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NewsMeSH: A new classifier designed to annotate health news with MeSH headings.
Artif Intell Med. 2021 Apr;114:102053. doi: 10.1016/j.artmed.2021.102053. Epub 2021 Mar 13.
Artif Intell Med. 2021.
PMID: 33875160
In search of an evidence-based strategy for quality assessment of human tissue samples: report of the tissue Biospecimen Research Working Group of the Spanish Biobank Network.
Esteva-Socias M, Artiga MJ, Bahamonde O, Belar O, Bermudo R, Castro E, Escámez T, Fraga M, Jauregui-Mosquera L, Novoa I, Peiró-Chova L, Rejón JD, Ruiz-Miró M, Vieiro-Balo P, Villar-Campo V, Zazo S, Rábano A, Villena C.
Esteva-Socias M, et al. Among authors: belar o.
J Transl Med. 2019 Nov 12;17(1):370. doi: 10.1186/s12967-019-2124-8.
J Transl Med. 2019.
PMID: 31718661
Free PMC article.
Review.
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Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain.
Belar O, De La Hoz C, Pérez-Nanclares G, Castaño L, Gaztambide S; Spanish MEN1 Group.
Belar O, et al.
Clin Endocrinol (Oxf). 2012 May;76(5):719-24. doi: 10.1111/j.1365-2265.2011.04269.x.
Clin Endocrinol (Oxf). 2012.
PMID: 22026581
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Clinical characterization of a girl with trisomy 20q13.2qter and monosomy 13q33.1qter: Delineating phenotype-genotype correlations.
Belar O, Del Pozo JS, Moreno-García M, Cruz-Rojo J, Garin I, de Nanclares GP.
Belar O, et al.
Am J Med Genet A. 2010 Nov;152A(11):2901-5. doi: 10.1002/ajmg.a.33679.
Am J Med Genet A. 2010.
PMID: 20949536
No abstract available.
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