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

Year Number of Results
1982 1
1983 1
1985 4
1986 2
1987 2
1988 4
1989 3
1990 4
1991 2
1992 4
1993 5
1994 3
1995 3
1996 2
1997 3
1998 3
1999 4
2000 5
2001 3
2002 2
2003 6
2004 5
2005 4
2006 5
2007 4
2008 8
2009 6
2010 4
2011 3
2012 8
2013 6
2014 4
2015 5
2016 9
2017 8
2018 9
2019 13
2020 11
2021 32
2022 24
2023 32
2024 19

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261 results

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Page 1
Comparative Effectiveness of a Second Tumor Necrosis Factor Inhibitor Versus a Non-Tumor Necrosis Factor Biologic in the Treatment of Patients With Polyarticular-Course Juvenile Idiopathic Arthritis.
Mannion ML, Amin S, Balevic S, Chang ML, Correll CK, Kearsley-Fleet L, Hyrich KL, Beukelman T; Childhood Arthritis and Rheumatology Research Alliance Registry Investigators and the UK Juvenile Idiopathic Arthritis Biologics Register Investigators. Mannion ML, et al. Arthritis Care Res (Hoboken). 2024 Mar 31. doi: 10.1002/acr.25339. Online ahead of print. Arthritis Care Res (Hoboken). 2024. PMID: 38556945
Enrichment of Rare Variants of Hemophagocytic Lymphohistiocytosis Genes in Systemic Juvenile Idiopathic Arthritis.
Marques MC, Rubin D, Shuldiner E, Datta M, Schmitz E, Cruz GG, Patt A, Bennett E, Grom A, Foell D, Gattorno M, Bohnsack J, Yeung RSM, Prahalad S, Mellins E, Anton J, Len CA, Oliveira S, Woo P, Ozen S; INCHARGE Consortium; Deng Z, Ombrello MJ. Marques MC, et al. Among authors: bohnsack j. medRxiv [Preprint]. 2024 Mar 15:2024.03.13.24304215. doi: 10.1101/2024.03.13.24304215. medRxiv. 2024. PMID: 38529491 Free PMC article. Preprint.
Correction to: Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers.
Patel PK, Chinga ML, Yilmaz M, Joychan S, Ujhazi B, Ellison M, Gordon S, Nieves D, Csomos K, Eslin D, Afify ZA, Meznarich J, Bohnsack J, Walkovich K, Seidel MG, Sharapova S, Boyarchuk O, Latysheva E, Tuzankina I, Shaker AB, Ayala I, Sriaroon P, Westermann-Clark E, Walter JE. Patel PK, et al. Among authors: bohnsack j. J Clin Immunol. 2024 Feb 29;44(3):72. doi: 10.1007/s10875-024-01677-x. J Clin Immunol. 2024. PMID: 38421526 No abstract available.
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.
261 results