Search Results - "Hersh, C.P."

Unique and shared systemic biomarkers for emphysema in Alpha-1 Antitrypsin deficiency and chronic obstructive pulmonary disease by Serban, K.A., Pratte, K.A., Strange, C., Sandhaus, R.A., Turner, A.M., Beiko, T., Spittle, D.A., Maier, L., Hamzeh, N., Silverman, E.K., Hobbs, B.D., Hersh, C.P., DeMeo, D.L., Cho, M.H., Bowler, R.P.

“…Alpha-1 Antitrypsin (AAT) deficiency (AATD), the most common genetic cause of emphysema presents with unexplained phenotypic heterogeneity in affected…”
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A genome-wide analysis of the response to inhaled [β.sub.2]-agonists in chronic obstructive pulmonary disease by Hardin, M, Cho, M.H, McDonald, M.-L, Wan, E, Lomas, D.A, Coxson, H.O, MacNee, W, Vestbo, J, Yates, J.C, Agusti, A, Calverley, P.M.A, Celli, B, Crim, C, Rennard, S, Wouters, E, Bakke, P, Bhatt, S.P, Kim, V, Ramsdell, J, Regan, E.A, Make, B.J, Hokanson, J.E, Crapo, J.D, Beaty, T.H, Hersh, C.P

“…Short-acting [β.sub.2]-agonist bronchodilators are the most common medications used in treating chronic obstructive pulmonary disease (COPD). Genetic variants…”
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