Zobrazeno 1 - 10 of 13 pro vyhledávání: '"Yuno Korenaga"'
1
Akademický článek
Childhood primary angiitis of the central nervous system following COVID-19 vaccination (BNT162b2/Pfizer-BioNtech): A case report
Autor: Toshiki Ariyoshi, Madoka Hoshide, Takahiro Motonaga, Yuno Korenaga, Yoshihiro Azuma, Takuya Ichimura, Takeshi Matsushige, Shunji Hasegawa
Publikováno v: Human Vaccines & Immunotherapeutics, Vol 19, Iss 2 (2023)
Childhood primary angiitis of the central nervous system (cPACNS) is a vasculitis of unknown etiology that is confined to the central nervous system (CNS) and can lead to repeated cerebral infarctions if left untreated. Several cases of cPACNS after
Externí odkaz: https://doaj.org/article/19863380557c4f5a9b17723d016a16da
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2
Akademický článek
A novel mutation in early‐onset sarcoidosis/Blau syndrome: an association with Propionibacterium acnes
Autor: Fumiko Okazaki, Hiroyuki Wakiguchi, Yuno Korenaga, Tamaki Nakamura, Hiroki Yasudo, Shohei Uchi, Ryoji Yanai, Nobuyuki Asano, Yoshinobu Hoshii, Tsuyoshi Tanabe, Kazushi Izawa, Yoshitaka Honda, Ryuta Nishikomori, Keisuke Uchida, Yoshinobu Eishi, Shouichi Ohga, Shunji Hasegawa
Publikováno v: Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-8 (2021)
Abstract Background Early-onset sarcoidosis (EOS) and Blau syndrome (BS) are systemic inflammatory granulomatous diseases without visible pulmonary involvement, and are distinguishable from their sporadic and familial forms. The diseases are characte
Externí odkaz: https://doaj.org/article/54f6b49dc8c249f29511c3e28e50503d
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5
A novel mutation in early‐onset sarcoidosis/Blau syndrome: an association with Propionibacterium acnes
Autor: Ryuta Nishikomori, Yoshinobu Hoshii, Yoshitaka Honda, Yoshinobu Eishi, Shunji Hasegawa, Nobuyuki Asano, Yuno Korenaga, Shouichi Ohga, Keisuke Uchida, Fumiko Okazaki, Kazushi Izawa, Tsuyoshi Tanabe, Sho-Hei Uchi, Tamaki Nakamura, Hiroyuki Wakiguchi, Hiroki Yasudo, Ryoji Yanai
Publikováno v: Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-8 (2021)
Pediatric Rheumatology Online Journal
BackgroundEarly-onset sarcoidosis (EOS) and Blau syndrome (BS) are systemic inflammatory granulomatous diseases without visible pulmonary involvement, and are distinguishable from their sporadic and familial forms. The diseases are characterized by a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98417580e20428f6fd275f00bcaedc51
https://doi.org/10.1186/s12969-021-00505-5
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7
Serum cytokine profiles distinguish acute food protein-induced enterocolitis syndrome from mimicking diseases
Autor: Kenji Matsumoro, Shoichi Ohga, Fumiko Okazaki, Tamaki Nakamura, Seigo Korematsu, Yuno Korenaga, Seigo Okada, Ken Fukuda, Shunji Hasegawa, Hiroki Yasudo, Hiroyuki Wakiguchi
Background: Food protein-induced enterocolitis syndrome (FPIES) is a non-IgE cell-mediated food allergy characterized by repetitive vomiting and other gastrointestinal symptoms. Although little is known about FPIES pathophysiology, some cytokines hav
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1b4b35f3ed93f2a31c8e1b2508d82601
https://doi.org/10.22541/au.160097926.65189278
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8
Food Protein-Induced Enterocolitis Syndrome in Children with Down Syndrome: A Pilot Case-Control Study
Autor: Fumiko Okazaki, Hiroyuki Wakiguchi, Yuno Korenaga, Kazumasa Takahashi, Hiroki Yasudo, Ken Fukuda, Mototsugu Shimokawa, Shunji Hasegawa
Publikováno v: Nutrients, Vol 14, Iss 388, p 388 (2022)
Nutrients; Volume 14; Issue 2; Pages: 388
Nutrients
Food protein-induced enterocolitis syndrome (FPIES) is a non-immunoglobin E-mediated food hypersensitivity disorder. However, little is known about the clinical features of FPIES in patients with Down syndrome (DS). Medical records of children with D
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afc0e734d20e606dad4920638ec73ed3
https://doi.org/10.3390/nu14020388
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9
Adjunct cyclosporine therapy for refractory Kawasaki disease in a very young infant
Autor: Shouichi Ohga, Hiroko Yamada, Yuno Korenaga, Hideaki Akase, Yoshihiro Azuma, Seigo Okada, Yasuo Suzuki, Midori Wakabayashi-Takahara, Shunji Hasegawa
Publikováno v: Pediatrics International. 58:295-298
Herein we describe the case of a 6-week-old boy who developed complete Kawasaki disease (KD). The cytokine profile and activation of monocytes and subsequent T cells matched the typical feature of refractory KD. The patient received a total of three
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d2e14080ff32c262c23174d0df92b5a3
https://doi.org/10.1111/ped.12778
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