genetics

Analysis of the subcellular localization in BMPR2 gene in pulmonary arterial hypertension
Guillermo Pousada, Vincenzo Lupo, Adolfo Baloira, Carmen Espinós, Diana Valverde

European Respiratory Journal Sep 2016, 48 (suppl 60) PA5103; DOI: 10.1183/13993003.congress-2016.PA5103
A new molecular genetic diagnostic approach for pulmonary arterial hypertension
Christina Eichstaedt, Jie Song, Rebecca Rodríguez Viales, Nicola Benjamin, Satenik Harutyunova, Christine Fischer, Ekkehard Grünig, Katrin Hinderhofer

European Respiratory Journal Sep 2016, 48 (suppl 60) PA5093; DOI: 10.1183/13993003.congress-2016.PA5093
Clinical phenotypes and outcomes of pulmonary veno-occlusive disease in carriers of bi-allelic EIF2AK4 mutations
David Montani, Barbara Girerd, David Amar, Xavier Jais, Laurent Savale, Peter Dorfmuller, Andrei Seferian, Edmund Lau, Mélanie Eyries, Jérome Lepavec, Florence Parent, Florent Soubrier, Elie Fadel, Olivier Sitbon, Gérald Simonneau, Marc Humbert

European Respiratory Journal Sep 2016, 48 (suppl 60) PA5096; DOI: 10.1183/13993003.congress-2016.PA5096
GST genes defects contribution into asthma phenotypes characteristics in children
Mary Kuropatenko, Natalia Platonova, Zarrina Azamova, Elizaveta Agapova, Ludmila Zhelenina

European Respiratory Journal Sep 2016, 48 (suppl 60) PA4371; DOI: 10.1183/13993003.congress-2016.PA4371
Study of the correlations between FENO and atopic status, blood eosinophils, FCER2 mutation, and asthma control in Vietnamese children
Hanh Nguyen Thi Bich, Huong Duong Thi Ly, Thom Vu Thi, Nhung Pham Thi Hong, Long Dinh Doan, Timothy J. Craig, Huong Le Thi Minh, Sy Duong-Quy

European Respiratory Journal Sep 2016, 48 (suppl 60) PA4378; DOI: 10.1183/13993003.congress-2016.PA4378
Defining uncontrolled childhood asthma in the global PiCA consortium
Niloufar Farzan, Susanne J. Vijverberg, Anand K. Andiappan, Natalia Blanca-Lopez, Klaus Bønnelykke, Paloma Campo, Glorisa Canino, Bruce Carleton, Juan C. Celedón, Fook Tim Chew, Michelle M. Cloutier, Denise Daley, Nicole Dijk, Liesbeth Duijts, Carlos Flores, Erick Frono, Daniel B. Hawcutt, Michael Kabesch, Gerard H. Koppelman, Vangelis G. Manolopoulos, Erik Melén, Somnath Mukhopadhyay, Sara Nilsson, Colin N. Palmer, Maria Pino-Yanes, Munir Pirmohamed, Uros Potocnik, Jan A. Raaijmakers, Katja Repnik, Maximilian Schieck, Rosalind Smyth, Patricia Soares, Csaba Szalai, Kelan G. Tantisira, Stephen Turner, Marc P. van der Schee, Katia M. Verhamme, Anke H. Maitland-van der Zee

European Respiratory Journal Sep 2016, 48 (suppl 60) PA4388; DOI: 10.1183/13993003.congress-2016.PA4388
Alpha-1 antitrypsin deficiency prevalence in COPD patients in a specialized hospital in Buenos Aires, Argentina
Guillermo Menga, Patricia Sorroche, María Soledad Saez, Juan José Moncalvo, Martín Eduardo Fernandez

European Respiratory Journal Sep 2016, 48 (suppl 60) PA4226; DOI: 10.1183/13993003.congress-2016.PA4226
Heritability in general and specific atopy: A twin study
Howraman Meteran, Linnea Skov, Vibeke Backer, Kirsten Ohm Kyvik, Simon Francis Thomsen

European Respiratory Journal Sep 2016, 48 (suppl 60) PA4189; DOI: 10.1183/13993003.congress-2016.PA4189
Relation of IL-33 and PSMA6 gene polymorphisms in asthma patients
Edita Gasiuniene, Zivile Zemeckiene, Raimundas Sakalauskas, Brigita Sitkauskiene

European Respiratory Journal Sep 2016, 48 (suppl 60) PA4188; DOI: 10.1183/13993003.congress-2016.PA4188
Phenotype heterogeneity in a familial “brain lung thyroid syndrome” related to a novel NKX-2.1 mutation
Nadia Nathan, Raphaël Borie, Sophie Jovien, Diane Doummar, Malek Louha, Julie Beucher, Mélanie Henriat, Estelle Breton, Annick Clement

European Respiratory Journal Sep 2016, 48 (suppl 60) PA3889; DOI: 10.1183/13993003.congress-2016.PA3889

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