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

Year Number of Results
2005 1
2006 1
2007 1
2008 1
2010 1
2011 2
2013 3
2014 2
2015 2
2017 1
2018 3
2019 2
2020 6
2021 5
2022 5
2023 1
2024 2

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33 results

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Page 1
Sudden cardiac death triggered by minimal alcohol consumption in the context of novel PPA2 mutations in 2 unrelated families.
Gómez González C, Del Campo Cano I, Isabel Fernández-Avila A, Paz Suárez-Mier M, José Sagastizábal M, Álvarez García-Rovés R, Méndez Fernández I, Vilches S, Centeno Jiménez M, Siles Sánchez-Manjavacas A, Usano Carrasco A, Gonzalez-Vioque E, Pablo Ochoa J, Medrano C, González López E, García-Pavía P, Bermejo J, Angeles Espinosa Castro M. Gómez González C, et al. Among authors: gonzalez vioque e. Gene. 2024 Apr 4;916:148437. doi: 10.1016/j.gene.2024.148437. Online ahead of print. Gene. 2024. PMID: 38582264 Free article.
Editorial: NGS technologies of rare diseases diagnosis.
Couce ML, González-Vioque E. Couce ML, et al. Among authors: gonzalez vioque e. Front Pediatr. 2022 Nov 12;10:1032359. doi: 10.3389/fped.2022.1032359. eCollection 2022. Front Pediatr. 2022. PMID: 36444169 Free PMC article. No abstract available.
Frequency of hereditary transthyretin amyloidosis among elderly patients with transthyretin cardiomyopathy.
Maestro-Benedicto A, Vela P, de Frutos F, Mora N, Pomares A, Gonzalez-Vioque E, Briceño A, Cabrera E, Cobo-Marcos M, Dominguez F, Gonzalez-Lopez E, Segovia J, Lara-Pezzi E, Garcia-Pavia P. Maestro-Benedicto A, et al. Among authors: gonzalez vioque e. Eur J Heart Fail. 2022 Dec;24(12):2367-2373. doi: 10.1002/ejhf.2658. Epub 2022 Sep 11. Eur J Heart Fail. 2022. PMID: 35999650 Free PMC article.
Rapid Molecular Diagnosis of Genetically Inherited Neuromuscular Disorders Using Next-Generation Sequencing Technologies.
Barbosa-Gouveia S, Vázquez-Mosquera ME, González-Vioque E, Hermida-Ameijeiras Á, Sánchez-Pintos P, de Castro MJ, León SR, Gil-Fournier B, Domínguez-González C, Camacho Salas A, Negrão L, Fineza I, Laranjeira F, Couce ML. Barbosa-Gouveia S, et al. Among authors: gonzalez vioque e. J Clin Med. 2022 May 12;11(10):2750. doi: 10.3390/jcm11102750. J Clin Med. 2022. PMID: 35628876 Free PMC article.
Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis.
Vázquez-Mosquera ME, González-Vioque E, Barbosa-Gouveia S, Bellido-Guerrero D, Tejera-Pérez C, Martinez-Olmos MA, Fernández-Pombo A, Castaño-González LA, Chans-Gerpe R, Couce ML. Vázquez-Mosquera ME, et al. Among authors: gonzalez vioque e. Orphanet J Rare Dis. 2022 Mar 4;17(1):105. doi: 10.1186/s13023-022-02263-3. Orphanet J Rare Dis. 2022. PMID: 35246208 Free PMC article.
Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal Sengers Syndrome.
Barbosa-Gouveia S, Vázquez-Mosquera ME, Gonzalez-Vioque E, Hermida-Ameijeiras Á, Valverde LL, Armstrong-Moron J, Fons-Estupiña MDC, Wintjes LT, Kappen A, Rodenburg RJ, Couce ML. Barbosa-Gouveia S, et al. Among authors: gonzalez vioque e. Int J Mol Sci. 2021 Dec 15;22(24):13484. doi: 10.3390/ijms222413484. Int J Mol Sci. 2021. PMID: 34948281 Free PMC article.
The search for an autoimmune origin of psychotic disorders: Prevalence of autoantibodies against hippocampus antigens, glutamic acid decarboxylase and nuclear antigens.
Hoffmann C, Zong S, Mané-Damas M, Stevens J, Malyavantham K, Küçükali Cİ, Tüzün E, De Hert M, van Beveren NJM, González-Vioque E, Arango C, Damoiseaux JGMC, Rutten BP, Molenaar PC, Losen M, Martinez-Martinez P. Hoffmann C, et al. Among authors: gonzalez vioque e. Schizophr Res. 2021 Feb;228:462-471. doi: 10.1016/j.schres.2020.12.038. Epub 2021 Feb 11. Schizophr Res. 2021. PMID: 33581586 Free article.
33 results