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Page 1
Undescribed mutations in FBN1 gene in two family cases of Marfan syndrome.
Cabrera-Bueno F, Fernandez-Rosado F, Alvarez-Cubero MJ, Martinez-Espin E, Entrala-Bernal C. Cabrera-Bueno F, et al. Among authors: entrala bernal c. J Cardiol Cases. 2014 Sep 26;10(6):235-237. doi: 10.1016/j.jccase.2014.08.007. eCollection 2014 Dec. J Cardiol Cases. 2014. PMID: 30534251 Free PMC article.
Response to an expanding role of biomarkers in acute aortic syndromes.
Cabrera-Bueno F, Alvarez-Cubero MJ, Fernandez-Rosado F, Martinez-Espin E, Entrala-Bernal C. Cabrera-Bueno F, et al. Among authors: entrala bernal c. Clin Cardiol. 2014 Sep;37(9):589. doi: 10.1002/clc.22317. Epub 2014 Jul 18. Clin Cardiol. 2014. PMID: 25041814 Free PMC article. No abstract available.
New genetic variants of genes MMR in a Spanish family with Lynch syndrome.
Martín Ruiz JL, Alvarez-Cubero MJ, Fernandez Rosado J, Martinez Espín E, Entrala Bernal C. Martín Ruiz JL, et al. Int J Colorectal Dis. 2013 Oct;28(10):1451-2. doi: 10.1007/s00384-012-1615-3. Epub 2012 Dec 8. Int J Colorectal Dis. 2013. PMID: 23224667 No abstract available.
Novel FA2H mutation in a girl with familial spastic paraplegia.
Aguirre-Rodríguez FJ, Lucenilla MI, Alvarez-Cubero MJ, Mata C, Entrala-Bernal C, Fernandez-Rosado F. Aguirre-Rodríguez FJ, et al. Among authors: entrala bernal c. J Neurol Sci. 2015 Oct 15;357(1-2):332-4. doi: 10.1016/j.jns.2015.07.042. Epub 2015 Aug 29. J Neurol Sci. 2015. PMID: 26344562 No abstract available.
A comprehensive study of circulating tumour cells at the moment of prostate cancer diagnosis: biological and clinical implications of EGFR, AR and SNPs.
Puche-Sanz I, Alvarez-Cubero MJ, Pascual-Geler M, Rodríguez-Martínez A, Delgado-Rodríguez M, García-Puche JL, Expósito J, Robles-Fernández I, Entrala-Bernal C, Lorente JA, Cózar-Olmo JM, Serrano MJ. Puche-Sanz I, et al. Among authors: entrala bernal c. Oncotarget. 2017 Jul 31;8(41):70472-70480. doi: 10.18632/oncotarget.19718. eCollection 2017 Sep 19. Oncotarget. 2017. PMID: 29050295 Free PMC article.
Identification of SYNJ1 in a Complex Case of Juvenile Parkinsonism Using a Multiomics Approach.
Leno-Durán E, Arrabal L, Roldán S, Medina I, Alcántara-Domínguez C, García-Cabrera V, Saiz J, Barbas C, Sánchez MJ, Entrala-Bernal C, Fernández-Rosado F, Lorente JA, Gutierrez-Ríos P, Martínez-Gonzalez LJ. Leno-Durán E, et al. Among authors: entrala bernal c. Int J Mol Sci. 2024 Sep 9;25(17):9754. doi: 10.3390/ijms25179754. Int J Mol Sci. 2024. PMID: 39273702 Free PMC article.
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