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

Year Number of Results
1950 1
1974 1
1977 1
1981 1
1982 3
1983 1
1984 3
1985 3
1986 5
1987 3
1988 9
1989 4
1990 5
1991 4
1992 4
1993 4
1994 2
1995 5
1996 4
1997 6
1998 4
1999 3
2000 10
2001 6
2002 3
2003 4
2004 9
2005 6
2006 6
2007 11
2008 7
2009 8
2010 11
2011 23
2012 21
2013 32
2014 38
2015 38
2016 39
2017 34
2018 36
2019 25
2020 27
2021 33
2022 41
2023 40
2024 31

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513 results

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Page 1
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
Rivière JB, Mirzaa GM, O'Roak BJ, Beddaoui M, Alcantara D, Conway RL, St-Onge J, Schwartzentruber JA, Gripp KW, Nikkel SM, Worthylake T, Sullivan CT, Ward TR, Butler HE, Kramer NA, Albrecht B, Armour CM, Armstrong L, Caluseriu O, Cytrynbaum C, Drolet BA, Innes AM, Lauzon JL, Lin AE, Mancini GM, Meschino WS, Reggin JD, Saggar AK, Lerman-Sagie T, Uyanik G, Weksberg R, Zirn B, Beaulieu CL; Finding of Rare Disease Genes (FORGE) Canada Consortium; Majewski J, Bulman DE, O'Driscoll M, Shendure J, Graham JM Jr, Boycott KM, Dobyns WB. Rivière JB, et al. Among authors: armour cm. Nat Genet. 2012 Jun 24;44(8):934-40. doi: 10.1038/ng.2331. Nat Genet. 2012. PMID: 22729224 Free PMC article.
Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study.
Groeneweg S, van Geest FS, Abacı A, Alcantud A, Ambegaonkar GP, Armour CM, Bakhtiani P, Barca D, Bertini ES, van Beynum IM, Brunetti-Pierri N, Bugiani M, Cappa M, Cappuccio G, Castellotti B, Castiglioni C, Chatterjee K, de Coo IFM, Coutant R, Craiu D, Crock P, DeGoede C, Demir K, Dica A, Dimitri P, Dolcetta-Capuzzo A, Dremmen MHG, Dubey R, Enderli A, Fairchild J, Gallichan J, George B, Gevers EF, Hackenberg A, Halász Z, Heinrich B, Huynh T, Kłosowska A, van der Knaap MS, van der Knoop MM, Konrad D, Koolen DA, Krude H, Lawson-Yuen A, Lebl J, Linder-Lucht M, Lorea CF, Lourenço CM, Lunsing RJ, Lyons G, Malikova J, Mancilla EE, McGowan A, Mericq V, Lora FM, Moran C, Müller KE, Oliver-Petit I, Paone L, Paul PG, Polak M, Porta F, Poswar FO, Reinauer C, Rozenkova K, Menevse TS, Simm P, Simon A, Singh Y, Spada M, van der Spek J, Stals MAM, Stoupa A, Subramanian GM, Tonduti D, Turan S, den Uil CA, Vanderniet J, van der Walt A, Wémeau JL, Wierzba J, de Wit MY, Wolf NI, Wurm M, Zibordi F, Zung A, Zwaveling-Soonawala N, Visser WE. Groeneweg S, et al. Among authors: armour cm. Lancet Diabetes Endocrinol. 2020 Jul;8(7):594-605. doi: 10.1016/S2213-8587(20)30153-4. Lancet Diabetes Endocrinol. 2020. PMID: 32559475 Free PMC article.
No 348-Directive clinique de la SOGC et du CCGM : mise à jour sur le dépistage prénatal de l’aneuploïdie fœtale, des anomalies fœtales et des issues défavorables de la grossesse.
Audibert F, De Bie I, Johnson JA, Okun N, Wilson RD, Armour C, Chitayat D, Kim R. Audibert F, et al. Among authors: armour c. J Obstet Gynaecol Can. 2017 Sep;39(9):818-832. doi: 10.1016/j.jogc.2017.05.011. J Obstet Gynaecol Can. 2017. PMID: 28859767 French. No abstract available.
Burosumab for the treatment of cutaneous-skeletal hypophosphatemia syndrome.
Abebe L, Phung K, Robinson ME, Waldner R, Carsen S, Smit K, Tice A, Lazier J, Armour C, Page M, Dover S, Rauch F, Koujok K, Ward LM. Abebe L, et al. Among authors: armour c. Bone Rep. 2023 Nov 11;20:101725. doi: 10.1016/j.bonr.2023.101725. eCollection 2024 Mar. Bone Rep. 2023. PMID: 38229908 Free PMC article.
Trauma and trauma care in Europe.
Schäfer I, Hopchet M, Vandamme N, Ajdukovic D, El-Hage W, Egreteau L, Javakhishvili JD, Makhashvili N, Lampe A, Ardino V, Kazlauskas E, Mouthaan J, Sijbrandij M, Dragan M, Lis-Turlejska M, Figueiredo-Braga M, Sales L, Arnberg F, Nazarenko T, Nalyvaiko N, Armour C, Murphy D. Schäfer I, et al. Among authors: armour c. Eur J Psychotraumatol. 2018 Dec 20;9(1):1556553. doi: 10.1080/20008198.2018.1556553. eCollection 2018. Eur J Psychotraumatol. 2018. PMID: 30637092 Free PMC article. Review.
Alexa, write my exam: ChatGPT for MCQ creation.
Schneid SD, Armour C, Evans S, Brandl K. Schneid SD, et al. Among authors: armour c. Med Educ. 2024 Nov;58(11):1373-1374. doi: 10.1111/medu.15496. Epub 2024 Aug 30. Med Educ. 2024. PMID: 39212370 No abstract available.
Molecular characterization of 13 patients with PIK3CA-related overgrowth spectrum using a targeted deep sequencing approach.
de Kock L, Cuillerier A, Gillespie M, Couse M, Hartley T, Mears W, Bernier FP, Chudley AE, Frosk P, Nikkel SM, Innes AM, Lauzon J, Thomas M, Guerin A, Armour CM, Weksberg R, Scott JN, Watkins D, Harvey S, Cytrynbaum C; Care4Rare Canada Consortium; Kernohan KD, Boycott KM. de Kock L, et al. Among authors: armour cm. Am J Med Genet A. 2024 Mar;194(3):e63466. doi: 10.1002/ajmg.a.63466. Epub 2023 Nov 10. Am J Med Genet A. 2024. PMID: 37949664
Factors associated with anxiety disorder comorbidity.
Davies MR, Glen K, Mundy J, Ter Kuile AR, Adey BN, Armour C, Assary E, Coleman JRI, Goldsmith KA, Hirsch CR, Hotopf M, Hübel C, Jones IR, Kalsi G, Krebs G, McIntosh AM, Morneau-Vaillancourt G, Peel AJ, Purves KL, Lee SH, Skelton M, Smith DJ, Veale D, Walters JTR, Young KS, Zvrskovec J, Breen G, Eley TC. Davies MR, et al. Among authors: armour c. J Affect Disord. 2023 Feb 15;323:280-291. doi: 10.1016/j.jad.2022.11.051. Epub 2022 Nov 26. J Affect Disord. 2023. PMID: 36442657 Free PMC article.
513 results