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

Year Number of Results
1951 1
1956 1
1958 1
1959 1
1961 1
1967 1
1968 1
1973 1
1974 1
1975 3
1977 1
1984 1
1989 1
1990 1
1992 1
1993 2
1994 2
1995 2
1996 2
1997 4
1998 6
1999 6
2000 5
2001 4
2002 4
2003 8
2004 7
2005 9
2006 7
2007 14
2008 7
2009 15
2010 6
2011 11
2012 8
2013 14
2014 21
2015 36
2016 24
2017 17
2018 22
2019 33
2020 23
2021 30
2022 17
2023 30
2024 14

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384 results

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Page 1
SARS-CoV-2 strains bearing Omicron BA.1 spike replicate in C57BL/6 mice.
Ogger PP, Martín MG, Jang S, Zhou J, Brown J, Sukhova K, Furnon W, Patel AH, Cowton V, Palmarini M, Barclay WS, Johansson C. Ogger PP, et al. Among authors: martin mg. Front Immunol. 2024 Apr 29;15:1383612. doi: 10.3389/fimmu.2024.1383612. eCollection 2024. Front Immunol. 2024. PMID: 38742107 Free PMC article.
Diet Management in Congenital Diarrheas and Enteropathies - General Concepts and Disease-Specific Approach, a Narrative Review.
Avitzur Y, Jimenez L, Martincevic I, Acra S, Courtney-Martin G, Gray M, Hope K, Muise A, Prieto Jimenez PM, Taylor N, Thiagarajah JR, Martín MG; PediCODE Consortium. Avitzur Y, et al. Among authors: martin mg. Am J Clin Nutr. 2024 May 9:S0002-9165(24)00466-0. doi: 10.1016/j.ajcnut.2024.05.004. Online ahead of print. Am J Clin Nutr. 2024. PMID: 38734141 Free article. Review.
De novo variants in DENND5B cause a neurodevelopmental disorder.
Scala M, Tomati V, Ferla M, Lena M, Cohen JS, Fatemi A, Brokamp E, Bican A, Phillips JA 3rd, Koziura ME, Nicouleau M, Rio M, Siquier K, Boddaert N, Musante I, Tamburro S, Baldassari S, Iacomino M, Scudieri P; Undiagnosed Diseases Network; Rosenfeld JA, Bellus G, Reed S, Al Saif H, Russo RS, Walsh MB, Cantagrel V, Crunk A, Gustincich S, Ruggiero SM, Fitzgerald MP, Helbig I, Striano P, Severino M, Salpietro V, Pedemonte N, Zara F. Scala M, et al. Am J Hum Genet. 2024 Mar 7;111(3):529-543. doi: 10.1016/j.ajhg.2024.02.001. Epub 2024 Feb 21. Am J Hum Genet. 2024. PMID: 38387458 Free PMC article.
MEFV gene mutation (c.229G>T) as a cause of fever of unknown origin.
Miramontes-González JP, Cristea AC, Martín MG, González Fernández M, Pérez-Castrillón JL. Miramontes-González JP, et al. Among authors: martin mg. Eur J Intern Med. 2024 May;123:151-152. doi: 10.1016/j.ejim.2024.01.026. Epub 2024 Feb 5. Eur J Intern Med. 2024. PMID: 38320885 No abstract available.
Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathy.
Donkervoort S, Mohassel P, O'Leary M, Bonner DE, Hartley T, Acquaye N, Brull A, Mozaffar T, Saporta MA, Dyment DA, Sampson JB, Pajusalu S, Austin-Tse C, Hurth K, Cohen JS, McWalter K, Warman-Chardon J, Crunk A, Foley AR; Undiagnosed Diseases Network; Mammen AL, Wheeler MT, O'Donnell-Luria A, Bönnemann CG. Donkervoort S, et al. Ann Clin Transl Neurol. 2024 Mar;11(3):629-640. doi: 10.1002/acn3.51983. Epub 2024 Feb 4. Ann Clin Transl Neurol. 2024. PMID: 38311799 Free PMC article.
384 results