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

Year Number of Results
1985 1
1993 1
1994 1
1996 2
1999 5
2000 2
2001 1
2002 1
2003 2
2004 3
2005 2
2006 1
2007 5
2008 2
2009 2
2010 2
2011 2
2012 2
2013 4
2014 3
2015 1
2016 1
2017 8
2018 6
2019 6
2020 4
2021 2
2022 1
2023 2
2024 0

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69 results

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Page 1
A Novel C-C Chemoattractant Cytokine (Chemokine) Receptor 6 (CCR6) Antagonist (PF-07054894) Distinguishes between Homologous Chemokine Receptors, Increases Basal Circulating CCR6+ T Cells, and Ameliorates Interleukin-23-Induced Skin Inflammation.
Li W, Crouse KK, Alley J, Frisbie RK, Fish SC, Andreyeva TA, Reed LA, Thorn M, DiMaggio G, Donovan CB, Bennett D, Garren J, Oziolor E, Qian J, Newman L, Vargas AP, Kumpf SW, Steyn SJ, Schnute ME, Thorarensen A, Hegen M, Stevens E, Collinge M, Lanz TA, Vincent F, Vincent MS, Berstein G. Li W, et al. Among authors: vargas ap. J Pharmacol Exp Ther. 2023 Jul;386(1):80-92. doi: 10.1124/jpet.122.001452. Epub 2023 May 4. J Pharmacol Exp Ther. 2023. PMID: 37142443
Persistent Sydenham's chorea.
Cardoso F, Vargas AP, Oliveira LD, Guerra AA, Amaral SV. Cardoso F, et al. Among authors: vargas ap. Mov Disord. 1999 Sep;14(5):805-7. doi: 10.1002/1531-8257(199909)14:5<805::aid-mds1013>3.0.co;2-p. Mov Disord. 1999. PMID: 10495042
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.
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
Unusual early-onset Huntingtons disease.
Vargas AP, Carod-Artal FJ, Bomfim D, Vázquez-Cabrera C, Dantas-Barbosa C. Vargas AP, et al. J Child Neurol. 2003 Jun;18(6):429-32. doi: 10.1177/08830738030180061301. J Child Neurol. 2003. PMID: 12886981
69 results