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

Year Number of Results
1952 1
1958 1
1964 2
1965 2
1967 1
1968 4
1969 1
1974 2
1983 1
1984 2
1988 2
1989 2
1990 1
1991 1
1995 1
1996 7
1997 3
1998 6
1999 9
2000 7
2001 9
2002 14
2003 17
2004 23
2005 18
2006 19
2007 17
2008 21
2009 17
2010 21
2011 28
2012 16
2013 15
2014 9
2015 14
2016 12
2017 18
2018 11
2019 24
2020 31
2021 25
2022 28
2023 24
2024 11

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442 results

Results by year

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Page 1
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.
Picketts D, Mirzaa G, Yan K, Relator R, Timpano S, Yalcin B, Collins S, Ziegler A, Pao E, Oyama N, Brischoux-Boucher E, Piard J, Monaghan K, Sacoto MG, Dobyns W, Park K, Fernández-Mayoralas D, Fernández-Jaén A, Jayakar P, Brusco A, Antona V, Giorgio E, Kvarnung M, Isidor B, Conrad S, Cogné B, Deb W, Stuurman KE, Sterbova K, Smal N, Weckhuysen S, Oegema R, Innes M, Latsko M, Ben-Omran T, Yeh R, Kruer M, Bakhtiari S, Papavasiliou A, Moutton S, Nambot S, Chanprasert S, Paolucci S, Miller K, Burton B, Kim K, O'Heir E, Bruwer Z, Donald K, Kleefstra T, Goldstein A, Angle B, Bontempo K, Miny P, Joset P, Demurger F, Hobson E, Pang L, Carpenter L, Li D, Bonneau D, Sadikovic B. Picketts D, et al. Among authors: oyama n. Res Sq [Preprint]. 2023 Sep 29:rs.3.rs-3317938. doi: 10.21203/rs.3.rs-3317938/v1. Res Sq. 2023. PMID: 37841849 Free PMC article. Preprint.
Percutaneous pulmonary artery debanding.
Tomita H, Fujii T, Kise H, Oyama N, Shimizu T, Nagaoka K, Tarui S, Miyahara Y, Ishino K. Tomita H, et al. Among authors: oyama n. J Cardiol. 2021 Mar;77(3):307-312. doi: 10.1016/j.jjcc.2020.10.021. Epub 2020 Dec 2. J Cardiol. 2021. PMID: 33279375 Free article.
Behçet's disease (Adamantiades-Behçet's disease).
Kaneko F, Togashi A, Saito S, Sakuma H, Oyama N, Nakamura K, Yokota K, Oguma K. Kaneko F, et al. Among authors: oyama n. Clin Dev Immunol. 2011;2011:681956. doi: 10.1155/2011/681956. Epub 2010 Nov 1. Clin Dev Immunol. 2011. PMID: 21052488 Free PMC article. Review.
Variants in PTEN Are Associated With a Diverse Spectrum of Cortical Dysplasia.
Shelkowitz E, Stence NV, Neuberger I, Park KL, Saenz MS, Pao E, Oyama N, Friedman SD, Shaw DWW, Mirzaa GM. Shelkowitz E, et al. Among authors: oyama n. Pediatr Neurol. 2023 Oct;147:154-162. doi: 10.1016/j.pediatrneurol.2023.06.015. Epub 2023 Jun 22. Pediatr Neurol. 2023. PMID: 37619436
Psoriasis bullosa acquisita.
Morris SD, Mallipeddi R, Oyama N, Gratian MJ, Harman KE, Bhogal BS, Black MM, Eady RA, Hashimoto T, McGrath JA. Morris SD, et al. Among authors: oyama n. Clin Exp Dermatol. 2002 Nov;27(8):665-9. doi: 10.1046/j.1365-2230.2002.01100.x. Clin Exp Dermatol. 2002. PMID: 12472542
Mitochondrial haplotype mutation alleviates respiratory defect of MELAS by restoring taurine modification in tRNA with 3243A > G mutation.
Ueda S, Yagi M, Tomoda E, Matsumoto S, Ueyanagi Y, Do Y, Setoyama D, Matsushima Y, Nagao A, Suzuki T, Ide T, Mori Y, Oyama N, Kang D, Uchiumi T. Ueda S, et al. Among authors: oyama n. Nucleic Acids Res. 2023 Aug 11;51(14):7480-7495. doi: 10.1093/nar/gkad591. Nucleic Acids Res. 2023. PMID: 37439353 Free PMC article.
442 results