Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Robert L. Vender"'
Publikováno v:
Clinical Infection and Immunity. 6:6-10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c542c76c6d3efe5ec940050cfbf27fe
https://doi.org/10.14740/cii126
https://doi.org/10.14740/cii126
Autor:
Robert L. Vender, Robert J. Vender
Publikováno v:
Journal of Clinical Medicine Research
Background: Blood cultures are obtained clinically to confirm site and source of acute infection as well as to guide effective antibiotic therapies. Patients with cystic fibrosis (CF) are at risk for blood stream infection (BSI) as identified from po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fc4cc7c9c24dd233862f089ab1db642
https://doi.org/10.14740/jocmr2764w
https://doi.org/10.14740/jocmr2764w
Autor:
Richard B. Moss, Jonathan E. Spahr, Carol Conrad, Peter H. Michelson, James Lymp, C. Dunn, John P. Clancy, Z. Davies, Leonore A. Herzenberg, Ronald C. Rubenstein, Marie E. Egan, Christopher H. Goss, L. Quittell, David P. Nichols, Robert L. Vender, Rabindra Tirouvanziam, Valeria Thompson, Barbara A. Chatfield, Veena B. Antony
Publikováno v:
Journal of Cystic Fibrosis. 14(2):219-227
To evaluate the effects of oral N-acetylcysteine (NAC), which replenishes systemic glutathione, on decreasing inflammation and improving lung function in CF airways.A multicenter, randomized, double-blind proof of concept study in which 70 CF subject
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40b09addd0c7edc3095f9e6d38042f31
Autor:
Lucina M Vender, Robert L. Vender
Publikováno v:
Journal of Nursing & Care.
Robert L Vender1* and Lucina M Vender2 1Department of Medicine, Pulmonary, Allergy, Critical Care Medicine, Penn State Milton S. Hershey Medical Center, USA 2Instructor of Nursing, College of Nursing, Pennsylvania State University, USA *Corresponding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::403a37f7b2002f918f1c70c00a1776ea
https://doi.org/10.4172/2167-1168.1000239
https://doi.org/10.4172/2167-1168.1000239
Publikováno v:
Journal of Clinical Medicine Research
Background Cystic fibrosis (CF) is a monogenetic autosomal recessive multi-organ disease affecting approximately 50,000 patients worldwide. Overall median survival is continually increasing but pulmonary disease remains the most common cause of death
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc05b5ff130761234cdacbd1df6a7425
http://europepmc.org/articles/PMC3279481
http://europepmc.org/articles/PMC3279481
Autor:
Randall L. Rosenblatt, Daniel Rosenbluth, Marcia Katz, Henry L. Dorkin, Patrick A. Flume, Moira L. Aitken, Michelle S. Howenstine, Manu Jain, David C. McGiffin, Joseph M. Pilewski, Ahmet Uluer, Craig W. Lillehei, Beryl J. Rosenstein, Hector H. Gutierrez, Terry B. White, James D. Acton, Randall K. Young, Thomas M. Egan, Kathryn A. Sabadosa, Steven Strausbaugh, Mary K Lester, Sally E. Mitchell, Douglas S. Holsclaw, Bruce C. Marshall, Mike Mulligan, David M. Orenstein, Donna Beth Willey-Courand, Peter J. Mogayzel, Susanna A. McColley, Souheil Saddekni, Melissa Chin, Lynne M. Quittell, Paul Mohabir, Christopher M. Oermann, James R. Yankaskas, Michael P. Boyle, Robert J. Kuhn, R. Duane Davis, Jill Fleige, Michael J. Rock, Elizabeth Tullis, Anne M Downs, James L. Cunningham, Peter J Murphy, John L. Colombo, Linda L. Wolfenden, Thomas W. Ferkol, Patricia M. Joseph, Jeffrey S. Wagener, George Z. Retsch-Bogart, Christopher H. Goss, Karen A. Robinson, Carlos Milla, Felix Ratjen, Michael S. Schechter, Patricia E. Burrows, Aruna Sannuti, Charles B. Huddleston, Robert L. Vender, Leslie Hazle, Mark J. Sands, Charles T. Burke, Wickii T. Vigneswaran, Ronald C. Rubenstein, Guillermo A. doPico, Jerry A. Nick, Wyn Hoover, Mark H. Wholey
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 182:298-306
Cystic fibrosis (CF) is a recessive genetic disease characterized by dehydration of the airway surface liquid and impaired mucociliary clearance. As a result, individuals with the disease have difficulty clearing pathogens from the lung and experienc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee82205e6b63ce9b3731b135f84a4850
https://doi.org/10.1164/rccm.201002-0157oc
https://doi.org/10.1164/rccm.201002-0157oc
Publikováno v:
Respiratory Medicine CME. 3:156-159
Cystic fibrosis (CF) is a genetically inherited autosomal recessive disease characterized by dehydration of the airway surface liquid and impaired mucociliary clearance leading to chronic respiratory infections, bronchiectasis and ultimately death fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb7206de7e99037885de3fac47e114d9
https://doi.org/10.1016/j.rmedc.2009.09.008
https://doi.org/10.1016/j.rmedc.2009.09.008
Publikováno v:
Amyotrophic Lateral Sclerosis. 7:107-111
Respiratory complications are common in patients with amyotrophic lateral sclerosis (ALS) with respiratory failure representing the most common cause of death. Ineffective airway clearance resultant from deficient cough frequently contributes to thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::400abcbac373a2f8d5da3f585162430a
https://doi.org/10.1080/14660820600640570
https://doi.org/10.1080/14660820600640570
Autor:
Robert L. Vender, Dan A. Galvan, Manuel F. Betancourt, David C. Frankenfield, Erik Lehman, Christopher Harrell
Publikováno v:
Journal of critical care. 29(2)
Objective The measurement of dead space to tidal volume fraction (Vd/Vt) using various methodologies has been shown to be a reliable predictor of mortality in critically ill patients. In this study, we evaluated the correlation of a validated equatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f838c9246f1dec53f3797fce65c45ac1
https://pubmed.ncbi.nlm.nih.gov/24581935
https://pubmed.ncbi.nlm.nih.gov/24581935
Autor:
Robert L. Vender
Publikováno v:
Chest. 106:236-243
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00341b21cc16116ec144c3d788258b7e
https://doi.org/10.1378/chest.106.1.236
https://doi.org/10.1378/chest.106.1.236