Source: Eur Respir J 2009; 33: 1510-1512



Rating:

Share or cite this content

Citations should be made in the following way:
Sundaram S., Tasker A. D., Morrell N. W.. Familial spontaneous pneumothorax and lung cysts due to a Folliculin exon 10 mutation. Eur Respir J 2009; 33: 1510-1512

Member's Comments

No comment yet.

Related content which might interest you: Novel mutations in the folliculin gene associated with spontaneous pneumothorax Source: Eur Respir J 2008; 32: 1316-1320 Year: 2008 Prevalence of Birt–Hogg–Dubé syndrome in patients with apparently primary spontaneous pneumothorax Source: Eur Respir J 2015; 45: 1191-1194 Year: 2015 Spontaneous pneumothorax can be associated with TGFBR2 mutation Source: Eur Respir J 2015; 46: 1832-1835 Year: 2015 Familial interstitial lung disease and ABCA3 gene Gly964Asp mutation Source: Annual Congress 2010 - Pathogenesis of diffuse parenchymal lung disease Year: 2010 The lower pleural covering technique for Birt-Hogg-Dubé syndrome (BHDS) with recurrent pneumothorax Source: International Congress 2015 – Risk assessment and prevention of complications in thoracic surgery Year: 2015 Surgery for secondary pneumothorax caused by Hermansky–Pudlak syndrome Source: Eur Respir J 2014; 44: 1715-1717 Year: 2014 Intersitial lung disease in chlidren with mutation in the  SFTPC and SFPTB gene: A two case report Source: International Congress 2017 – Pulmonary infection and inflammation Year: 2017 Lung hypoplasia in asphyxiating thoracic dysplasia (jeune syndrome): report of 3 cases Source: Eur Respir J 2003; 22: Suppl. 45, 309s Year: 2003 Multiple cystic lung diseases Source: Eur Respir Mon 2011; 54: 46-83 Year: 2011 Pulmonary fibrosis in dyskeratosis congenita with TINF2 gene mutation Source: Eur Respir J 2013; 42: 1757-1759 Year: 2013 First heterozygous NOP10 mutation in familial pulmonary fibrosis Source: Eur Respir J, 55 (6) 1902465; 10.1183/13993003.02465-2019 Year: 2020 Pulmonary fibrosis in non-mutation carriers of families with short telomere syndrome gene mutations. Source: Virtual Congress 2021 – Genetics and translational aspects of idiopathic pulmonary fibrosis Year: 2021 A case report: hyper-IgE syndrome; a rare cause of recurrent pneumonia and pneumatocele Source: Eur Respir J 2003; 22: Suppl. 45, 248s Year: 2003 Hereditary pulmonary alveolar proteinosis caused by recessive CSF2RB mutations Source: Eur Respir J 2011; 37: 201-204 Year: 2011 Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis Source: Eur Respir J 2015; 46: 474-485 Year: 2015 Cancer gene mutations in congenital pulmonary airway malformation patients Source: ERJ Open Res, 5 (1) 00196-2018; 10.1183/23120541.00196-2018 Year: 2019 Ehlers-Danlos syndrome type IV with few extrathoracic findings: a newly recognized point mutation in the COL3A1 gene Source: Eur Respir J 2002; 19: 195-198 Year: 2002 Sftpc mutations are a common cause of adult familial idiopathic interstitial pneumonia Source: Annual Congress 2009 - Pathogenesis of pulmonary fibrosis Year: 2009 Hermansky-Pudlak syndrome type 4 with interstitial pneumonia Source: Annual Congress 2013 –Diffuse parenchymal lung disease I Year: 2013 Effusion, pneumothorax and interstitial syndrome Source: ERS Course 2016 - Skills course on thoracic ultrasound Year: 2016