Search Results - "Zapletal, Alois"

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  1. 1

    Area under the maximum expiratory flow-volume curve--a sensitive parameter in the evaluation of airway patency by Zapletal, Alois, Hladíková, Marie, Chalupová, Jana, Svobodová, Tamara, Vávrová, Véra

    Published in Respiration (2008)
    “…The most frequently used parameters for assessing bronchoconstriction and bronchodilation are forced expiratory volume in 1 s (FEV(1)) and peak expiratory flow…”
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    Journal Article
  2. 2

    Lung function in children and adolescents with tetralogy of Fallot after intracardiac repair by Zapletal, A, Samanek, M, Hruda, J, Hucin, B

    Published in Pediatric pulmonology (01-07-1993)
    “…We studied lung function in 41 patients, aged 6-27 years, 1-5 years after intracardiac surgical repair (ICR) of tetralogy of Fallot (TOF) and about 5 years…”
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    Journal Article
  3. 3

    Lung recoil and the determination of airflow limitation in cystic fibrosis and asthma by Zapletal, A, Desmond, K J, Demizio, D, Coates, A L

    Published in Pediatric pulmonology (01-01-1993)
    “…A reduction of lung recoil pressure could aggravate any airflow limitation that might be present in patients with cystic fibrosis (CF) or asthma. In a group of…”
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    Journal Article
  4. 4

    Airway function tests and vocal cord paralysis in lung transplant recipients by Zapletal, Alois, Kurland, Geoffrey, Boas, Steven R., Noyes, Blakeslee E., Greally, Peter, Faro, Albert, Armitage, John M., Orenstein, David M.

    Published in Pediatric pulmonology (01-02-1997)
    “…Maximum expiratory and inspiratory flow‐volume (MEFV, MIFV) curves, specific airway conductance (sGaw), and flexible fiberoptic laryngoscopy were examined in 8…”
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    Journal Article Conference Proceeding
  5. 5

    Pulmonary mechanics in asthma and cystic fibrosis by Zapletal, A, Motoyama, E K, Gibson, L E, Bouhuys, A

    Published in Pediatrics (Evanston) (01-07-1971)
    “…Maximum expiratory flow rates on flow-volume curves are often decreased below normal limits in children with asthma or cystic fibrosis who are clinically well…”
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    Journal Article