A5072369910- Cystic Fibrosis Research Advances
- Tracheal and airway disorders
- Chronic Obstructive Pulmonary Disease (COPD) Research
- Neonatal Respiratory Health Research
- Respiratory Support and Mechanisms
- Obstructive Sleep Apnea Research
- Neuroscience of respiration and sleep
- Antifungal resistance and susceptibility
- Inhalation and Respiratory Drug Delivery
- Asthma and respiratory diseases
- Nematode management and characterization studies
- Pneumonia and Respiratory Infections
- Dysphagia Assessment and Management
- Pleural and Pulmonary Diseases
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Pulmonary Hypertension Research and Treatments
- Neurological disorders and treatments
- Innovations in Medical Education
- Child Nutrition and Feeding Issues
- Congenital Heart Disease Studies
- Immunodeficiency and Autoimmune Disorders
- Aging, Health, and Disability
- Cardiovascular and Diving-Related Complications
- Oral and gingival health research
- Nursing Diagnosis and Documentation
Centro de Investigación Biomédica en Red de Enfermedades Respiratorias
2016-2025
Instituto de Biomedicina de Sevilla
2016-2025
Hospital Universitario Virgen del Rocío
2016-2025
Instituto de Salud Carlos III
2015-2025
Universidad de Sevilla
2011-2025
Hospital Universitario de La Princesa
2022-2023
Hospital Universitario La Paz
2018
Consejo Superior de Investigaciones Científicas
2014-2015
Unidades Centrales Científico-Técnicas
2014
Hospital San Borja Arriarán
2004
The present study assessed the usefulness of home cardiorespiratory polygraphy as an alternative to overnight polysomnography for diagnosis sleep-disordered breathing in heart failure. A total 75 patients with chronic stable failure due systolic dysfunction (left ventricular ejection fraction ≤45%) underwent at Virgen del Rocio Hospital and home. two studies were performed random order within 30 days. accuracy polygraphical findings was determined by sensitivity specificity obtained area...
Cystic fibrosis transmembrane conductance regulator (CFTR) is expressed in human skeletal muscle cells. Variations of CFTR dysfunction among patients with cystic may be an important determinant maximal exercise capacity fibrosis. Previous studies on the relationship between genotype and are scarce contradictory.This study was designed to explore factors influencing capacity, as peak oxygen uptake (V.O2peak), a specific focus children adults fibrosis.In international, multicenter,...
Knowing the cost of hospitalizations for exacerbation in bronchiectasis patients is essential to perform cost-effectiveness studies treatments that aim reduce exacerbations these patients.To find out mean due patients, and identify factors associated with higher costs.Prospective, observational, multicenter study adult hospitalized exacerbation. All expenses from patients' arrival at hospital their discharge were calculated: diagnostic tests, treatments, transferals, home hospitalization,...
Summary Objective To date, available mortality trends due to cystic fibrosis (CF) have been limited the analysis of certain countries in different parts world showing that constantly decreasing. However, no studies examined Europe as a whole. The present study aims analyze CF by gender within European Union (EU) and quantify potential years life lost (PYLL). Design Deaths from 27 EU were obtained statistical office 1994–2010. Crude age‐standardized rates (ASR) estimated for women men using...
Nutritional status and daily physical activity (PA) may be an excellent tool for the maintenance of bone health in patients with cystic fibrosis (CF).To evaluate relationship between nutritional status, turnover patients.A cross-sectional study adolescent adult diagnosed clinically stable was conducted. Total body, femoral neck, lumbar spine mineral density (BMD) were determined by dual energy X-ray absorptiometry metabolism markers ALP, P1NP, PICP, ß-CrossLaps. PA monitoring assessed 5...