Zobrazeno 1 - 10
of 228
pro vyhledávání: '"pulmonary cysts"'
Autor:
Yongfeng Luo, Ke Cao, Joanne Chiu, Hui Chen, Hong-Jun Wang, Matthew E Thornton, Brendan H Grubbs, Martin Kolb, Michael S Parmacek, Yuji Mishina, Wei Shi
Publikováno v:
eLife, Vol 12 (2024)
Abnormal lung development can cause congenital pulmonary cysts, the mechanisms of which remain largely unknown. Although the cystic lesions are believed to result directly from disrupted airway epithelial cell growth, the extent to which developmenta
Externí odkaz:
https://doaj.org/article/310cc91eef7547f0b2c6ff8d0cb9222f
Publikováno v:
Respirology Case Reports, Vol 12, Iss 3, Pp n/a-n/a (2024)
Abstract Birt–Hogg–Dubé syndrome (BHD) is an inherited autosomal dominant condition caused by germline mutations in the FLCN gene, mapped to chromosome 17p11.2. Typical manifestations include pulmonary cysts, spontaneous pneumothorax, fibrofolli
Externí odkaz:
https://doaj.org/article/77cda1c04172403e93a5b1bc66ac29c8
Akademický článek
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Publikováno v:
Cancer Management and Research, Vol Volume 14, Pp 2373-2377 (2022)
Yibing Xie,1,2 Dongmei Zhang,3 Huanfen Zhao,4 Shaoyang Lei,2 Hua Zhang,5 Shuqian Zhang2 1Department of Graduate School, Hebei North University, Zhangjiakou, People’s Republic of China; 2Department of Radiology, Hebei General Hospital, Shijiazhuang,
Externí odkaz:
https://doaj.org/article/c69dc029d50040809deb974055c1e12a
Akademický článek
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Autor:
Balasubramanian Gurumurthy, Sudha Kiran Das, Rudresh Hiremath, Sachin Shetty, Aniketh Hiremath, Thasmai Gowda
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 52, Iss 1, Pp 1-13 (2021)
Abstract Background The typical CT manifestations of COVID-19 pneumonia include ground-glass opacity (GGO) with or without consolidation and superimposed interlobular septal thickening. These are often rounded in morphology and frequently bilateral,
Externí odkaz:
https://doaj.org/article/aed52fdf4a2b4a57a52aa298ee33407d
Autor:
Maxim Avanesov, Lennart Well, Azien Laqmani, Thorsten Derlin, Vincent M. Riccardi, Gerhard Adam, Victor-Felix Mautner, Johannes Salamon
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-10 (2021)
Abstract Background Diffuse interstitial lung disease have been described in Neurofibromatosis type 1 (NF1), but its diversity and prevalence remain unknown. The aim of this study was to assess the prevalence and characteristics of (NF1)-associated l
Externí odkaz:
https://doaj.org/article/3e4463396ede43d98f85c412704dc1a8
Publikováno v:
Radiology Case Reports, Vol 15, Iss 9, Pp 1464-1467 (2020)
Birt-Hogg-Dubé syndrome (BHDS) is a rare autosomal-dominant inherited disease. Typical clinical features include skin lesions, pulmonary cysts, and renal tumors. However, the syndrome remains to be underdiagnosed as a result of its heterogeneous cli
Externí odkaz:
https://doaj.org/article/b08614a3dbf845e2934e41a773a60c05
Akademický článek
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Autor:
Yuki Yabuuchi, Hitomi Goto, Mizu Nonaka, Hiroaki Tachi, Tatsuya Akiyama, Naoki Arai, Hiroaki Ishikawa, Kentaro Hyodo, Kenji Nemoto, Yukiko Miura, Isano Hase, Shingo Usui, Shuji Oh-ishi, Kenji Hayashihara, Takefumi Saito, Tatsuya Chonan
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-5 (2020)
Abstract Background Marfan Syndrome (MFS) is a heritable connective tissue disorder with a high degree of clinical variability including respiratory diseases; a rare case of MFS with massive intrathoracic bleeding has been reported recently. Case pre
Externí odkaz:
https://doaj.org/article/93f922dde05c4f4bbfe6e07da3a0e9a0