日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Serum Cytokine Profiling Differentiates Underlying Diseases in Cytokine Storm Syndrome

血清细胞因子谱分析可鉴别细胞因子风暴综合征的潜在疾病

Kaneko, Shuya; Hatano, Maho; Shimbo, Asami; Miyaoka, Futaba; Irabu, Hitoshi; Akutsu, Yuko; Hayashi, Yuko; Mizuta, Mao; Nakagishi, Yasuo; Akamine, Keiji; Iwata, Naomi; Furuno, Kenji; Tanaka, Takayuki; Ueno, Kazuyuki; Fujita, Shuhei; Yokoyama, Koji; Minato, Toshinori; Izawa, Kazushi; Yasumi, Takahiro; Matsubayashi, Tadashi; Hosoya, Tadashi; Nishikawa, Hiroki; Fujimura, Junya; Asano, Ryoko; Sugita, Yuko; Watanabe, Kenichi; Kobayashi, Anna; Endo, Takuya; Eguchi, Katsuhide; Nishikomori, Ryuta; Yasuoka, Ryuhei; Asano, Takaki; Kanno, Miyako; Hamada, Kazuya; Fujita, Yuji; Hayashi, Daisuke; Watanabe, Shojiro; Shiba, Takeshi; Yasuda, Shinsuke; Mori, Masaaki; Kanegane, Hirokazu; Takagi, Masatoshi; Shimizu, Masaki

Correction to: An international survey of allogeneic hematopoietic cell transplantation for X-linked agammaglobulinemia

更正:一项关于X连锁无丙种球蛋白血症异基因造血干细胞移植的国际调查

Nishimura, Akira; Uppuluri, Ramya; Raj, Revathi; Swaminathan, Venkateswaran Vellaichamy; Cheng, Yifei; Abu-Arja, Rolla F; Fu, Bin; Laberko, Alexandra; Albert, Michael H; Hauck, Fabian; Bucciol, Giorgia; Bigley, Venetia; Elcombe, Suzanne; Kharya, Gaurav; Pronk, Cornelis Jan H; Wehr, Claudia; Neven, Bénédicte; Warnatz, Klaus; Meyts, Isabelle; Morio, Tomohiro; Gennery, Andrew R; Kanegane, Hirokazu

Two Cases of CLIPPERS-like Syndrome Sharing a Hypomorphic UNC13D Variant

两例类似 CLIPPERS 综合征的病例共享一个功能减弱的 UNC13D 变异

Sagawa, Hirotaka; Hirata, Kosei; Katayama, Saori; Shibata, Hirofumi; Toyofuku, Etsushi; Kaneko, Shuya; Katata, Yu; Takezawa, Yusuke; Uematsu, Mitsugu; Onishi, Iichiroh; Yamazaki, Yuto; Hattori, Takaaki; Yamamoto, Masahide; Shimizu, Masaki; Imai, Kohsuke; Yasumi, Takahiro; Morio, Tomohiro; Yokota, Takanori; Sasahara, Yoji; Kanegane, Hirokazu

Rapid flow cytometric diagnosis of XIAP deficiency

快速流式细胞术诊断XIAP缺乏症

Wakatsuki, Ryosuke; Nishimura, Madoka; Tomomasa, Dan; Takahashi, Shuhei; Suzuki, Kyogo; Kawaguchi, Koji; Saura, Ryutaro; Inoue, Shota; Takeuchi, Ichiro; Arai, Katsuhiro; Sugiyama, Masanaka; Narishige, Yuta; Oshima, Akira; Tsumura, Miyuki; Okada, Satoshi; Hoshino, Akihiro; Takagi, Masatoshi; Kanegane, Hirokazu

Safety and Pharmacokinetics of Nirsevimab in Japanese Infants: Primary Analysis of the Open-Label JUBILUS Trial

Nirsevimab在日本婴儿中的安全性和药代动力学:开放标签JUBILUS试验的主要分析

Mori, Masaaki; Leach, Susannah; Learoyd, Maria; Vijapur, Divya; Sadow, Sam; Wilkins, Deidre; Abe, Yoshifusa; Ikeda, Kazushige; Kanegane, Hirokazu; Kano, Zempei; Moriuchi, Hiroyuki; Muneuchi, Jun; Nishikomori, Ryuta; Okazaki, Kaoru; Takas, Therese; Sakaguchi, Ayako; Villafana, Tonya

Classical Hodgkin lymphoma associated with immune deficiency and dysregulation exhibits a prognosis similar to sporadic cases but with distinct predictive markers

与免疫缺陷和失调相关的经典型霍奇金淋巴瘤的预后与散发性病例相似,但具有不同的预测标志物。

Mukae, Junichi; Akiyama, Hiroki; Tanaka, Keisuke; Yoshifuji, Kota; Nogami, Ayako; Umezawa, Natsuka; Umezawa, Yoshihiro; Yamamoto, Kouhei; Nagao, Toshikage; Yasuda, Shinsuke; Kanegane, Hirokazu; Takagi, Masatoshi; Mori, Takehiko; Yamamoto, Masahide

Papulonecrotic tuberculid in an infant

婴儿丘疹坏死性结核疹

Fukada, Hanaka; Hoshino, Akihiro; Kunieda, Junko; Takeshita, Hana; Kanegane, Hirokazu

Monoallelic mutations in MMD2 cause autosomal dominant aggressive periodontitis.

MMD2基因的单等位基因突变会导致常染色体显性遗传的侵袭性牙周炎

Iwata Tomoyuki, Mizoguchi Yoko, Yoshimoto Tetsuya, Tsumura Miyuki, Sakura Fumiaki, Johnson Jeffrey R, Matsuda Shinji, Ouhara Kazuhisa, Nagatani Yukiko, Asano Takaki, Ohnishi Hidenori, Kato Zenichiro, Mihara Keichiro, Kanegane Hirokazu, Ueda Tomoya, Sasaki Shinya, Taniguchi Yuri, Ninomiya Yurika, Ohno Yoshinori, Suzuki-Takedachi Kyoko, Sotomaru Yusuke, Sakuma Tetsushi, Yamamoto Takashi, Matsuda Yukiko, Kume Kodai, Sanui Terukazu, Nishimura Fusanori, Kajiya Mikihito, Ueki Yasuyoshi, Kurihara Hidemi, Morino Hiroyuki, Okada Satoshi, Kawakami Hideshi, Mizuno Noriyoshi

Editorial: Community series in primary immunodeficiencies worldwide, volume II

社论:全球原发性免疫缺陷社区系列,第二卷

Condino-Neto, Antonio; Korganow, Anne-Sophie; Kanegane, Hirokazu

Case Report: CD40LG Arg203Ile variant underlies atypical phenotype of X-linked hyper IgM syndrome

病例报告:CD40LG Arg203Ile变异是X连锁高IgM综合征非典型表型的致病因素

Nishikawa, Takuro; Tomomasa, Dan; Hijikata, Atsushi; Kasabata, Hiroshi; Okamoto, Yasuhiro; Ochs, Hans D; Kanegane, Hirokazu