HuGE Literature Finder
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| Prevalence of CFTR variants in PID patients with bronchiectasis - an important modifying co-factor. The Journal of allergy and clinical immunology 2023 2 . Lawless Dylan, Allen Hana Lango, Thaventhiran James E D, Goddard Sarah, Burren Oliver S, Robson Evie, , Peckham Daniel, Smith Kenneth G C, Savic Sini |
| Occurrence of Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations in Patients with Allergic Bronchopulmonary Aspergillosis Complicating Asthma. Mycopathologia 2022 4 187 (2-3): 147-155. Kanaujia Rimjhim, Arora Amit, Chakrabarti Arunaloke, Rudramurthy Shivaprakash M, Agarwal Rite |
| Characterization of clinical and genetic spectrum of Chinese patients with cystic fibrosis. Orphanet journal of rare diseases 2020 6 15 (1): 150. Liu Keqiang, Xu Wenshuai, Xiao Meng, Zhao Xinyue, Bian Chun, Zhang Qianli, Song Jiaxing, Chen Keqi, Tian Xinlun, Liu Yaping, Xu Kai-Feng, Zhang X |
| Morbidity and mortality in carriers of the cystic fibrosis mutation CFTR Phe508del in the general population. The European respiratory journal 2020 5 56 (3): . Çolak Yunus, Nordestgaard Børge G, Afzal Shoa |
| Next-generation sequencing for identifying genetic mutations in adults with bronchiectasis. Journal of thoracic disease 2018 May 10 (5): 2618-2630. Guan Wei-Jie, Li Jia-Cheng, Liu Fang, Zhou Jian, Liu Ya-Ping, Ling Chao, Gao Yong-Hua, Li Hui-Min, Yuan Jing-Jing, Huang Yan, Chen Chun-Lan, Chen Rong-Chang, Zhang Xue, Zhong Nan-Sh |
| F508del CFTR gene mutation in patients with allergic bronchopulmonary aspergillosis. The Journal of asthma : official journal of the Association for the Care of Asthma 2017 Oct 1-7. Gamaletsou Maria N, Hayes Gemma, Harris Chris, Brock Joanna, Muldoon Eavan G, Denning David |
| Frequency of Genotype With ?F508 Mutation in CFTR Gene Among Iranian Cystic Fibrosis Patients With Pancreatic Insufficiency. Iranian journal of pediatrics 2015 Dec 25 (6): e3419. Khodadad Ahmad, Elahi Elaheh, Bani Hassani Setareh Sadat, Rouhani Pejman, Sadeghi Bamdad, Rezaei Ni |
| p.Arg75Gln, a CFTR variant involved in the risk of CFTR-related disorders? Journal of human genetics 2014 Apr 59 (4): 206-10. Martinez Brigitte, Heller Marion, Gaitch Natacha, Hubert Dominique, Burgel Pierre-Regis, Levy Philippe, Girodon Emmanuelle, Bienvenu Thier |
| Poor survival in rheumatoid arthritis associated with bronchiectasis: a family-based cohort study. PloS one 2014 9 (10): e110066. Puéchal Xavier, Génin Emmanuelle, Bienvenu Thierry, Le Jeunne Claire, Dusser Daniel |
| Analysis of CFTR Gene Variants in Idiopathic Bronchiectasis in Serbian Children. Pediatric allergy, immunology, and pulmonology 2013 Jun 26 (2): 93-98. Milosevic Katarina, Nikolic Aleksandra, Divac Rankov Aleksandra, Ljujic Mila, Nestorovic Branimir, Radojkovic Dragi |
| Phenotypic expression of the p.Leu1077Pro CFTR mutation in Sicilian cystic fibrosis patients. BMC research notes 2013 6 (1): 461. Parisi Giuseppe Fabio, Cutello Silvia, Di Dio Giovanna, Rotolo Novella, La Rosa Mario, Leonardi Salvato |
| Mutations of the cystic fibrosis gene in patients with bronchiectasis associated with rheumatoid arthritis. Annals of the rheumatic diseases 2011 Apr 70 (4): 653-9. Puéchal Xavier, Bienvenu Thierry, Génin Emmanuelle, Berthelot Jean-Marie, Sibilia Jean, Gaudin Philippe, Marcelli Christian, Lasbleiz Sandra, Michou Laëtitia, Cornélis François, Kahan André, Dusser Daniel |
| Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis. American journal of respiratory and critical care medicine 2010 May 181 (10): 1078-84. Bienvenu Thierry, Sermet-Gaudelus Isabelle, Burgel Pierre-Regis, Hubert Dominique, Crestani Bruno, Bassinet Laurence, Dusser Daniel, Fajac Isabel |
| Non-classic cystic fibrosis associated with D1152H CFTR mutation. Clinical genetics 2010 Apr 77 (4): 355-64. Burgel P-R, Fajac I, Hubert D, Grenet D, Stremler N, Roussey M, Siret D, Languepin J, Mely L, Fanton A, Labbé A, Domblides P, Vic P, Dagorne M, Reynaud-Gaubert M, Counil F, Varaigne F, Bienvenu T, Bellis G, Dusser |
| Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Asians with chronic pulmonary disease: a pilot study. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2006 Aug 5 (3): 159-64. Ngiam Nicola S P, Chong Samuel S, Shek Lynette P C, Goh Denise L M, Ong K C, Chng S Y, Yeo G H, Goh Daniel Y |
| Indirect CFTR mutation identification by PCR/OLA anomalous electropherograms. Genetic testing 2005 9 (4): 285-91. Stanziale Pietro, Savino Maria, De Bonis Patrizia, Granatiero Matteo, Zelante Leopoldo, Bisceglia Lui |
| Bronchiectasis in adult patients: an expression of heterozygosity for CFTR gene mutations? Clinical genetics 2004 Jun 65 (6): 490-5. Casals T, De-Gracia J, Gallego M, Dorca J, Rodríguez-Sanchón B, Ramos M D, Giménez J, Cisteró-Bahima A, Olveira C, Estivill |
| CFTR gene mutations--including three novel nucleotide substitutions--and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary disease. Human genetics 2001 Mar 108 (3): 216-21. Tzetis M, Efthymiadou A, Strofalis S, Psychou P, Dimakou A, Pouliou E, Doudounakis S, Kanavakis |
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- Page last updated:Mar 29, 2023
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