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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?
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
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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
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Geographical analysis of the sporadic Creutzfeldt-Jakob disease distribution in the autonomous community of the Basque Country for the period 1995-2008.
Chamosa S, Tamayo I, Arteagoitia-Axpe JM, Juste RA, Rodríguez-Martínez AB, Zarranz-Imirizaldu JJ, Arriola L.
Chamosa S, et al. Among authors: rodriguez martinez ab.
Eur Neurol. 2014;72(1-2):20-5. doi: 10.1159/000358298. Epub 2014 May 8.
Eur Neurol. 2014.
PMID: 24819667
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