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Erratum to: Frequency of germline DNA genetic findings in an unselected prospective cohort of triple-negative breast cancer patients participating in a platinum-based neoadjuvant chemotherapy trial.
González-Rivera M, Lobo M, López-Tarruella S, Jerez Y, Del Monte-Millán M, Massarrah T, Ramos-Medina R, Ocaña I, Picornell A, Santillán Garzón S, Pérez-Carbornero L, García-Saenz JA, Gómez H, Moreno F, Márquez-Rodas I, Fuentes H, Martin M. González-Rivera M, et al. Among authors: santillan garzon s. Breast Cancer Res Treat. 2017 Sep;165(2):471. doi: 10.1007/s10549-017-4396-0. Breast Cancer Res Treat. 2017. PMID: 28721639 No abstract available.
Frequency of germline DNA genetic findings in an unselected prospective cohort of triple-negative breast cancer patients participating in a platinum-based neoadjuvant chemotherapy trial.
González-Rivera M, Lobo M, López-Tarruella S, Jerez Y, Del Monte-Millán M, Massarrah T, Ramos-Medina R, Ocaña I, Picornell A, Santillán Garzón S, Pérez-Carbornero L, García-Saenz JA, Gómez H, Moreno F, Márquez-Rodas I, Fuentes H, Martin M. González-Rivera M, et al. Among authors: santillan garzon s. Breast Cancer Res Treat. 2016 Apr;156(3):507-515. doi: 10.1007/s10549-016-3792-1. Epub 2016 Apr 15. Breast Cancer Res Treat. 2016. PMID: 27083178
Almost 2% of Spanish breast cancer families are associated to germline pathogenic mutations in the ATM gene.
Tavera-Tapia A, Pérez-Cabornero L, Macías JA, Ceballos MI, Roncador G, de la Hoya M, Barroso A, Felipe-Ponce V, Serrano-Blanch R, Hinojo C, Miramar-Gallart MD, Urioste M, Caldés T, Santillan-Garzón S, Benitez J, Osorio A. Tavera-Tapia A, et al. Among authors: santillan garzon s. Breast Cancer Res Treat. 2017 Feb;161(3):597-604. doi: 10.1007/s10549-016-4058-7. Epub 2016 Dec 2. Breast Cancer Res Treat. 2017. PMID: 27913932
Alport Syndrome: De Novo Mutation in the COL4A5 Gene Converting Glycine 1205 to Valine.
Antón-Martín P, Aparicio López C, Ramiro-León S, Santillán Garzón S, Santos-Simarro F, Gil-Fournier B. Antón-Martín P, et al. Among authors: santillan garzon s. Clin Med Insights Pediatr. 2012 Jun 28;6:41-9. doi: 10.2147/CBF.S23366. Print 2012. Clin Med Insights Pediatr. 2012. PMID: 23641165 Free PMC article.
Adolescent with Alport syndrome and congenital hemolytic anemia.
García Maset L, Santillán Garzón S, Ortega López P. García Maset L, et al. Among authors: santillan garzon s. Nefrologia (Engl Ed). 2023 Jan-Feb;43(1):146-147. doi: 10.1016/j.nefroe.2023.03.005. Epub 2023 Mar 28. Nefrologia (Engl Ed). 2023. PMID: 36997470 Free article. No abstract available.
Adolescent with Alport syndrome and congenital hemolytic anemia.
García Maset L, Santillán Garzón S, Ortega López P. García Maset L, et al. Among authors: santillan garzon s. Nefrologia (Engl Ed). 2021 Jun 19:S0211-6995(21)00106-5. doi: 10.1016/j.nefro.2021.05.002. Online ahead of print. Nefrologia (Engl Ed). 2021. PMID: 34158190 Free article. English, Spanish. No abstract available.