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Development of hypertriglyceridemia due to GPIHBP1 autoantibodies prior to clinical diagnosis of systemic lupus erythematosus in a 14-year-old girl.
Allergol Int. 2022 Oct;71(4):555-557. doi: 10.1016/j.alit.2022.05.001. Epub 2022 Jun 2.
Allergol Int. 2022.
PMID: 35662538
Free article.
No abstract available.
Fasting-associated urticaria and/or anaphylaxis: A case report.
Kunitsu T, Ueba S, Nakajima R, Nonomura K, Maruo Y, Hide M.
Kunitsu T, et al.
Allergol Int. 2021 Apr;70(2):271-273. doi: 10.1016/j.alit.2020.09.006. Epub 2020 Nov 1.
Allergol Int. 2021.
PMID: 33139200
Free article.
No abstract available.
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Neonatal Meckel diverticulum: Obstruction due to a short mesodiverticular band.
Kunitsu T, Koshida S, Tanaka K, Nakahara S, Yanagi T, Maruo Y, Takeuchi Y, Kubota Y.
Kunitsu T, et al.
Pediatr Int. 2015 Oct;57(5):1007-9. doi: 10.1111/ped.12694. Epub 2015 Aug 26.
Pediatr Int. 2015.
PMID: 26310428
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Airway obstruction caused by rapid enlargement of cervical lymphangioma in a five-month-old boy.
Shimizu J, Taga T, Kishimoto T, Ohta M, Tagawa K, Kunitsu T, Yamane T, Tsujita Y, Kubota Y, Eguchi Y.
Shimizu J, et al. Among authors: kunitsu t.
Clin Case Rep. 2016 Aug 17;4(9):896-8. doi: 10.1002/ccr3.659. eCollection 2016 Sep.
Clin Case Rep. 2016.
PMID: 27648270
Free PMC article.
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Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency.
Tsujita Y, Mitsui-Sekinaka K, Imai K, Yeh TW, Mitsuiki N, Asano T, Ohnishi H, Kato Z, Sekinaka Y, Zaha K, Kato T, Okano T, Takashima T, Kobayashi K, Kimura M, Kunitsu T, Maruo Y, Kanegane H, Takagi M, Yoshida K, Okuno Y, Muramatsu H, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Kojima S, Ogawa S, Ohara O, Okada S, Kobayashi M, Morio T, Nonoyama S.
Tsujita Y, et al. Among authors: kunitsu t.
J Allergy Clin Immunol. 2016 Dec;138(6):1672-1680.e10. doi: 10.1016/j.jaci.2016.03.055. Epub 2016 Jul 14.
J Allergy Clin Immunol. 2016.
PMID: 27426521
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Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol-3-OH kinase δ syndrome type 1.
Okano T, Imai K, Tsujita Y, Mitsuiki N, Yoshida K, Kamae C, Honma K, Mitsui-Sekinaka K, Sekinaka Y, Kato T, Hanabusa K, Endo E, Takashima T, Hiroki H, Yeh TW, Tanaka K, Nagahori M, Tsuge I, Bando Y, Iwasaki F, Shikama Y, Inoue M, Kimoto T, Moriguchi N, Yuza Y, Kaneko T, Suzuki K, Matsubara T, Maruo Y, Kunitsu T, Waragai T, Sano H, Hashimoto Y, Tasaki K, Suzuki O, Shirakawa T, Kato M, Uchiyama T, Ishimura M, Tauchi T, Yagasaki H, Jou ST, Yu HH, Kanegane H, Kracker S, Durandy A, Kojima D, Muramatsu H, Wada T, Inoue Y, Takada H, Kojima S, Ogawa S, Ohara O, Nonoyama S, Morio T.
Okano T, et al. Among authors: kunitsu t.
J Allergy Clin Immunol. 2019 Jan;143(1):266-275. doi: 10.1016/j.jaci.2018.04.032. Epub 2018 May 18.
J Allergy Clin Immunol. 2019.
PMID: 29778502
Clinical Trial.
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A female patient with incomplete hemophagocytic lymphohistiocytosis caused by a heterozygous XIAP mutation associated with non-random X-chromosome inactivation skewed towards the wild-type XIAP allele.
Yang X, Hoshino A, Taga T, Kunitsu T, Ikeda Y, Yasumi T, Yoshida K, Wada T, Miyake K, Kubota T, Okuno Y, Muramatsu H, Adachi Y, Miyano S, Ogawa S, Kojima S, Kanegane H.
Yang X, et al. Among authors: kunitsu t.
J Clin Immunol. 2015 Apr;35(3):244-8. doi: 10.1007/s10875-015-0144-6. Epub 2015 Mar 7.
J Clin Immunol. 2015.
PMID: 25744037
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