G
G.A. Lombard
Researcher at Ochsner Medical Center
Publications - 6
Citations - 331
G.A. Lombard is an academic researcher from Ochsner Medical Center. The author has contributed to research in topics: Cystic fibrosis & Lung transplantation. The author has an hindex of 2, co-authored 6 publications receiving 297 citations. Previous affiliations of G.A. Lombard include LSU Health Sciences Center New Orleans.
Papers
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Journal ArticleDOI
CFTR Expression in human neutrophils and the phagolysosomal chlorination defect in cystic fibrosis.
Richard G. Painter,Vincent G. Valentine,Nicholas A. Lanson,Kevin Leidal,Qiang Zhang,G.A. Lombard,Connie Thompson,Anand Viswanathan,William M. Nauseef,Guangdi Wang,Guoshun Wang +10 more
TL;DR: Evidence is provided which suggests that CFTR channel expression in neutrophils and its dysfunction affect neutrophil chlorination of phagocytosed bacteria.
Journal ArticleDOI
Post-operative infections in cystic fibrosis and non-cystic fibrosis patients after lung transplantation
Ryan W. Bonvillain,Vincent G. Valentine,G.A. Lombard,S.G. LaPlace,Gundeep Dhillon,Guoshun Wang +5 more
TL;DR: The normal lungs implanted into CF patients had significantly higher susceptibility to Pseudomonas infections than those into non-CF patients, suggesting that defective innate immunity outside the lungs contributes to CF lung pathogenesis.
Journal ArticleDOI
Metabolic consequences of lung transplantation
TL;DR: The incidences and likelihood ratios of developing the aforementioned metabolic consequences with respect to underlying pulmonary diagnosis and metabolic complications that developed after LT are described.
Journal ArticleDOI
161: Comparison of infection profiles from cystic fibrosis (CF) and non-CF patients after lung transplantation
Journal ArticleDOI
317: A single-institution study evaluating the utility of surveillance bronchoscopy following lung transplantation
Vincent G. Valentine,David Weill,G.A. Lombard,S.G. LaPlace,Leonardo Seoane,D.E. Taylor,Gundeep Dhillon +6 more
TL;DR: A restricted T cell repertoire that is maintained over time is observed in the setting of lung transplantation, and the molecular profile mirrors the restricted clonal T cell infiltrates seen in autoimmune disease.