Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alois Zapletal"'
Autor:
J. Chalupová, Alois Zapletal
Publikováno v:
Pediatric Pulmonology. 33:174-180
Rhinomanometry allows objective assessment of nasal patency in pediatric patients with nasal and other respiratory problems. However, no reliable reference values are available in the pediatric age group. We measured nasal inspiratory airflow and nas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11acfa7b50220f0c83e45449f3b25b10
https://doi.org/10.1002/ppul.10066
https://doi.org/10.1002/ppul.10066
Autor:
Alois Zapletal, Peter Greally, Blakeslee E. Noyes, Steven R. Boas, John M. Armitage, Geoffrey Kurland, David M. Orenstein, Albert Faro
Publikováno v:
Pediatric Pulmonology. 23:87-94
Maximum expiratory and inspiratory flow-volume (MEFV, MIFV) curves, specific airway conductance (sGaw), and flexible fiberoptic laryngoscopy were examined in 8 pediatric lung transplant recipients with vocal cord paralysis (VCP). Six were heart-lung
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f16a23821c73ec72e1ff93c16a59823c
https://doi.org/10.1002/(sici)1099-0496(199702)23:2<87::aid-ppul3>3.0.co
https://doi.org/10.1002/(sici)1099-0496(199702)23:2<87::aid-ppul3>3.0.co
Publikováno v:
Respiration; international review of thoracic diseases. 75(1)
Background: The most frequently used parameters for assessing bronchoconstriction and bronchodilation are forced expiratory volume in 1 s (FEV1) and peak expiratory flow (PEF). Objectives: To assess the sensitivity of other parameters after induced b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3eb7e88dd8ed1ae5a6e9203476f2d1f2
https://pubmed.ncbi.nlm.nih.gov/17299253
https://pubmed.ncbi.nlm.nih.gov/17299253
Autor:
Otto Lochmann, Ivana Sekyrova, Milan MacekJr, Věra Vávrová, Zdenka Jedličková, Antonin Kolek, Milan Macek, Lenka Ťoukálková, Helena Honomichlová, Jiří Biolek, Dana Zemkova, Miroslava Šuláková, Hubert Vaníček, Hana Krásničanová, Alois Zapletal, Alena Holčíková, Jaromir Musil
Publikováno v:
Cystic Fibrosis Pulmonary Infections: Lessons from Around the World ISBN: 9783034873611
Since 1985, a total of 384 CF patients have been treated in the Czech Republic. Seventy five percent of patients have been treated in Prague, where a research center is also located, and 25% have been managed in other university and large regional ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::949de99119b594819420cfdbe68f9ae6
https://doi.org/10.1007/978-3-0348-7359-8_21
https://doi.org/10.1007/978-3-0348-7359-8_21
Publikováno v:
Pediatric pulmonology. 15(1)
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 22 children and young adults (8 with cystic fibrosis, 8 with asymptomatic asthma, and 6 he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2695ade7c0ac506f2170a0199a4ffdb
https://pubmed.ncbi.nlm.nih.gov/8419893
https://pubmed.ncbi.nlm.nih.gov/8419893
Publikováno v:
Quality of Life after Open Heart Surgery ISBN: 9789401051668
There are many reasons for an impairment of lung function in patients with congenital cardiac malformation. Cardiomegaly and distended pulmonary arteries occupy a space at the expense of the developing lung [1]. As early as 1887, von Basch found that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb56e16541ab0dc03cfd4169e703c41c
https://doi.org/10.1007/978-94-011-2640-3_29
https://doi.org/10.1007/978-94-011-2640-3_29
Publikováno v:
Pediatric Pulmonology. 1:154-166
Lung function of 65 patients who had idiopathic interstitial pulmonary fibrosis (IIPF) that had been treated with prednisone was evaluated by tests of ventilatory function, lung mechanics, and gas exchange at rest and during exercise. Ages on initial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa86f86439bd28ff49eabd510acdd595
https://doi.org/10.1002/ppul.1950010307
https://doi.org/10.1002/ppul.1950010307
Publikováno v:
Pediatrics. 48:64-72
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 and whose standard spirometric tests are within normal limits. In particular, maximum flow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::195c082a85548cb84096a838f601a4d7
https://doi.org/10.1542/peds.48.1.64
https://doi.org/10.1542/peds.48.1.64