Zobrazeno 1 - 10
of 12
pro vyhledávání: '"K. Akaya Smith"'
Autor:
Jeff Min, Dina H. Appleby, Robyn L. McClelland, Jasleen Minhas, John H. Holmes, Ryan J. Urbanowicz, Steven C. Pugliese, Jeremy A. Mazurek, K. Akaya Smith, Jason S. Fritz, Harold I. Palevsky, Jude Moutchia Suh, Nadine Al-Naamani, Steven M. Kawut
Publikováno v:
Ann Am Thorac Soc
RATIONALE: The population of patients with pulmonary arterial hypertension (PAH) has evolved over time from predominantly young White women to an older, more racially diverse and obese population. Whether these changes are reflected in clinical trial
Autor:
Breanne E. McCarthy, Robyn L. McClelland, Dina H. Appleby, Jude S. Moutchia, Jasleen K. Minhas, Jeff Min, Jeremy A. Mazurek, K. Akaya Smith, Jason S. Fritz, Steven C. Pugliese, Ryan J. Urbanowicz, John H. Holmes, Harold I. Palevsky, Steven M. Kawut, Nadine Al-Naamani
Publikováno v:
Chest. 162:436-447
Autor:
Breanne E, McCarthy, Robyn L, McClelland, Dina H, Appleby, Jude S, Moutchia, Jasleen K, Minhas, Jeff, Min, Jeremy A, Mazurek, K Akaya, Smith, Jason S, Fritz, Steven C, Pugliese, Ryan J, Urbanowicz, John H, Holmes, Harold I, Palevsky, Steven M, Kawut, Nadine, Al-Naamani
Publikováno v:
Chest. 162(2)
Obesity is increasingly prevalent in pulmonary arterial hypertension (PAH) but is associated with improved survival, creating an "obesity paradox" in PAH. It is unknown if the improved outcomes could be attributable to obese patients deriving a great
Autor:
Jeremy A. Mazurek, Harold I. Palevsky, David A. Mankoff, Margaret R. MacLean, Angela DeMichele, Margaret F. Doyle, Diane Pinder, Steven M. Kawut, Nadine Al-Naamani, Jason S. Fritz, Amber McCormick, K. Akaya Smith
Publikováno v:
Ann Am Thorac Soc
Anastrozole in Pulmonary Arterial Hypertension. A Randomized, Double-Blind, Placebo-controlled Trial
Autor:
Harold I. Palevsky, Corey E. Ventetuolo, James R. Klinger, Kathleen J. Propert, Frank Z. Stanczyk, Anjali Vaidya, Mary Whittenhall, Amy Palmisciano, M. Patel, Diane Pinder, Bonnie Ky, Russell P. Tracy, K. Akaya Smith, Angela DeMichele, Jason S. Fritz, Steven M. Kawut, Christine Archer-Chicko
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 195:360-368
Rationale: The aromatase inhibitor anastrozole blocks the conversion of androgens to estrogen and blunts pulmonary hypertension in animals, but its efficacy in treating patients with pulmonary arterial hypertension (PAH) is unknown.Objectives: We aim
Autor:
K. Akaya Smith, Jason S. Fritz
Publikováno v:
Chest. 150:705-713
Pulmonary hypertension (PH) is an increasingly recognized cause of morbidity and mortality, and in the past 20 years, there has been a rapid expansion in research and available therapies. Although it is defined quite simply as a mean pulmonary arteri
Autor:
Haochang Shou, Christine Archer-Chicko, Harold I. Palevsky, Diane Pinder, Marilyn S. Sommers, Anjali Vaidya, Steven M. Kawut, Danielle Dubow, Lea Ann Matura, K. Akaya Smith, Jason S. Fritz
Publikováno v:
Chest. 150:46-56
Background Fatigue is a common symptom in patients with pulmonary arterial hypertension (PAH); however, the impact of fatigue on daily physical activity in PAH is unknown. Accelerometry is a validated measure for assessing physical activity. We hypot
Autor:
Diane Pinder, Amy J. Palmisicano, R. Graham Barr, Joao A.C. Lima, Harold I. Palevsky, Steven M. Kawut, Christopher J Mullin, Christine Archer-Chicko, Andrew Foderaro, David A. Bluemke, Grayson L. Baird, James R. Klinger, Thomas Walsh, Ioana R. Preston, Pamela Ouyang, Jason S. Fritz, Kari E. Roberts, Nicholas S. Hill, Corey E. Ventetuolo, K. Akaya Smith, Mary Whittenhall
Publikováno v:
The European respiratory journal. 51(6)
High oestradiol (E2) and low dehydroepiandrosterone-sulfate (DHEA-S) levels are risk factors for pulmonary arterial hypertension (PAH) in men, but whether sex hormones are related to PAH in women is unknown.Post-menopausal women aged ≥55 years with
Autor:
Jonathan N. Menachem, Gregory S. Troutman, Julio A. Chirinos, Edo Y. Birati, E. Wilson Grandin, K. Akaya Smith, Payman Zamani, Steven M. Kawut, Anjali Vaidya, Jeremy A. Mazurek, Priyanka Bhattacharya, Paul R. Forfia, Stuart B. Prenner
Publikováno v:
Journal of Cardiac Failure. 25:S65
Background Pulmonary hypertension (PH) in the setting of left heart disease (PH-LHD) is the most common cause of PH in the general population, with a prevalence of up to 80% and is associated with high morbidity and mortality. We have previously demo
Autor:
Jason S, Fritz, K Akaya, Smith
Publikováno v:
Chest. 150(3)
Pulmonary hypertension (PH) is an increasingly recognized cause of morbidity and mortality, and in the past 20 years, there has been a rapid expansion in research and available therapies. Although it is defined quite simply as a mean pulmonary arteri