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

Year Number of Results
1974 1
1975 1
1977 1
1986 1
2007 2
2008 1
2011 5
2012 8
2013 4
2014 3
2015 5
2016 3
2017 3
2018 3
2019 8
2020 6
2021 4
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50 results
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Page 1
Metagenome-wide association study of gut microbiome revealed novel aetiology of rheumatoid arthritis in the Japanese population.
Kishikawa T, Maeda Y, Nii T, Motooka D, Matsumoto Y, Matsushita M, Matsuoka H, Yoshimura M, Kawada S, Teshigawara S, Oguro E, Okita Y, Kawamoto K, Higa S, Hirano T, Narazaki M, Ogata A, Saeki Y, Nakamura S, Inohara H, Kumanogoh A, Takeda K, Okada Y. Kishikawa T, et al. Among authors: teshigawara s. Ann Rheum Dis. 2020 Jan;79(1):103-111. doi: 10.1136/annrheumdis-2019-215743. Epub 2019 Nov 7. Ann Rheum Dis. 2020. PMID: 31699813 Free PMC article.
[Chemerin, RBP4 and vaspin].
Wada J, Teshigawara S, Nakatsuka A. Wada J, et al. Among authors: teshigawara s. Nihon Rinsho. 2011 Jan;69 Suppl 1:231-6. Nihon Rinsho. 2011. PMID: 21766603 Review. Japanese. No abstract available.
Lack of association between a disease-susceptible single-nucleotide polymorphism, rs2230926 of TNFAIP3, and tumour necrosis factor inhibitor therapeutic failure in Japanese patients with rheumatoid arthritis.
Matsuoka H, Kabata D, Taura A, Matsui T, Takahi K, Hirano F, Katayama M, Okamoto A, Suenaga Y, Suematsu E, Yoshizawa S, Ohmura K, Ito S, Takaoka H, Oguro E, Kuzuya K, Okita Y, Udagawa C, Yoshimura M, Teshigawara S, Harada Y, Isoda K, Yoshida Y, Ohshima S, Tohma S, Saeki Y. Matsuoka H, et al. Among authors: teshigawara s. Scand J Rheumatol. 2020 May;49(3):253-255. doi: 10.1080/03009742.2020.1716992. Scand J Rheumatol. 2020. PMID: 32406335 No abstract available.
Sporotrichal Tenosynovitis Diagnosed Helpfully by Musculoskeletal Ultrasonography.
Shimizu T, Akita S, Harada Y, Oguro E, Okita Y, Shigesaka M, Matsuoka H, Nii T, Teshigawara S, Kudo-Tanaka E, Tsuji S, Matsushita M, Ohshima S, Hoshida Y, Hashimoto J, Saeki Y. Shimizu T, et al. Among authors: teshigawara s. Intern Med. 2017;56(10):1243-1246. doi: 10.2169/internalmedicine.56.7912. Epub 2017 May 15. Intern Med. 2017. PMID: 28502945 Free PMC article.
[Hypolipidemia of renal diseases].
Teshigawara S, Wada J, Makino H. Teshigawara S, et al. Nihon Rinsho. 2007 Jul 28;65 Suppl 7:645-8. Nihon Rinsho. 2007. PMID: 17824103 Review. Japanese. No abstract available.
A novel homoplasmic mitochondrial DNA mutation (m.13376T>C, p.I347T) of MELAS presenting characteristic medial temporal lobe atrophy.
Sasaki R, Ohta Y, Hatanaka N, Tadokoro K, Nomura E, Shang J, Takemoto M, Hishikawa N, Yamashita T, Omote Y, Morimoto E, Teshigawara S, Wada J, Goto YI, Abe K. Sasaki R, et al. Among authors: teshigawara s. J Neurol Sci. 2020 Jan 15;408:116460. doi: 10.1016/j.jns.2019.116460. Epub 2019 Oct 25. J Neurol Sci. 2020. PMID: 31689606 No abstract available.
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