نتایج جستجو برای: cystic lung disease

تعداد نتایج: 1751468  

2017
Jesper Rømhild Davidsen Elisabeth Bendstrup Daniel P Henriksen Ole Graumann Christian B Laursen

Background: Lung ultrasound (LUS) used to identify interstitial syndrome (IS) and pleural thickening related to diffuse parenchymal lung disease (DPLD) has shown significant correlations with ground glass opacity (GGO) on high-resolution computed tomography (HRCT). However, the applicability of LUS in patients with DPLD subtypes as rare cystic lung diseases has not previously been investigated....

2016
Renan Marrichi Mauch Arthur Henrique Pezzo Kmit Fernando Augusto de Lima Marson Carlos Emilio Levy Antonio de Azevedo Barros-Filho José Dirceu Ribeiro

OBJECTIVE To review the literature addressing the relationship of growth and nutritional parameters with pulmonary function in pediatric patients with cystic fibrosis. DATA SOURCE A collection of articles published in the last 15 years in English, Portuguese and Spanish was made by research in electronic databases - PubMed, Cochrane, Medline, Lilacs and Scielo - using the keywords cystic fibr...

Journal: :Proceedings of the Royal Society of Medicine 1939

Journal: :Allergy, Asthma & Respiratory Disease 2020

Journal: :Respiratory Medicine Case Reports 2019

Journal: :New England Journal of Medicine 2015

Journal: :Proceedings of the Royal Society of Medicine 1976

Journal: :The Lancet Respiratory Medicine 2020

Journal: :American journal of physiology. Lung cellular and molecular physiology 2008
Christopher S Rogers William M Abraham Kim A Brogden John F Engelhardt John T Fisher Paul B McCray Geoffrey McLennan David K Meyerholz Eman Namati Lynda S Ostedgaard Randall S Prather Juan R Sabater David Anthony Stoltz Joseph Zabner Michael J Welsh

Airway disease currently causes most of the morbidity and mortality in patients with cystic fibrosis (CF). However, understanding the pathogenesis of CF lung disease and developing novel therapeutic strategies have been hampered by the limitations of current models. Although the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) has been targeted in mice, CF mice fail ...

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