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

Year Number of Results
2002 9
2003 13
2004 6
2005 8
2006 11
2007 9
2008 9
2009 10
2010 21
2011 18
2012 9
2013 17
2014 23
2015 30
2016 18
2017 26
2018 24
2019 26
2020 44
2021 73
2022 49
2023 60
2024 24

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474 results

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Page 1
Allelic heterogeneity and abnormal vesicle recycling in PLAA-related neurodevelopmental disorders.
Iacomino M, Houerbi N, Fortuna S, Howe J, Li S, Scorrano G, Riva A, Cheng KW, Steiman M, Peltekova I, Yusuf A, Baldassari S, Tamburro S, Scudieri P, Musante I, Di Ludovico A, Guerrisi S, Balagura G, Corsello A, Efthymiou S, Murphy D, Uva P, Verrotti A, Fiorillo C, Delvecchio M, Accogli A, Elsabbagh M, Houlden H, Scherer SW, Striano P, Zara F, Chou TF, Salpietro V. Iacomino M, et al. Among authors: murphy d. Front Mol Neurosci. 2024 Apr 8;17:1268013. doi: 10.3389/fnmol.2024.1268013. eCollection 2024. Front Mol Neurosci. 2024. PMID: 38650658 Free PMC article.
Identification and support of autistic individuals within the UK Criminal Justice System: a practical approach based upon professional consensus with input from lived experience.
Woodhouse E, Hollingdale J, Davies L, Al-Attar Z, Young S, Vinter LP, Agyemang K, Bartlett C, Berryessa C, Chaplin E, Deeley Q, Freckelton I, Gerry F, Gudjonsson G, Maras K, Mattison M, McCarthy J, Mills R, Misch P, Murphy D, Allely C. Woodhouse E, et al. Among authors: murphy d. BMC Med. 2024 Apr 12;22(1):157. doi: 10.1186/s12916-024-03320-3. BMC Med. 2024. PMID: 38609939 Free PMC article.
An 85-Year-Old Woman with Unexplained Hypoxia.
O'Brien H, Franciosi AN, Murphy DJ, Shand JA, McCarthy C. O'Brien H, et al. Among authors: murphy dj. Ann Am Thorac Soc. 2024 Apr;21(4):658-662. doi: 10.1513/AnnalsATS.202306-578CC. Ann Am Thorac Soc. 2024. PMID: 38557418 No abstract available.
Approach to Pulmonary Nodules in Connective Tissue Disease.
Gaffney B, Murphy DJ. Gaffney B, et al. Among authors: murphy dj. Semin Respir Crit Care Med. 2024 Mar 28. doi: 10.1055/s-0044-1782656. Online ahead of print. Semin Respir Crit Care Med. 2024. PMID: 38547916
Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications.
Chelban V, Aksnes H, Maroofian R, LaMonica LC, Seabra L, Siggervåg A, Devic P, Shamseldin HE, Vandrovcova J, Murphy D, Richard AC, Quenez O, Bonnevalle A, Zanetti MN, Kaiyrzhanov R, Salpietro V, Efthymiou S, Schottlaender LV, Morsy H, Scardamaglia A, Tariq A, Pagnamenta AT, Pennavaria A, Krogstad LS, Bekkelund ÅK, Caiella A, Glomnes N, Brønstad KM, Tury S, Moreno De Luca A, Boland-Auge A, Olaso R, Deleuze JF, Anheim M, Cretin B, Vona B, Alajlan F, Abdulwahab F, Battini JL, İpek R, Bauer P, Zifarelli G, Gungor S, Kurul SH, Lochmuller H, Da'as SI, Fakhro KA, Gómez-Pascual A, Botía JA, Wood NW, Horvath R, Ernst AM, Rothman JE, McEntagart M, Crow YJ, Alkuraya FS, Nicolas G; SYNaPS Study Group; Arnesen T, Houlden H. Chelban V, et al. Among authors: murphy d. Nat Commun. 2024 Mar 13;15(1):2269. doi: 10.1038/s41467-024-46354-0. Nat Commun. 2024. PMID: 38480682 Free PMC article.
474 results