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

Year Number of Results
2002 7
2003 2
2004 4
2005 4
2006 2
2007 5
2008 3
2009 5
2010 3
2011 3
2012 4
2013 6
2014 3
2015 10
2016 10
2017 3
2018 1
2019 8
2020 11
2021 6
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89 results
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Page 1
Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum.
Motta M, Pannone L, Pantaleoni F, Bocchinfuso G, Radio FC, Cecchetti S, Ciolfi A, Di Rocco M, Elting MW, Brilstra EH, Boni S, Mazzanti L, Tamburrino F, Walsh L, Payne K, Fernández-Jaén A, Ganapathi M, Chung WK, Grange DK, Dave-Wala A, Reshmi SC, Bartholomew DW, Mouhlas D, Carpentieri G, Bruselles A, Pizzi S, Bellacchio E, Piceci-Sparascio F, Lißewski C, Brinkmann J, Waclaw RR, Waisfisz Q, van Gassen K, Wentzensen IM, Morrow MM, Álvarez S, Martínez-García M, De Luca A, Memo L, Zampino G, Rossi C, Seri M, Gelb BD, Zenker M, Dallapiccola B, Stella L, Prada CE, Martinelli S, Flex E, Tartaglia M. Motta M, et al. Among authors: alvarez s. Am J Hum Genet. 2020 Sep 3;107(3):499-513. doi: 10.1016/j.ajhg.2020.06.018. Epub 2020 Jul 27. Am J Hum Genet. 2020. PMID: 32721402 Free PMC article.
ANO3 and early-onset dyskinetic encephalopathy.
Jiménez de Domingo A, Lopez-Martín S, Albert J, Jiménez de la Peña M, Tirado P, Fernández-Mayoralas DM, Fernández-Perrone AL, Calleja-Pérez B, Martínez-García M, Álvarez S, Fernández-Jaén A. Jiménez de Domingo A, et al. Among authors: alvarez s. Eur J Med Genet. 2020 Dec;63(12):104085. doi: 10.1016/j.ejmg.2020.104085. Epub 2020 Oct 9. Eur J Med Genet. 2020. PMID: 33045406
What Should Be Known by a Urologist About the Medical Management of COVID-19's Patients?
Sánchez-González Á, López-Fando Lavalle L, Esteban-Fernández A, Ruiz M, Hevia V, Comeche B, Sánchez Conde M, Álvarez S, Lorca Álvaro J, Fraile Poblador A, Hevia Palacios M, Domínguez Gutiérrez A, Artiles Medina A, Sanz Mayayo E, Duque G, Gómez Dos Santos V, Moreno-Guillén S, Burgos Revilla J. Sánchez-González Á, et al. Among authors: alvarez s. Curr Urol Rep. 2020 Sep 1;21(10):44. doi: 10.1007/s11934-020-00995-y. Curr Urol Rep. 2020. PMID: 32870407 Free PMC article. Review.
Distinct mutational pattern of myelodysplastic syndromes with and without 5q- treated with lenalidomide.
Adema V, Palomo L, Toma A, Kosmider O, Fuster-Tormo F, Benito R, Salgado R, Such E, Larrayoz MJ, Xicoy B, Hernandez-Sanchez JM, Maietta P, Neef A, Fontenay M, Ibañez M, Diez-Campelo M, Alvarez S, Maciejewski JP, Fenaux P, Sole F. Adema V, et al. Among authors: alvarez s. Br J Haematol. 2020 May;189(4):e133-e137. doi: 10.1111/bjh.16558. Epub 2020 Mar 9. Br J Haematol. 2020. PMID: 32147816 No abstract available.
Hereditary primary lateral sclerosis and progressive nonfluent aphasia.
Gazulla J, Ferrer I, Izquierdo-Alvarez S, Alvarez S, Sánchez-Alcudia R, Bestué-Cardiel M, Seral M, Benavente I, Sierra-Martínez E, Berciano J. Gazulla J, et al. Among authors: alvarez s. J Neurol. 2019 May;266(5):1079-1090. doi: 10.1007/s00415-019-09235-x. Epub 2019 Mar 5. J Neurol. 2019. PMID: 30834979 Free article.
Clinical manifestations of episodic ataxia type 5.
González Sánchez M, Izquierdo S, Álvarez S, Bautista Alonso RE, Berciano J, Gazulla J. González Sánchez M, et al. Among authors: alvarez s. Neurol Clin Pract. 2019 Dec;9(6):503-504. doi: 10.1212/CPJ.0000000000000697. Neurol Clin Pract. 2019. PMID: 32042491 Free PMC article. No abstract available.
A Novel Approach for the Identification of Pharmacogenetic Variants in MT-RNR1 through Next-Generation Sequencing Off-Target Data.
Lanillos J, Santos M, Carcajona M, Roldan-Romero JM, Martinez AM, Calsina B, Monteagudo M, Leandro-García LJ, Montero-Conde C, Cascón A, Maietta P, Alvarez S, Robledo M, Rodriguez-Antona C. Lanillos J, et al. Among authors: alvarez s. J Clin Med. 2020 Jul 2;9(7):2082. doi: 10.3390/jcm9072082. J Clin Med. 2020. PMID: 32630724 Free PMC article.
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