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

Year Number of Results
1987 1
1989 1
1994 2
1996 2
1997 1
1998 1
1999 4
2000 2
2001 2
2003 2
2004 2
2005 3
2006 1
2007 1
2008 4
2009 5
2010 5
2011 6
2012 7
2013 4
2014 5
2015 3
2016 7
2017 12
2018 1
2019 9
2020 9
2021 9
2022 3
2023 1
2024 1

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105 results

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Page 1
Diagnosis of inborn errors of metabolism within the expanded newborn screening in the Madrid region.
Martín-Rivada Á, Palomino Pérez L, Ruiz-Sala P, Navarrete R, Cambra Conejero A, Quijada Fraile P, Moráis López A, Belanger-Quintana A, Martín-Hernández E, Bellusci M, Cañedo Villaroya E, Chumillas Calzada S, García Silva MT, Bergua Martínez A, Stanescu S, Martínez-Pardo Casanova M, Ruano MLF, Ugarte M, Pérez B, Pedrón-Giner C. Martín-Rivada Á, et al. Among authors: garcia silva mt. JIMD Rep. 2022 Jan 27;63(2):146-161. doi: 10.1002/jmd2.12265. eCollection 2022 Mar. JIMD Rep. 2022. PMID: 35281663 Free PMC article.
Understanding mitochondrial diseases.
García-Silva MT, Martín MA, Morán M. García-Silva MT, et al. Clin Nutr. 2017 Jun;36(3):902. doi: 10.1016/j.clnu.2017.03.013. Epub 2017 Mar 16. Clin Nutr. 2017. PMID: 28343800 No abstract available.
Recommendations for the Diagnosis and Therapeutic Management of Hyperammonaemia in Paediatric and Adult Patients.
Bélanger-Quintana A, Arrieta Blanco F, Barrio-Carreras D, Bergua Martínez A, Cañedo Villarroya E, García-Silva MT, Lama More R, Martín-Hernández E, López AM, Morales-Conejo M, Pedrón-Giner C, Quijada-Fraile P, Stanescu S, Casanova MM. Bélanger-Quintana A, et al. Among authors: garcia silva mt. Nutrients. 2022 Jul 2;14(13):2755. doi: 10.3390/nu14132755. Nutrients. 2022. PMID: 35807935 Free PMC article. Review.
Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-Hünermann-Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature.
Cañueto J, Girós M, Ciria S, Pi-Castán G, Artigas M, García-Dorado J, García-Patos V, Virós A, Vendrell T, Torrelo A, Hernández-Martín A, Martín-Hernández E, Garcia-Silva MT, Fernández-Burriel M, Rosell J, Tejedor M, Martínez F, Valero J, García JL, Sánchez-Tapia EM, Unamuno P, González-Sarmiento R. Cañueto J, et al. Among authors: garcia silva mt. Br J Dermatol. 2012 Apr;166(4):830-8. doi: 10.1111/j.1365-2133.2011.10756.x. Epub 2012 Mar 2. Br J Dermatol. 2012. PMID: 22121851 Review.
[Transition process from paediatric to adult care in patients with inborn errors of metabolism. Consensus statement].
Pérez-López J, Ceberio-Hualde L, García Morillo JS, Grau-Junyent JM, Hermida Ameijeiras Á, López-Rodríguez M, Morales-Conejo M, Nava Mateos JJ, Aldámiz Echevarri Azuara LJ, Campistol J, Couce ML, García-Silva MT, González Gutiérrez-Solana L, Del Toro M; Sociedad Española de Medicina Interna (SEMI); Sociedad Española de Neurología Pediátrica (SENEP). Pérez-López J, et al. Among authors: garcia silva mt. Med Clin (Barc). 2016 Dec 2;147(11):506.e1-506.e7. doi: 10.1016/j.medcli.2016.09.018. Epub 2016 Nov 3. Med Clin (Barc). 2016. PMID: 27816186 Spanish.
Characterization of a heme-protein responsive to hypoxia in Paracoccidioides brasiliensis.
Nojosa Oliveira L, Aguiar Gonçales R, Garcia Silva M, Melo Lima R, Vieira Tomazett M, Santana de Curcio J, Domiraci Paccez J, Milhomem Cruz-Leite VR, Rodrigues F, de Sousa Lima P, Pereira M, de Almeida Soares CM. Nojosa Oliveira L, et al. Among authors: garcia silva m. Fungal Genet Biol. 2020 Nov;144:103446. doi: 10.1016/j.fgb.2020.103446. Epub 2020 Aug 19. Fungal Genet Biol. 2020. PMID: 32822859 Free article.
105 results