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Germline heterozygous exons 8-11 pathogenic BARD1 gene deletion reported for the first time in a family with suspicion of a hereditary colorectal cancer syndrome: more than an incidental finding?
Carrera S, Rodríguez-Martínez AB, Garin I, Sarasola E, Martínez C, Maortua H, Callejo A, Ruiz de Lobera A, Muñoz A, Miñambres N, Jiménez-Labaig P. Carrera S, et al. Among authors: rodriguez martinez ab. Hered Cancer Clin Pract. 2023 Jan 28;21(1):2. doi: 10.1186/s13053-023-00246-4. Hered Cancer Clin Pract. 2023. PMID: 36709314 Free PMC article.
A novel PRNP Y218N mutation in Gerstmann-Sträussler-Scheinker disease with neurofibrillary degeneration.
Alzualde A, Indakoetxea B, Ferrer I, Moreno F, Barandiaran M, Gorostidi A, Estanga A, Ruiz I, Calero M, van Leeuwen FW, Atares B, Juste R, Rodriguez-Martínez AB, López de Munain A. Alzualde A, et al. Among authors: rodriguez martinez ab. J Neuropathol Exp Neurol. 2010 Aug;69(8):789-800. doi: 10.1097/NEN.0b013e3181e85737. J Neuropathol Exp Neurol. 2010. PMID: 20613639
5-Hydroxytryptamine 6 receptor (5-HT(6)) receptor and apolipoprotein E (ApoE) polymorphisms in patients with Alzheimer's disease in the Basque Country.
Alvarez-Alvarez M, Galdos L, Fernández-Martínez M, Gómez-Busto F, García-Centeno V, Arias-Arias C, Sánchez-Salazar C, Rodríguez-Martínez AB, Zarranz JJ, de Pancorbo MM. Alvarez-Alvarez M, et al. Among authors: rodriguez martinez ab. Neurosci Lett. 2003 Mar 13;339(1):85-7. doi: 10.1016/s0304-3940(02)01425-8. Neurosci Lett. 2003. PMID: 12618306