Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Pneumothorax and FLCN[original query] |
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Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax. Clinical genetics 2008 Aug 74 (2): 178-83. Ren H-Z, Zhu C-C, Yang C, Chen S-L, Xie J, Hou Y-Y, Xu Z-F, Wang D-J, Mu D-K, Ma D-H, Wang Y, Ye M-H, Ye Z-R, Chen B-F, Wang C-G, Lin J, Qiao D, Yi |
Folliculin mutations are not associated with severe COPD. BMC medical genetics 2008 9 (1): 120. Cho Michael H, Klanderman Barbara J, Litonjua Augusto A, Sparrow David, Silverman Edwin K, Raby Benjamin |
FLCN intragenic deletions in Chinese familial primary spontaneous pneumothorax. American journal of medical genetics. Part A 2015 May 167A (5): 1125-33. Ding Yibing, Zhu Chengchu, Zou Wei, Ma Dehua, Min Haiyan, Chen Baofu, Ye Minhua, Pan Yanqing, Cao Lei, Wan Yueming, Zhang Wenwen, Meng Lulu, Mei Yuna, Yang Chi, Chen Shilin, Gao Qian, Yi Lo |
Birt-Hogg-Dubé syndrome in Korean: clinicoradiologic features and long term follow-up. The Korean journal of internal medicine 2018 10 34 (4): 830-840. Lee Joo Hee, Jeon Min Joo, Song Joon Seon, Chae Eun Jin, Choi Jin-Ho, Kim Gu-Hwan, Song Jin W |
Familial spontaneous pneumothorax: importance of screening for Birt-Hogg-Dubé syndrome. European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery 2019 6 57 (1): 39-45. Liu Yanguo, Xing Huajie, Huang Yu, Meng Shushi, Wang J |
The clinical characteristics of East Asian patients with Birt-Hogg-Dubé syndrome. Annals of translational medicine 2020 12 8 (21): 1436. Guo Ting, Shen Qinxue, Ouyang Ruoyun, Song Min, Zong Dandan, Shi Zhihui, Long Yingjiao, Chen Ping, Peng Ho |
Genetic Risk Factors for Spontaneous Pneumothorax in Birt-Hogg-Dubé Syndrome. Chest 2020 1 157 (5): 1199-1206. Sattler Elke C, Syunyaeva Zulfiya, Mansmann Ulrich, Steinlein Ortrud |
Novel folliculin gene mutations in Polish patients with Birt-Hogg-Dubé syndrome. Orphanet journal of rare diseases 2021 7 16 (1): 302. Radzikowska El?bieta, Lechowicz Urszula, Winek Jolanta, Opoka Lucy |
Genetic insight into Birt-Hogg-Dubé syndrome in Indian patients reveals novel mutations at FLCN. Orphanet journal of rare diseases 2022 4 17 (1): 176. Ray Anindita, Chattopadhyay Esita, Singh Richa, Ghosh Saurabh, Bera Arnab, Sarma Mridul, Munot Mahavir, Desai Unnati, Rajan Sujeet, Prabhudesai Pralhad, Prakash Ashish K, Roy Chowdhury Sushmita, Bhowmick Niladri, Dhar Raja, Udwadia Zarir F, Dey Atin, Mitra Subhra, Joshi Jyotsna M, Maitra Arindam, Roy Bidy |
Outstanding Characteristics of Birt-Hogg-Dube Syndrome in Korea. Diagnostics (Basel, Switzerland) 2023 6 13 (12): . Hye Jung Park, Yong Jun Choi, Chul Hwan Park, Tae Hoon Kim, Sung Soo Lee, Duk Hwan Moon, Kyung-A Lee, Sang Eun Lee, Moo Suk Park, Song Yee Kim, Yoon Soo Chang, Seok Jeong Lee, Ji Ye Jung, Ji-Ho Lee, Su Hwan Lee, Taehee Kim, Sung-Ryeol Kim, Kangjoon Kim, Min Kwang By |
Exons 1-3 deletion in FLCN is associated with increased risk of pneumothorax in Chinese patients with Birt-Hogg-Dubé syndrome. Orphanet journal of rare diseases 2023 5 18 (1): 115. Yue Wang, Mengru Cai, Xianliang Jiang, Guangyu Lv, Daiju Hu, Guofeng Zhang, Jinli Liu, Wei Wei, Jun Xiao, Bing Shen, Jay H Ryu, Xiaowen |
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- Page last updated:Mar 25, 2024
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