Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Hidemasa Sakai"'
Autor:
Satoru Iwashima, Shinichiro Sano, Naoe Akiyama, Tetuya Fukuoka, Eiko Nagata, Masashi Harazaki, Hidemasa Sakai
Publikováno v:
Clinical drug investigation. 41(1)
Intravenous immunoglobulin (IVIG) therapy for acute-stage Kawasaki disease (KD) is the first-line treatment for preventing the development of coronary artery aneurysms (CAA). Corticosteroids (prednisolone) and infliximab are often used in patients at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d22c937479d00c812180ed70f4dc9cf
https://pubmed.ncbi.nlm.nih.gov/33341911
https://pubmed.ncbi.nlm.nih.gov/33341911
Autor:
Mitsuaki Kimura, Hidemasa Sakai, Isao Asakura, Ichiro Ohkawara, Tetsuya Fukuoka, Takaaki Meguro, Shiro Seto, Naoe Akiyama, Satoru Iwashima, Masaki Shimomura, Tsutomu Kamimaki, Masashi Harazaki, Satoshi Tsurui, Hideaki Morishita
Publikováno v:
Pediatrics International. 59:397-403
Background Prednisolone (PSL) has been suggested to be useful for the treatment of Kawasaki disease (KD) resistant to i.v. immunoglobulin (IVIG), but much remains to be elucidated regarding its use. Methods A total of 1087 subjects were involved in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fa1d4a1e537d6ef2fccad155f421375
https://doi.org/10.1111/ped.13190
https://doi.org/10.1111/ped.13190
Autor:
Tomoki Kawai, Toshio Heike, Nami Okamoto, Takayuki Tanaka, Yusei Ohshima, Ikue Hata, Junya Abe, Yuriko Yamashita, Ryugo Hiramoto, Osamu Ohara, Hidemasa Sakai, Utako Kaneko, Kohei Yoshioka, Akira Morimoto, Yosuke Shigematsu, Eiichi Ishii, Takahiro Yasumi, Ryuta Nishikomori, Hirokazu Arakawa
Publikováno v:
Modern rheumatology. 29(1)
Mevalonate kinase deficiency (MKD), a rare autosomal recessive autoinflammatory syndrome, is caused by disease-causing variants of the mevalonate kinase (MVK) gene. A national survey was undertaken to investigate clinical and genetic features of MKD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3f9c39f1043eae63696d34ba986fa95
https://pubmed.ncbi.nlm.nih.gov/29451047
https://pubmed.ncbi.nlm.nih.gov/29451047
Autor:
Satoshi Okada, Mohammed A. Al Shehri, Takuji Murata, Motoaki Ohtsubo, Miyuki Tsumura, Geyhad ElGhazali, Yoshihiro Takihara, Takahiro Yasumi, Ryuta Nishikomori, Masao Kobayashi, Jean-Laurent Casanova, Avinash Abhyankar, Shin'ichiro Yasunaga, Xiao-Fei Kong, Hideto Obata, Saleh Al-Muhsen, Tatsutoshi Nakahata, Toshio Heike, Mofareh AlZahrani, Hidemasa Sakai, Stéphanie Boisson-Dupuis
Publikováno v:
Human Mutation. 33:1377-1387
Patients carrying two loss-of-function (or hypomorphic) alleles of STAT1 are vulnerable to intracellular bacterial and viral diseases. Heterozygosity for loss-of-function dominant-negative mutations in STAT1 is responsible for autosomal dominant (AD)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::648003cf9953f9973fc66a7495e3894c
https://doi.org/10.1002/humu.22113
https://doi.org/10.1002/humu.22113
Autor:
Yuki Kiyohara, Tomoyuki Mizukami, Takahiro Yasumi, Etsuro Ito, Toshio Heike, Ryuta Nishikomori, Atsushi Yoden, Chihaya Imai, Tatsutoshi Nakahata, Satoshi Okada, Yuki Takaoka, Naoko Tanaka, Megumu K. Saito, Hiroshi Akutagawa, Yuuki Murata, Takuji Murata, Masao Kobayashi, Hiroyuki Nunoi, Tomoki Kawai, Shinya Sasaki, Toshinao Kawai, Kazushi Izawa, Hidemasa Sakai
