Zobrazeno 1 - 10
of 209
pro vyhledávání: '"Autoimmune pulmonary alveolar proteinosis"'
Autor:
Ryushi Tazawa, Riuko Ohashi, Nobutaka Kitamura, Takahiro Tanaka, Kazuhide Nakagaki, Sachiko Yuki, Atsushi Fujiwara, Koh Nakata
Publikováno v:
Respiratory Research, Vol 25, Iss 1, Pp 1-16 (2024)
Abstract Background Repeated inhalation of granulocyte-macrophage colony-stimulating factor (GM-CSF) was recently approved in Japan as a treatment for autoimmune pulmonary alveolar proteinosis. However, the detailed physiological and pathological eff
Externí odkaz:
https://doaj.org/article/1a62f140078445beaa85530c0f805c98
Autor:
Masakiyo Yatomi, Keiichi Akasaka, Shintaro Sato, Mizuki Chida, Mio Kanbe, Hiru Sawada, Itaru Yokota, Ikuo Wakamatsu, Sohei Muto, Mari Sato, Kochi Yamaguchi, Yosuke Miura, Hiroaki Tsurumaki, Reiko Sakurai, Kenichiro Hara, Yasuhiko Koga, Noriaki Sunaga, Hideaki Yamakawa, Hidekazu Matsushima, Sahori Yamazaki, Yukie Endo, Sei-ichiro Motegi, Takeshi Hisada, Toshitaka Maeno
Publikováno v:
BMC Pulmonary Medicine, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background Autoimmune pulmonary alveolar proteinosis (APAP) is a diffuse lung disease that causes abnormal accumulation of lipoproteins in the alveoli; however, its pathogenesis remains unclear. Recently, APAP cases have been reported during
Externí odkaz:
https://doaj.org/article/25d54cd602984acd8d95a3cf2ecabe59
Autor:
Naoko Arakawa, Yuno Shiota, Fumi Onizawa, Fumi Miyata, Azusa Miyoshi, Tomohiro Akaba, Mayoko Tsuji, Ken Arimura, Osamitsu Yagi, Mitsuko Kondo, Hideki Katsura, Etsuko Tagaya
Publikováno v:
Respirology Case Reports, Vol 12, Iss 6, Pp n/a-n/a (2024)
Abstract A 46‐year‐old male was treated with corticosteroids for nonspecific interstitial pneumonia (NSIP). He was referred to our hospital and admitted for worsening dyspnea and diffuse ground‐glass opacity on chest computed tomography (CT) du
Externí odkaz:
https://doaj.org/article/fb7a3d654b0145849fb1cf777563714a
Autor:
Chuanxin Duan, Wangji Zhou, Miaoyan Zhang, Chongsheng Cheng, Wenshuai Xu, Jinrong Dai, Shuzhen Meng, Keqi Chen, Yang Zhao, Song Liu, Shao-Ting Wang, Yanli Yang, Kai-Feng Xu, Xinlun Tian
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Background Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare interstitial lung disease. COVID-19 is associated with worse prognosis in previous lung diseases patients. But the prognosis of aPAP patients after infection with COVID-19
Externí odkaz:
https://doaj.org/article/4f5aa18712f943bfa75523424edd226d
Akademický článek
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Autor:
Helena Lund-Palau, Claudia Ivette Juarez-Molina, Cuixiang Meng, Anushka Bhargava, Aikaterini Pilou, Kiran Aziz, Nora Clarke, Naoko Atsumi, Ali Ashek, Michael R. Wilson, Masao Takata, Simon Padley, Deborah R. Gill, Stephen C. Hyde, Cliff Morgan, Eric W.F.W. Alton, Uta Griesenbach
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 25, Iss , Pp 382-391 (2022)
We developed a novel lentiviral vector, pseudotyped with the F and HN proteins from Sendai virus (rSIV.F/HN), that produces long-lasting, high-efficiency transduction of the respiratory epithelium. Here we addressed whether this platform technology c
Externí odkaz:
https://doaj.org/article/4c2433997a7f402b8741006400d6273c
Publikováno v:
BMC Pulmonary Medicine, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Background Serum lactate dehydrogenase (LDH), carcinoembryonic antigen (CEA) and CYFRA21-1 are the commonly used biomarkers to identify patients with autoimmune pulmonary alveolar proteinosis (APAP). However, it is not clear which of the bio
Externí odkaz:
https://doaj.org/article/354038660885429c89622bd4ec94a678
Autor:
Jiu-Wu Bai, Jian-nan Huang, Shen-yun Shi, Ai Ge, Hai-wen Lu, Xiao-li Sun, Shu-yi Gu, Shuo Liang, Ke-bin Cheng, Xin-lun Tian, Yong-long Xiao, Kai-feng Xu, Jin-Fu Xu
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
BackgroundThe high-resolution computed tomography (HRCT) score is an important component of the severity and prognosis score of pulmonary alveolar proteinosis (SPSP). However, the HRCT score in SPSP only considers the extent of opacity, which is insu
Externí odkaz:
https://doaj.org/article/c0bee96c55034868aa7c29416f4fa87e
Autor:
Maki Asami-Noyama, Kosuke Ito, Misa Harada, Yukari Hisamoto, Yoshie Kunihiro, Eiji Ikeda, Tasuku Yamamoto, Junki Suizu, Ayumi Fukatsu, Syuichiro Ohata, Yoriyuki Murata, Keiji Oishi, Yoshikazu Yamaji, Nobutaka Edakuni, Tomoyuki Kakugawa, Tsunahiko Hirano, Kazuto Matsunaga
Publikováno v:
Respiratory Medicine Case Reports, Vol 44, Iss , Pp 101862- (2023)
Herein, we report the case of a 73-year-old woman with an occupational history of plaster grinding who developed autoimmune pulmonary alveolar proteinosis (PAP) during the treatment of fibrotic hypersensitivity pneumonitis with steroids and immunosup
Externí odkaz:
https://doaj.org/article/b0d061c6066d4596bd04783aad45a8ea
Autor:
Hillard M. Lazarus, Katherine Pitts, Tisha Wang, Elinor Lee, Elizabeth Buchbinder, Michael Dougan, David G. Armstrong, Robert Paine, Carolyn E. Ragsdale, Timothy Boyd, Edwin P. Rock, Robert Peter Gale
Publikováno v:
Frontiers in Immunology, Vol 13 (2023)
IntroductionEndogenous granulocyte-macrophage colony-stimulating factor (GM-CSF), identified by its ability to support differentiation of hematopoietic cells into several types of myeloid cells, is now known to support maturation and maintain the met
Externí odkaz:
https://doaj.org/article/628d7532ee3142388262f636c3a91400