis/jir764. Epub 2011 Dec 16. J Infect Dis. 2012. PMID: 22180620
82 results