Publikováno v:
Blood. 119:5458-5466
Somatic mosaicism has been described in several primary immunodeficiency diseases and causes modified phenotypes in affected patients. X-linked anhidrotic ectodermal dysplasia with immunodeficiency (XL-EDA-ID) is caused by hypomorphic mutations in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07a4489924d8099bec317e7a1c9da35c
https://doi.org/10.1182/blood-2011-05-354167
https://doi.org/10.1182/blood-2011-05-354167
Autor:
Hidemasa Sakai, Toshio Heike
Publikováno v:
Japanese Journal of Clinical Immunology. 34:382-387
Hyperimmunogloblinemia D and periodic fever syndrome (HIDS) is inherited autoinflammatory syndrome caused by deficiency of the mevalonate kinase (MK), which is involved in metabolism of cholesterol. The disease is characterized as periodic fever from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1686849a6497c304e819a3f25aa46fbf
https://doi.org/10.2177/jsci.34.382
https://doi.org/10.2177/jsci.34.382
Autor:
Hidemasa Sakai, Ichiro Kamioka, Atsushi Nishiyama, Masao Adachi, Aika Watanabe, Toshio Heike, Yoshinobu Oyazato, Masanori Murase, Akihito Ishida, Ryuta Nishikomori
Publikováno v:
The Journal of Pediatrics. 158:155-159
We report three familial cases of periodic fever with aphthous stomatitis, pharyngitis, and cervical adenitis syndrome, including a pair of monozygotic twins and their mother. It suggests that periodic fever with aphthous stomatitis, pharyngitis, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9323d9d769373c7d971b8c2edec67541
https://doi.org/10.1016/j.jpeds.2010.09.054
https://doi.org/10.1016/j.jpeds.2010.09.054
Autor:
Akihiro Fujisawa, Megumu K. Saito, Ryuta Nishikomori, Ikuo Okafuji, Shin Yamazaki, Tatsutoshi Nakahata, Nobuo Kanazawa, Toshio Heike, Naotomo Kambe, Hideaki Tanizaki, Yoshiki Miyachi, Hidemasa Sakai, Takakazu Yoshioka, Tomoki Kawai
Publikováno v:
Arthritis & Rheumatism. 60:242-250
Objective Blau syndrome and its sporadic counterpart, early-onset sarcoidosis (EOS), share a phenotype featuring the symptom triad of skin rash, arthritis, and uveitis. This systemic inflammatory granulomatosis is associated with mutations in the NOD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50c447e4437f7cea6406ce539979ba31
https://doi.org/10.1002/art.24134
https://doi.org/10.1002/art.24134
Autor:
Takayuki Tanaka, Kohei Yoshioka, Ryuta Nishikomori, Hidemasa Sakai, Junya Abe, Yuriko Yamashita, Ryugo Hiramoto, Akira Morimoto, Eiichi Ishii, Hirokazu Arakawa, Utako Kaneko, Yusei Ohshima, Nami Okamoto, Osamu Ohara, Ikue Hata, Yosuke Shigematsu, Tomoki Kawai, Takahiro Yasumi, Toshio Heike
Publikováno v:
Modern Rheumatology; 2019, Vol. 29 Issue 1, p181-187, 7p
Autor:
Tomoki Kawai, Ikuo Okafuji, Yuuki Takaoka, Tatsutoshi Nakahata, Megumu K. Saito, Hidemasa Sakai, Toshio Heike, Takahiro Yasumi, Ryuta Nishikomori, Shusaku Ito
Publikováno v:
Rheumatology. 49:194-196
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4b5b8f9e527901cc2406afcfcad13f0
https://doi.org/10.1093/rheumatology/kep315
https://doi.org/10.1093/rheumatology/kep315