Zobrazeno 1 - 10
of 39
pro vyhledávání: '"M. E. Wohl"'
Publikováno v:
The Journal of Pediatrics. 145:689-692
To determine reproducibility of inflammatory marker concentrations in induced sputum from subjects with cystic fibrosis (CF), 15 nonexpectorating children, 6 to 13 years of age with mild CF lung disease, underwent 3 weekly sputum inductions with 3% s
Autor:
Henry L. Dorkin, David H. Christiansen, M. E. Wohl, Arnold L. Smith, Moira L. Aitken, Jay D. Eisenberg, Daniel V. Schidlow, Ivan R. Harwood, Bonnie W. Ramsey, Henry J. Fuchs, Robert W. Wilmott
Publikováno v:
The Journal of Pediatrics. 131:118-124
Objectives: To determine the effect of repeated doses of aerosolized recombinant human deoxyribonuclease (rhDNase) on the development of anti-rhDNase antibodies, acute allergic reactions, and pulmonary function in patients with cystic fibrosis. Desig
Autor:
John L. Carroll, B. R. Maddern, D. C. Givan, Claude Gaultier, I. T. Nathanson, Debra E. Weese-Mayer, S. L. Davidson Ward, Carol L. Rosen, S. J. England, Gerald M. Loughlin, P. Ferber, Robert T. Brouillette, Gabriel G. Haddad, B. E. Chipps, M. E. Wohl, George B. Mallory, N. F. Ferraro, B. T. Thach, L. J. Brooke
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 153:866-878
Autor:
Clifford J. Rosen, Meryl S. LeBoff, Catherine M. Gordon, M. E. Wohl, Emanuela Binello, A. A. Colin
Publikováno v:
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. 17(5)
Patients with cystic fibrosis (CF) are known to be at risk for early osteoporosis, and the mechanisms that mediate bone loss are still being delineated. The aim of the present investigation was to investigate if a correlation exists in these patients
Autor:
W J, Morgan, S M, Butler, C A, Johnson, A A, Colin, S C, FitzSimmons, D E, Geller, M W, Konstan, M J, Light, H R, Rabin, W E, Regelmann, D V, Schidlow, D C, Stokes, M E, Wohl, H, Kaplowitz, M M, Wyatt, S, Stryker
Publikováno v:
Pediatric pulmonology. 28(4)
Cystic fibrosis (CF) is a complex illness characterized by chronic lung infection leading to deterioration in function and respiratory failure in over 85% of patients. An understanding of the risk factors for that progression and the interaction of t
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 283(3)
Elastases in cystic fibrosis (CF) pulmonary fluids damage lung tissue and perpetuate cycles of infection, inflammation and injury. Elastases from three different sources may be present in CF airways: neutrophils, macrophages and Pseudomonas. We measu
Publikováno v:
American journal of respiratory and critical care medicine. 153(4 Pt 1)
In order to determine the long-term sequelae of prune belly syndrome (PBS) and whether the absence of abdominal wall musculature impairs exercise performance we studied nine patients 6 to 31 yr of age with PBS. Conventional spirometry, lung volumes,
Autor:
H J, Fuchs, D S, Borowitz, D H, Christiansen, E M, Morris, M L, Nash, B W, Ramsey, B J, Rosenstein, A L, Smith, M E, Wohl
Publikováno v:
The New England journal of medicine. 331(10)
Respiratory disease in patients with cystic fibrosis is characterized by airway obstruction caused by the accumulation of thick, purulent secretions, which results in recurrent, symptomatic exacerbations. The viscoelasticity of the secretions can be
Autor:
Henry J. Fuchs, Arnold L. Smith, Daniel V. Schidlow, Ivan R. Harwood, Jay D. Eisenberg, Henry L. Dorkin, Steven Shak, Robert W. Wilmott, M. E. Wohl, Susan J. Astley, Bonnie W. Ramsey, Moira L. Aitken, Andrew A. Colin, Laura J. Meyerson, Ronald L. Gibson, Wylie Burke
Publikováno v:
The American review of respiratory disease. 148(1)
Chronic endobronchial bacterial infection evokes purulent airway secretions in patients with CF. The viscoelastic properties of these secretions is primarily due to the presence of polymerized DNA from degenerating leukocytes. Recombinant human DNase
Publikováno v:
Musclenerve. 15(5)
We studied 27 Duchenne muscular dystrophy patients having spinal fusion for scoliosis. One patient died intraoperatively of cardiac arrest; all others have done well with no instances of malignant hyperthermia, postoperative ventilatory system depend