Hermansky–Pudlak syndrome pulmonary fibrosis: a rare inherited interstitial lung disease by Tadafumi Yokoyama, Bernadette R. Gochuico

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An atypical case of Kawasaki disease with severe pneumonia in a neonate by Yoshiki Kawamura, Hiroki Miura, Kazuyoshi Saito, Takayuki Kanno, Tadafumi Yokoyama, Yuta Aizawa, Tetsushi Yoshikawa

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Age-Dependent Defects of Regulatory B Cells in Wiskott-Aldrich Syndrome Gene Knockout Mice. by Tadafumi Yokoyama, Ayumi Yoshizaki, Karen L Simon, Martha R Kirby, Stacie M Anderson, Fabio Candotti

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Thrombotic thrombocytopenic purpura with juvenile systemic lupus erythematosus: successful treatment with caplacizumab and rituximab by Tadafumi Yokoyama, Takuya Mimura, Hiroki Tanaka, Ria Kasahara, Masaaki Usami, Yusuke Matsuda, Toshihiro Fujiki, Taizo Wada

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Case report: A family of atypical hemolytic uremic syndrome involving a CFH::CFHR1 fusion gene and CFHR3-1-4-2 gene duplication by Yuko Tasaki, Hiroshi Tsujimoto, Tadafumi Yokoyama, Naotoshi Sugimoto, Shinji Kitajima, Hiroshi Fujii, Yoshihiko Hidaka, Noritoshi Kato, Shoichi Maruyama, Norimitsu Inoue, Taizo Wada

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Serum insulin-like growth factor-binding protein 2 levels as an indicator for disease severity in enterohemorrhagic Escherichia coli induced hemolytic uremic syndrome by Yuko Tasaki, Natsumi Inoue, Masaki Shimizu, Naotoshi Sugimoto, Sayaka Ishikawa, Mao Mizuta, Tadafumi Yokoyama, Mondo Kuroda, Kazuhide Ohta, Akihiro Yachie, Taizo Wada

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Cellular and molecular defects in a patient with Hermansky-Pudlak syndrome type 5. by Joshi Stephen, Tadafumi Yokoyama, Nathanial J Tolman, Kevin J O'Brien, Elena-Raluca Nicoli, Brian P Brooks, Laryssa Huryn, Steven A Titus, David R Adams, Dong Chen, William A Gahl, Bernadette R Gochuico, May Christine V Malicdan

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ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13. by Yihan Zhang, Haigen Huang, Gexin Zhao, Tadafumi Yokoyama, Hugo Vega, Yan Huang, Raman Sood, Kevin Bishop, Valerie Maduro, John Accardi, Camilo Toro, Cornelius F Boerkoel, Karen Lyons, William A Gahl, Xiaohong Duan, May Christine V Malicdan, Shuo Lin

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Correction: ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13. by Yihan Zhang, Haigen Huang, Gexin Zhao, Tadafumi Yokoyama, Hugo Vega, Yan Huang, Raman Sood, Kevin Bishop, Valerie Maduro, John Accardi, Camilo Toro, Cornelius F Boerkoel, Karen Lyons, William A Gahl, Xiaohong Duan, May Christine V Malicdan, Shuo Lin

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Progressive pulmonary fibrosis in a murine model of Hermansky-Pudlak syndrome by Shachar Abudi-Sinreich, Steven P. Bodine, Tadafumi Yokoyama, Nathanial J. Tolman, Michal Tyrlik, Lauren C. Testa, Chen G. Han, Heidi M. Dorward, Stephen M. Wincovitch, Yair Anikster, William A. Gahl, Resat Cinar, Bernadette R. Gochuico, May Christine V. Malicdan

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CB1R and iNOS are distinct players promoting pulmonary fibrosis in Hermansky–Pudlak syndrome by Resat Cinar, Joshua K. Park, Charles N. Zawatsky, Nathan J. Coffey, Steven P. Bodine, Jasmina Abdalla, Tadafumi Yokoyama, Tony Jourdan, Lindsey Jay, Mei Xing G. Zuo, Kevin J. O'Brien, Junfeng Huang, Ken Mackie, Asaf Alimardanov, Malliga R. Iyer, William A. Gahl, George Kunos, Bernadette R. Gochuico, May Christine V. Malicdan

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