Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Douglas N. Homnick"'
Autor:
Michael J Light, Carol J Blaisdell, Douglas N. Homnick, Michael S. Schechter, Miles M. Weinberger
You'll turn here often for the latest AAP findings and recommenations; assessment and testing how-tos; proven therapeutic strategies; procedures, and techniques; home care and monitoring considerations; and much more. Powerful problem-solving featur
Publikováno v:
Journal of Applied Gerontology. 34:118-126
Equine assisted activities (hippotherapy and therapeutic riding) improve balance in patients with disabilities such as cerebral palsy, but have not been systematically studied in older adults, at risk of falls due to balance deficits. We conducted a
Autor:
Douglas N. Homnick, William I. Young, Violanda Grigorescu, John Schuen, Mary Kleyn, Steven J. Korzeniewski, Samya Z. Nasr, Amy Goldstein-Filbrun
Publikováno v:
Pediatric Pulmonology. 46:23-30
Summary. Michigan’s Newborn Screening (NBS) Program began statewide screening for cystic fibrosis (CF) in October 2007. Confirmatory sweat testing is performed in infants having initial immunoreactive trypsinogen concentrations � 99.8th percentil
Autor:
Douglas N. Homnick, Sandra R. DeJong
Publikováno v:
Clinical Pediatrics. 46:431-436
Parent surveys seem to provide sufficient information for asthma case selection. In this study, elementary school children were identified for an asthma education program through a screening questionnaire, followed by a comprehensive family survey. T
Publikováno v:
Journal of Aerosol Medicine. 20:45-49
Tenacious airway secretions are responsible for much of the lung damage in cystic fibrosis (CF). Label warnings on potential secondary effects of some antihistamines include possible drying or thickening of lower airway secretions, suggesting that th
Publikováno v:
Pediatric Pulmonology. 40:251-256
Appetite stimulants have been used to help overcome decreased appetite and malnutrition in children and adults with various chronic illnesses, including cystic fibrosis (CF). Stimulants have included megestrol acetate (MA), cyproheptadine hydrochlori
Publikováno v:
Chest. 125:1507-1511
Study objective To compare the PercussiveTech HF (PTHF) device (Vortran Medical Technology 1; Sacramento, CA) to standard manual chest physiotherapy (CPT) with respect to acute changes in pulmonary function, sputum production, and pulse oximetry in p
Publikováno v:
Chest. 114:993-997
Study objective A preliminary study comparing the efficacy and safety of the flutter device (Flutter) to standard, manual chest physiotherapy (CPT) in hospitalized cystic fibrosis (CF) patients undergoing an acute pulmonary exacerbation. Design Open
Publikováno v:
The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG. 17(1)
OBJECTIVES To assess the ability of an empiric once-daily dosing (ODD) tobramycin regimen to achieve desired serum concentrations in patients with cystic fibrosis (CF); to determine an optimal dosage regimen, using pharmacodynamic parameters; and to
Autor:
Carrie Langbo, John Schuen, Craig R. Adamski, Mary Kleyn, Douglas N. Homnick, Catherine Allan, Myrtha Gregoire-Bottex Md, Samya Z. Nasr, Ibrahim Abdulhamid, Erin P. Carmany
Publikováno v:
Pediatric pulmonology. 48(2)
Summary. Objective: A quality improvement (QI) strategy to improve the rate of genetic counseling (GC) services was initiated in cystic fibrosis (CF) care Center E in 2010. This statewide study was conducted to determine: (1) GC rates before and afte