Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Raymond K. Lyrene"'
Autor:
Raymond K. Lyrene, Martin L. Bauer
Publikováno v:
Pediatric Pulmonology. 28:94-100
Chronic pulmonary aspiration (CPA) causes significant morbidity, but is underdiagnosed because of difficulties in establishing a diagnosis. The lipid-laden macrophage index (LLMI) is said to differentiate between those with and without CPA. Records o
Autor:
Jian-Yun Dong, Co-Investigators: Raymond A. Frizzell, James J. Logan, Principal Investigators: Eric J. Sorscher, P. L. Feigner, Lynn Walker, Raymond K. Lyrene, Sadis Matalon, Brian J. Wiatrak, Michael D. DuVall, Investigators: Zsuzsa Bebok
Publikováno v:
Human Gene Therapy. 5:1259-1277
SCIENTIFIC ABSTRACT Cystic fibrosis (CF) is a common, lethal, inherited disease among Caucasian children and young adults. While the pathophysiology of CF includes many organ systems (e.g., gastrointestinal, reproductive, endocrine) the predominant c
Autor:
Lyle L. Moldawer, Eric J. Sorscher, Nicki Koppersmith, Nancy Wooldridge, Jeanette Lee, Joy Atchison, J.P. Clancy, Ramin B. Arani, Valerie Eubanks, Christopher M. Makris, Raymond K. Lyrene
Publikováno v:
The Journal of pediatrics. 140(4)
Malnutrition is a negative prognostic indicator in patients with cystic fibrosis (CF) and may accentuate pulmonary decline. We tested whether megestrol acetate would have beneficial effects on growth in patients with CF and pancreatic insufficiency.W
Autor:
Jeong S. Hong, Fadel E. Ruiz, Julie R. Jones, Eric J. Sorscher, David M. Bedwell, Zsuzsa Bebok, Heather Greer, Lynn Walker, Raymond K. Lyrene, John P. Clancy, Maurizio Macaluso, Christopher L. King, Lisa Wing
Publikováno v:
American journal of respiratory and critical care medicine. 163(7)
Here we report the effects of gentamicin treatment on cystic fibrosis transmembrane regulator (CFTR) production and function in CF airway cells and patients with CF with premature stop mutations. Using immunocytochemical and functional [6-methoxy-N-
Autor:
Eric J, Sorscher, James J, Logan, Raymond A, Frizzell, Raymond K, Lyrene, Zsuzsa, Bebok, J Y, Dong, M D, Duvall, P L, Felgner, Sadis, Matalon, Lynn, Walker, Brian J, Wiatrak
Publikováno v:
Human gene therapy. 5(10)
Autor:
Barry M. Gray, J. E.P. Sams, Joseph B. Philips, Gwendolyn B. Graybar, Guillermo Godoy, Elaine S. Barefield, Raymond K. Lyrene
Publikováno v:
Pediatric Research. 23:81-85
Group B β-hemolytic Streptotocci cause pulmonary hypertension when injected into animals and may precipitate the persistent pulmonary hypertension syndrome in infected human neonates. We used chronically instrumented piglets to study the effects of
Autor:
Joseph B. Philips, Raymond K. Lyrene
Publikováno v:
Clinics in Perinatology. 11:565-579
It is clear that prostaglandins and related compounds are important in the physiology and pathophysiology of the perinatal pulmonary circulation. This article focuses on what is known about prostaglandin-related compounds (PRC) in the pulmonary circu
Publikováno v:
The Journal of Pediatrics. 95:848-851
IT IS COMMONLY STATED that there is an increasing incidence of chronic pulmonary disease occurring in newborn infants within neonata l intensive care units. Substantive information on incidence, either past or present, is difficult to obtain since th
Autor:
Joseph B. Philips, Raymond K. Lyrene
Publikováno v:
Clinics in Perinatology. 11:551-564
This article describes the anatomy and physiology of the fetal, transitional, and neonatal circulations and then reviews our current state of knowledge about the many factors that work in concert to govern pulmonary vascular resistance.
Publikováno v:
The Journal of Pediatrics. 106:669-672