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

Year Number of Results
2002 1
2003 1
2006 1
2011 2
2012 2
2013 2
2014 1
2015 2
2016 1
2017 3
2018 2
2019 1
2020 1
2022 2
2023 2
2024 0

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20 results

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Page 1
Nationwide genetic analysis of more than 600 families with inherited eye diseases in Argentina.
Schlottmann PG, Luna JD, Labat N, Yadarola MB, Bainttein S, Esposito E, Ibañez A, Barbaro EI, Álvarez Mendiara A, Picotti CP, Chirino Misisian A, Andreussi L, Gras J, Capalbo L, Visotto M, Dipierri JE, Alcoba E, Fernández Gabrielli L, Ávila S, Aucar ME, Martin DM, Ormaechea GJ, Inga ME, Francone AA, Charles M, Zompa T, Pérez PJ, Lotersztein V, Nuova PJ, Canonero IB, Mahroo OA, Michaelides M, Arno G, Daich Varela M. Schlottmann PG, et al. Among authors: avila s. NPJ Genom Med. 2023 May 22;8(1):8. doi: 10.1038/s41525-023-00352-1. NPJ Genom Med. 2023. PMID: 37217489 Free PMC article.
Human endometrial receptivity: gene regulation.
Martín J, Domínguez F, Avila S, Castrillo JL, Remohí J, Pellicer A, Simón C. Martín J, et al. Among authors: avila s. J Reprod Immunol. 2002 May-Jun;55(1-2):131-9. doi: 10.1016/s0165-0378(01)00140-1. J Reprod Immunol. 2002. PMID: 12062828
PALB2 germline mutations in a multi-gene panel testing cohort of 1905 breast-ovarian cancer patients in Argentina.
Gonzalez A, Del Greco F, Vargas-Roig L, Brun B, Tabares G, Mampel A, Montes C, Martin C, Lopez M, Rossi N, Bruno L, Ponce C, Quaglio P, Yanzi A, Acevedo S, Lugo L, Lopez Breccia P, Avila S, Sisterna S, Del Castillo MS, Vazquez M, Nuñez LM. Gonzalez A, et al. Among authors: avila s. Breast Cancer Res Treat. 2022 Jul;194(2):403-412. doi: 10.1007/s10549-022-06620-5. Epub 2022 May 24. Breast Cancer Res Treat. 2022. PMID: 35610400
Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects.
Delea M, Espeche LD, Bruque CD, Bidondo MP, Massara LS, Oliveri J, Brun P, Cosentino VR, Martinoli C, Tolaba N, Picon C, Ponce Zaldua ME, Ávila S, Gutnisky V, Perez M, Furforo L, Buzzalino ND, Liascovich R, Groisman B, Rittler M, Rozental S, Barbero P, Dain L. Delea M, et al. Among authors: avila s. Genes (Basel). 2018 Sep 11;9(9):454. doi: 10.3390/genes9090454. Genes (Basel). 2018. PMID: 30208644 Free PMC article.
RENAC: National Registry of Congenital Anomalies of Argentina.
Groisman B, Bidondo MP, Barbero P, Gili JA, Liascovich R; RENAC Task Force. Groisman B, et al. Arch Argent Pediatr. 2013 Dec;111(6):484-94. doi: 10.5546/aap.2013.eng.484. Arch Argent Pediatr. 2013. PMID: 24196761 Free article. English, Spanish.
iPSC-Derived Intestinal Organoids from Cystic Fibrosis Patients Acquire CFTR Activity upon TALEN-Mediated Repair of the p.F508del Mutation.
Fleischer A, Vallejo-Díez S, Martín-Fernández JM, Sánchez-Gilabert A, Castresana M, Del Pozo A, Esquisabel A, Ávila S, Castrillo JL, Gaínza E, Pedraz JL, Viñas M, Bachiller D. Fleischer A, et al. Among authors: avila s. Mol Ther Methods Clin Dev. 2020 Apr 18;17:858-870. doi: 10.1016/j.omtm.2020.04.005. eCollection 2020 Jun 12. Mol Ther Methods Clin Dev. 2020. PMID: 32373648 Free PMC article.
20 results