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

Year Number of Results
1989 1
1991 1
1998 1
2010 1
2011 1
2012 2
2013 4
2014 1
2015 4
2016 1
2017 1
2018 1
2019 1
2020 3
2021 3
2022 1
2023 3
2024 2

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31 results

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Page 1
[Thymomas].
Sánchez Heras AB, Pastor Borgoñón M, López Rodríguez A, Montalar Salcedo J. Sánchez Heras AB, et al. An Med Interna. 1989 Dec;6(12):651-5. An Med Interna. 1989. PMID: 2491478 Review. Spanish.
SEOM clinical guideline on heritable TP53-related cancer syndrome (2022).
Sánchez-Heras AB, Ramon Y Cajal T, Pineda M, Aguirre E, Graña B, Chirivella I, Balmaña J, Brunet J; SEOM Hereditary Cancer Working Group and AEGH Hereditary Cancer Committee. Sánchez-Heras AB, et al. Clin Transl Oncol. 2023 Sep;25(9):2627-2633. doi: 10.1007/s12094-023-03202-9. Epub 2023 May 3. Clin Transl Oncol. 2023. PMID: 37133731 Free PMC article.
Clinical guideline seom: hereditary colorectal cancer.
Guillén-Ponce C, Serrano R, Sánchez-Heras AB, Teulé A, Chirivella I, Martín T, Martínez E, Morales R, Robles L. Guillén-Ponce C, et al. Among authors: sanchez heras ab. Clin Transl Oncol. 2015 Dec;17(12):962-71. doi: 10.1007/s12094-015-1439-z. Epub 2015 Nov 19. Clin Transl Oncol. 2015. PMID: 26586118 Free PMC article.
[Bladder paraganglioma: Report of two cases and a literature review.].
Pelegrín-Mateo FJ, Seguí-Moya E, Fernández-Cruz M, García-Seguí A, De Nova-Sánchez E, Sánchez-Heras AB. Pelegrín-Mateo FJ, et al. Among authors: sanchez heras ab. Arch Esp Urol. 2021 May;74(4):445-449. Arch Esp Urol. 2021. PMID: 33942738 Free article. Review. Spanish.
Co-occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome.
Ferrer-Avargues R, Castillejo MI, Dámaso E, Díez-Obrero V, Garrigos N, Molina T, Codoñer-Alejos A, Segura Á, Sánchez-Heras AB, Castillejo A, Soto JL. Ferrer-Avargues R, et al. Among authors: sanchez heras ab. Cancer Commun (Lond). 2021 Mar;41(3):218-228. doi: 10.1002/cac2.12134. Epub 2021 Feb 25. Cancer Commun (Lond). 2021. PMID: 33630411 Free PMC article.
Characterization of a novel POLD1 missense founder mutation in a Spanish population.
Ferrer-Avargues R, Díez-Obrero V, Martín-Tomás E, Hernández-Illán E, Castillejo MI, Codoñer-Alejos A, Barberá VM, Sánchez-Heras AB, Segura Á, Juan MJ, Tena I, Castillejo A, Soto JL. Ferrer-Avargues R, et al. Among authors: sanchez heras ab. J Gene Med. 2017 Apr;19(4). doi: 10.1002/jgm.2951. J Gene Med. 2017. PMID: 28306219
Use of multi-gene panels in patients at high risk of hereditary digestive cancer: position statement of AEG, SEOM, AEGH and IMPaCT-GENÓMICA consortium.
Carballal S, Balaguer F, Bujanda L, Capellá G, González Santiago S, Jover R, Moreira L, Pineda M, Ruiz-Ponte C, Sánchez Heras AB, Serrano Blanch R, Soto JL, Vidal Tocino R, Cubiella J; en representación de AEG; SEOM; AEGH y consorcio IMPaCT-Genómica. Carballal S, et al. Among authors: sanchez heras ab. Gastroenterol Hepatol. 2024 Mar;47(3):293-318. doi: 10.1016/j.gastrohep.2023.06.004. Epub 2023 Jun 13. Gastroenterol Hepatol. 2024. PMID: 37315767 English, Spanish.
SEOM clinical guideline on hereditary colorectal cancer (2019).
Guillén-Ponce C, Lastra E, Lorenzo-Lorenzo I, Martín Gómez T, Morales Chamorro R, Sánchez-Heras AB, Serrano R, Soriano Rodríguez MC, Soto JL, Robles L. Guillén-Ponce C, et al. Among authors: sanchez heras ab. Clin Transl Oncol. 2020 Feb;22(2):201-212. doi: 10.1007/s12094-019-02272-y. Epub 2020 Jan 24. Clin Transl Oncol. 2020. PMID: 31981079 Free article.
Laboratory Cross-Comparison and Ring Test Trial for Tumor BRCA Testing in a Multicenter Epithelial Ovarian Cancer Series: The BORNEO GEICO 60-0 Study.
Garcia-Casado Z, Oaknin A, Mendiola M, Alkorta-Aranburu G, Antunez-Lopez JR, Moreno-Bueno G, Palacios J, Yubero A, Marquez R, Gallego A, Sanchez-Heras AB, Lopez-Guerrero JA, Perez-Segura C, Barretina-Ginesta P, Alarcon J, Gaba L, Marquez A, Matito J, Cueva J, Palacio I, Iglesias M, Arcusa A, Sanchez-Lorenzo L, Guerra-Alia E, Romero I, Vivancos A. Garcia-Casado Z, et al. Among authors: sanchez heras ab. J Pers Med. 2022 Nov 4;12(11):1842. doi: 10.3390/jpm12111842. J Pers Med. 2022. PMID: 36579549 Free PMC article.
31 results