Nishikomori R - Search Results

1

The first case of adult-onset PFAPA syndrome in Japan.

Kutsuna S, Ohmagari N, Tanizaki R, Hagino N, Nishikomori R, Ujiie M, Takeshita N, Hayakawa K, Kato Y, Kanagawa S. Kutsuna S, et al. Among authors: nishikomori r. Mod Rheumatol. 2016;26(2):286-7. doi: 10.3109/14397595.2013.857801. Epub 2013 Dec 2. Mod Rheumatol. 2016. PMID: 24289199

2

Guidance on the use of canakinumab in patients with cryopyrin-associated periodic syndrome in Japan.

Yokota S, Nishikomori R, Takada H, Kikuchi M, Nozawa T, Kanetaka T, Kizawa T, Miyamae T, Mori M, Heike T, Hara T, Imagawa T. Yokota S, et al. Among authors: nishikomori r. Mod Rheumatol. 2013 May;23(3):425-9. doi: 10.1007/s10165-012-0769-8. Epub 2012 Oct 20. Mod Rheumatol. 2013. PMID: 23085882 Review.

3

MEFV Variants in Patients with PFAPA Syndrome in Japan.

Taniuchi S, Nishikomori R, Iharada A, Tuji S, Heike T, Kaneko K. Taniuchi S, et al. Among authors: nishikomori r. Open Rheumatol J. 2013 Apr 19;7:22-5. doi: 10.2174/1874312901307010022. Print 2013. Open Rheumatol J. 2013. PMID: 23847694 Free PMC article.

4

A 2-year-old Japanese girl with TNF receptor-associated periodic syndrome: A case report of the youngest diagnosed proband in Japan.

Yasumura J, Wago M, Okada S, Nishikomori R, Takei S, Kobayashi M. Yasumura J, et al. Among authors: nishikomori r. Mod Rheumatol. 2016 Sep;26(5):798-801. doi: 10.3109/14397595.2014.924894. Epub 2014 Jun 20. Mod Rheumatol. 2016. PMID: 24950168

5

CINCA syndrome with surgical intervention for valgus deformity and flexion contracture of the knee joint: A case report.

Harada Y, Fukiage K, Nishikomori R, Suzuki S, Futami T. Harada Y, et al. Among authors: nishikomori r. Mod Rheumatol. 2017 Nov;27(6):1098-1100. doi: 10.3109/14397595.2015.1040609. Epub 2015 Jun 13. Mod Rheumatol. 2017. PMID: 25867226

6

National survey of Japanese patients with mevalonate kinase deficiency reveals distinctive genetic and clinical characteristics.

Tanaka T, Yoshioka K, Nishikomori R, Sakai H, Abe J, Yamashita Y, Hiramoto R, Morimoto A, Ishii E, Arakawa H, Kaneko U, Ohshima Y, Okamoto N, Ohara O, Hata I, Shigematsu Y, Kawai T, Yasumi T, Heike T. Tanaka T, et al. Among authors: nishikomori r. Mod Rheumatol. 2019 Jan;29(1):181-187. doi: 10.1080/14397595.2018.1442639. Epub 2018 Mar 2. Mod Rheumatol. 2019. PMID: 29451047

7

Clinical phenotypes and genetic analyses for diagnosis of systemic autoinflammatory diseases in adult patients with unexplained fever.

Hidaka Y, Fujimoto K, Matsuo N, Koga T, Kaieda S, Yamasaki S, Nakashima M, Migita K, Nakayama M, Ohara O, Hoshino T, Nishikomori R, Ida H. Hidaka Y, et al. Among authors: nishikomori r. Mod Rheumatol. 2021 May;31(3):704-709. doi: 10.1080/14397595.2020.1784542. Epub 2020 Jul 24. Mod Rheumatol. 2021. PMID: 32552384

8

MEFV E148Q variant is more associated with familial Mediterranean fever when combined with other non-exon 10 MEFV variants in Japanese patients with recurrent fever.

Fujimoto K, Hidaka Y, Koga T, Kaieda S, Yamasaki S, Nakashima M, Hoshino T, Yamamoto K, Nishikomori R, Ida H. Fujimoto K, et al. Among authors: nishikomori r. Mod Rheumatol. 2021 Nov;31(6):1208-1214. doi: 10.1080/14397595.2021.1880534. Epub 2021 Mar 16. Mod Rheumatol. 2021. PMID: 33497256

9

Familial cases of periodic fever with aphthous stomatitis, pharyngitis, and cervical adenitis syndrome.

Adachi M, Watanabe A, Nishiyama A, Oyazato Y, Kamioka I, Murase M, Ishida A, Sakai H, Nishikomori R, Heike T. Adachi M, et al. Among authors: nishikomori r. J Pediatr. 2011 Jan;158(1):155-9. doi: 10.1016/j.jpeds.2010.09.054. Epub 2010 Nov 11. J Pediatr. 2011. PMID: 21074183

10

Patient with neonatal-onset chronic hepatitis presenting with mevalonate kinase deficiency with a novel MVK gene mutation.

Tahara M, Sakai H, Nishikomori R, Yasumi T, Heike T, Nagata I, Inui A, Fujisawa T, Shigematsu Y, Nishijima K, Kuwakado K, Watabe S, Kameyama J. Tahara M, et al. Among authors: nishikomori r. Mod Rheumatol. 2011 Dec;21(6):641-5. doi: 10.1007/s10165-011-0442-7. Epub 2011 Mar 12. Mod Rheumatol. 2011. PMID: 21399979

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