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

Year Number of Results
1994 2
1995 2
1996 3
1997 2
1998 3
1999 2
2000 3
2001 7
2002 8
2003 10
2004 13
2005 20
2006 23
2007 31
2008 23
2009 24
2010 35
2011 36
2012 46
2013 50
2014 54
2015 59
2016 58
2017 85
2018 75
2019 72
2020 68
2021 65
2022 73
2023 55
2024 14

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848 results

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Page 1
Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome.
Boot E, Óskarsdóttir S, Loo JCY, Crowley TB, Orchanian-Cheff A, Andrade DM, Arganbright JM, Castelein RM, Cserti-Gazdewich C, de Reuver S, Fiksinski AM, Klingberg G, Lang AE, Mascarenhas MR, Moss EM, Nowakowska BA, Oechslin E, Palmer L, Repetto GM, Reyes NGD, Schneider M, Silversides C, Sullivan KE, Swillen A, van Amelsvoort TAMJ, Van Batavia JP, Vingerhoets C, McDonald-McGinn DM, Bassett AS. Boot E, et al. Genet Med. 2023 Mar;25(3):100344. doi: 10.1016/j.gim.2022.11.012. Epub 2023 Feb 2. Genet Med. 2023. PMID: 36729052 Free article.
Neuronal defects in a human cellular model of 22q11.2 deletion syndrome.
Khan TA, Revah O, Gordon A, Yoon SJ, Krawisz AK, Goold C, Sun Y, Kim CH, Tian Y, Li MY, Schaepe JM, Ikeda K, Amin ND, Sakai N, Yazawa M, Kushan L, Nishino S, Porteus MH, Rapoport JL, Bernstein JA, O'Hara R, Bearden CE, Hallmayer JF, Huguenard JR, Geschwind DH, Dolmetsch RE, Paşca SP. Khan TA, et al. Nat Med. 2020 Dec;26(12):1888-1898. doi: 10.1038/s41591-020-1043-9. Epub 2020 Sep 28. Nat Med. 2020. PMID: 32989314 Free PMC article.
Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Bassett AS, McDonald-McGinn DM, Devriendt K, Digilio MC, Goldenberg P, Habel A, Marino B, Oskarsdottir S, Philip N, Sullivan K, Swillen A, Vorstman J; International 22q11.2 Deletion Syndrome Consortium. Bassett AS, et al. J Pediatr. 2011 Aug;159(2):332-9.e1. doi: 10.1016/j.jpeds.2011.02.039. Epub 2011 May 12. J Pediatr. 2011. PMID: 21570089 Free PMC article. No abstract available.
Chromatin Modifications in 22q11.2 Deletion Syndrome.
Zhang Z, Shi L, Song L, Maurer K, Zhao X, Zackai EH, McGinn DE, Crowley TB, McGinn DMM, Sullivan KE. Zhang Z, et al. J Clin Immunol. 2021 Nov;41(8):1853-1864. doi: 10.1007/s10875-021-01123-2. Epub 2021 Aug 25. J Clin Immunol. 2021. PMID: 34435264
Otorhinologic Disorders in 22q11.2 Deletion Syndrome.
Lu N, Kacin AJ, Shaffer AD, Stapleton AL. Lu N, et al. Otolaryngol Head Neck Surg. 2023 Oct;169(4):1012-1019. doi: 10.1002/ohn.331. Epub 2023 Mar 23. Otolaryngol Head Neck Surg. 2023. PMID: 36950877
Tonsillectomy in Children with 22q11.2 Deletion Syndrome.
Arganbright JM, Hankey PB, Tracy M, Narayanan S, Noel-MacDonnell J, Ingram D. Arganbright JM, et al. Genes (Basel). 2022 Nov 23;13(12):2187. doi: 10.3390/genes13122187. Genes (Basel). 2022. PMID: 36553454 Free PMC article.
Heterotopia in Individuals with 22q11.2 Deletion Syndrome.
Neuhaus E, Hattingen E, Breuer S, Steidl E, Polomac N, Rosenow F, Rüber T, Herrmann E, Ecker C, Kushan L, Lin A, Vajdi A, Bearden CE, Jurcoane A. Neuhaus E, et al. AJNR Am J Neuroradiol. 2021 Nov;42(11):2070-2076. doi: 10.3174/ajnr.A7283. Epub 2021 Oct 7. AJNR Am J Neuroradiol. 2021. PMID: 34620586 Free PMC article.
Complement Activation in 22q11.2 Deletion Syndrome.
Grinde D, Øverland T, Lima K, Schjalm C, Mollnes TE, Abrahamsen TG. Grinde D, et al. J Clin Immunol. 2020 Apr;40(3):515-523. doi: 10.1007/s10875-020-00766-x. Epub 2020 Mar 9. J Clin Immunol. 2020. PMID: 32152940 Free PMC article.
848 results