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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1994 1
1995 2
2006 2
2007 1
2008 1
2009 1
2010 3
2011 5
2012 5
2013 5
2014 1
2015 2
2016 2
2017 3
2018 2
2019 4
2020 1
2021 3
2022 2
2023 1
2024 0

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38 results

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Page 1
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
Garcia-Pelaez J, Barbosa-Matos R, Lobo S, Dias A, Garrido L, Castedo S, Sousa S, Pinheiro H, Sousa L, Monteiro R, Maqueda JJ, Fernandes S, Carneiro F, Pinto N, Lemos C, Pinto C, Teixeira MR, Aretz S, Bajalica-Lagercrantz S, Balmaña J, Blatnik A, Benusiglio PR, Blanluet M, Bours V, Brems H, Brunet J, Calistri D, Capellá G, Carrera S, Colas C, Dahan K, de Putter R, Desseignés C, Domínguez-Garrido E, Egas C, Evans DG, Feret D, Fewings E, Fitzgerald RC, Coulet F, Garcia-Barcina M, Genuardi M, Golmard L, Hackmann K, Hanson H, Holinski-Feder E, Hüneburg R, Krajc M, Lagerstedt-Robinson K, Lázaro C, Ligtenberg MJL, Martínez-Bouzas C, Merino S, Michils G, Novaković S, Patiño-García A, Ranzani GN, Schröck E, Silva I, Silveira C, Soto JL, Spier I, Steinke-Lange V, Tedaldi G, Tejada MI, Woodward ER, Tischkowitz M, Hoogerbrugge N, Oliveira C. Garcia-Pelaez J, et al. Among authors: garcia barcina m. Lancet Oncol. 2023 Jan;24(1):91-106. doi: 10.1016/S1470-2045(22)00643-X. Epub 2022 Nov 24. Lancet Oncol. 2023. PMID: 36436516 Free PMC article.
Brachydactyly E: isolated or as a feature of a syndrome.
Pereda A, Garin I, Garcia-Barcina M, Gener B, Beristain E, Ibañez AM, Perez de Nanclares G. Pereda A, et al. Among authors: garcia barcina m. Orphanet J Rare Dis. 2013 Sep 12;8:141. doi: 10.1186/1750-1172-8-141. Orphanet J Rare Dis. 2013. PMID: 24028571 Free PMC article. Review.
Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications.
Perea-Romero I, Gordo G, Iancu IF, Del Pozo-Valero M, Almoguera B, Blanco-Kelly F, Carreño E, Jimenez-Rolando B, Lopez-Rodriguez R, Lorda-Sanchez I, Martin-Merida I, Pérez de Ayala L, Riveiro-Alvarez R, Rodriguez-Pinilla E, Tahsin-Swafiri S, Trujillo-Tiebas MJ; ESRETNET Study Group; ERDC Study Group; Associated Clinical Study Group; Garcia-Sandoval B, Minguez P, Avila-Fernandez A, Corton M, Ayuso C. Perea-Romero I, et al. Sci Rep. 2021 Jan 15;11(1):1526. doi: 10.1038/s41598-021-81093-y. Sci Rep. 2021. PMID: 33452396 Free PMC article.
[Generalized arterial calcification in childhood: A case report].
Arbide Del Río N, Solano Iturri JD, García Barcina M, Sarasola Díez E. Arbide Del Río N, et al. Among authors: garcia barcina m. Rev Esp Patol. 2020 Jul-Sep;53(3):193-196. doi: 10.1016/j.patol.2019.02.005. Epub 2019 Apr 8. Rev Esp Patol. 2020. PMID: 32650971 Review. Spanish.
Non-endocrine hyperaldosteronism. When hormones are supporting players.
Paja-Fano M, Gutiérrez-Macías A, García-Barcina MJ. Paja-Fano M, et al. Among authors: garcia barcina mj. Endocrinol Diabetes Nutr (Engl Ed). 2022 Nov;69(9):763-766. doi: 10.1016/j.endien.2021.09.004. Epub 2022 Nov 16. Endocrinol Diabetes Nutr (Engl Ed). 2022. PMID: 36402732 No abstract available.
[Hepatic adenomatosis].
Lorenzo Garrido H, Rotaetxe Vacas O, García Barcina MJ, Muñoz García G, Martín Bejarano E. Lorenzo Garrido H, et al. Among authors: garcia barcina mj. An Pediatr (Barc). 2008 May;68(5):526-7. doi: 10.1157/13120056. An Pediatr (Barc). 2008. PMID: 18448003 Free article. Spanish. No abstract available.
Human liver-associated lymphocytes: an overview.
Winnock M, Garcia Barcina M, Lukomska B, Huet S, Saric J, Balabaud C, Bioulac-Sage P. Winnock M, et al. Among authors: garcia barcina m. J Gastroenterol Hepatol. 1995;10 Suppl 1:S43-6. doi: 10.1111/j.1440-1746.1995.tb01796.x. J Gastroenterol Hepatol. 1995. PMID: 8589341 Review.
Does arterial hypertension influence the onset of Huntington's disease?
Valcárcel-Ocete L, Fullaondo A, Alkorta-Aranburu G, García-Barcina M, Roos RAC, Hjermind LE, Saft C, Frontali M, Reilmann R, Rickards H; REGISTRY investigators of the European Huntington’s Disease Network (EHDN); Zubiaga AM, Aguirre A. Valcárcel-Ocete L, et al. Among authors: garcia barcina m. PLoS One. 2018 May 23;13(5):e0197975. doi: 10.1371/journal.pone.0197975. eCollection 2018. PLoS One. 2018. PMID: 29791508 Free PMC article.
Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion".
De la Casa-Fages B, Fernández-Eulate G, Gamez J, Barahona-Hernando R, Morís G, García-Barcina M, Infante J, Zulaica M, Fernández-Pelayo U, Muñoz-Oreja M, Urtasun M, Olaskoaga A, Zelaya V, Jericó I, Saez-Villaverde R, Catalina I, Sola E, Martínez-Sáez E, Pujol A, Ruiz M, Schlüter A, Spinazzola A, Muñoz-Blanco JL, Grandas F, Holt I, Álvarez V, López de Munaín A. De la Casa-Fages B, et al. Among authors: garcia barcina m. Mov Disord. 2019 Dec;34(12):1932-1933. doi: 10.1002/mds.27899. Mov Disord. 2019. PMID: 31845766 No abstract available.
Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism.
De la Casa-Fages B, Fernández-Eulate G, Gamez J, Barahona-Hernando R, Morís G, García-Barcina M, Infante J, Zulaica M, Fernández-Pelayo U, Muñoz-Oreja M, Urtasun M, Olaskoaga A, Zelaya V, Jericó I, Saez-Villaverde R, Catalina I, Sola E, Martínez-Sáez E, Pujol A, Ruiz M, Schlüter A, Spinazzola A, Muñoz-Blanco JL, Grandas F, Holt I, Álvarez V, López de Munaín A. De la Casa-Fages B, et al. Among authors: garcia barcina m. Mov Disord. 2019 Oct;34(10):1547-1561. doi: 10.1002/mds.27812. Epub 2019 Aug 21. Mov Disord. 2019. PMID: 31433872
38 results