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

Year Number of Results
1992 1
2002 1
2003 2
2004 2
2005 2
2007 4
2008 3
2009 2
2010 3
2011 2
2012 1
2013 1
2014 8
2015 5
2016 6
2017 4
2018 6
2019 11
2020 6
2021 11
2022 8
2023 6
2024 3

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87 results

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Page 1
Standards of care for patients with spondyloarthritis.
Abad MÁ, Ariza RA, Aznar JJ, Batlle E, Beltrán E, de Dios Cañete J, de Miguel E, Escudero A, Fernández-Carballido C, Gratacós J, Loza E, Linares LF, Montilla C, Ramos MM, Mulero J, Queiro R, Raya E, Lozano CR, Moreno JR, Sanz J, Silva-Fernández L, Torre Alonso JC, Zarco P, Fernández-Sueiro JL, Juanola X; 2e study group; Spanish Society of Rheumatology. Abad MÁ, et al. Rheumatol Int. 2014 Feb;34(2):165-70. doi: 10.1007/s00296-013-2934-6. Epub 2014 Jan 4. Rheumatol Int. 2014. PMID: 24390635 Review.
Common recessive limb girdle muscular dystrophies differential diagnosis: why and how?
Cotta A, Carvalho E, da-Cunha-Júnior AL, Paim JF, Navarro MM, Valicek J, Menezes MM, Nunes SV, Xavier Neto R, Takata RI, Vargas AP. Cotta A, et al. Among authors: vargas ap. Arq Neuropsiquiatr. 2014 Sep;72(9):721-34. doi: 10.1590/0004-282x20140110. Arq Neuropsiquiatr. 2014. PMID: 25252238 Free article. Review.
Varón de 35 años con sordera neurosensorial y queratitis intersticial.
Tutor-Ureta P, Yebra-Bango M, Mellor-Pita S, García Berrocal JR, Fernández A, Antonio Vargas J. Tutor-Ureta P, et al. Among authors: antonio vargas j. Reumatol Clin. 2007 May;3(3):144-5. doi: 10.1016/S1699-258X(07)73683-5. Epub 2008 Dec 29. Reumatol Clin. 2007. PMID: 21794418 Free article. Spanish. No abstract available.
Central Core Disease: Facial Weakness Differentiating Biallelic from Monoallelic Forms.
Cotta A, Souza LS, Carvalho E, Feitosa LN, Cunha A Jr, Navarro MM, Valicek J, Menezes MM, Neves SVN, Xavier-Neto R, Vargas AP, Takata RI, Paim JF, Vainzof M. Cotta A, et al. Among authors: vargas ap. Genes (Basel). 2022 Apr 26;13(5):760. doi: 10.3390/genes13050760. Genes (Basel). 2022. PMID: 35627144 Free PMC article.
Phenotypic Variability of Dystrophinopathy Symptomatic Female Carriers.
Cotta A, Paim JF, Carvalho E, Navarro MM, Valicek J, da-Cunha-Junior AL, Menezes MM, Nunes SV, Xavier-Neto R, da Silveira EB, Costa-E-Silva C, Takata RI, Vargas AP. Cotta A, et al. Among authors: vargas ap. Can J Neurol Sci. 2017 May;44(3):304-310. doi: 10.1017/cjn.2016.448. Epub 2017 Feb 9. Can J Neurol Sci. 2017. PMID: 28181471
LMNA-Related Muscular Dystrophy with Clinical Intrafamilial Variability.
Cotta A, Paim JF, Carvalho E, Valicek J, da Cunha Junior AL, Navarro MM, Vargas AP, Lima MI, de Almeida CF, Takata RI, Vainzof M. Cotta A, et al. Among authors: vargas ap. J Mol Neurosci. 2019 Dec;69(4):623-627. doi: 10.1007/s12031-019-01390-0. Epub 2019 Aug 13. J Mol Neurosci. 2019. PMID: 31410651
87 results