[PDF] Top 20 Análisis de algunas dificultades en el aprendizaje en un tema de álgebra en alumnos de primer año de la universidad
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PULMONARY MECHANICS IN ASTHMA AND CYSTIC FIBROSIS
... Maxinlum expiratory flow rates on flow- volume curves are often decreased below normal linmit.s in children with asthma or cystic fibrosis who are clini-.. cally vell and whose standard [r] ... See full document
97
Mucoactive drugs
... ABSTRACT: Mucus hypersecretion is a clinical feature of severe respiratory diseases such as asthma, cystic fibrosis and chronic obstructive pulmonary disease. Airway mucosal infection and/ or ... See full document
8
Unusual Clustering of Allergic Bronchopulmonary Aspergillosis in Children With Cystic Fibrosis
... Laufer P: Assessment of corticosteroid therapy for allergic bronchopulmonary aspergillosis in a patient with cystic fibrosis. J Asthma 1985;22:253-355[r] ... See full document
63
Inhaled protein/peptide-based therapies for respiratory disease
... obstructive pulmonary disease (COPD), and cystic fibrosis (CF) are all chronic pulmonary diseases, albeit with different etiologies, that are characterized by airflow limitation, chronic ... See full document
133
Pulmonary Aspergillosis: A Review on Diagnosis and Management
... a pulmonary disorder caused by hypersensitivity to Aspergillus fumigatus that complicates the course of patients with asthma and cystic ...refractory asthma, recurrent fleeting ... See full document
102
MCP-1/CCL2 in a Bulgarian cohort of children with
... childhood asthma; bronchial asthma; severe asthma; cystic fibrosis; chronic obstructive pulmonary 32.. disease.[r] ... See full document
8
Challenging the diagnosis of Cystic Fibrosis in a patient carrying the 186-8T/C allelic variant in the CF Transmembrane Conductance Regulator gene
... of pulmonary function and lung tissue destruction, but it can also be associated with suffi- cient residual pancreatic function and a much milder clin- ical picture ... See full document
12
Non ∆F 508 Cystic Fibrosis Diagnosed at Age 50 in an African American Male: A Primary Care Perspective
... The increasing number of atypical CF, which represents approximately 2% of affected patients [2], will make clinical diagnosis more challenging. Patients who are first diagnosed with CF as adults are more likely to have ... See full document
318
FAMILIAL FIBROCYSTIC PULMONARY DYSPLASIA AND ITS RELATION TO THE HAMMAN-RICH SYNDROME
... cases (Cases 90, 91 and 92) of congenital cystic disease of the lung with progressive pulmonary fibrosis.. Two of these occurred in brothers.[r] ... See full document
6
NonTuberculous Mycobacteria infection and lung transplantation in cystic fibrosis: a worldwide survey of clinical practice
... NTM pulmonary disease (NTM PD) involves clinical, radiological and microbiological criteria and is widely used clinically ...Importantly, pulmonary infection with ... See full document
5
Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosis
... Cystic fibrosis (CF) is a common autosomal recessive disease caused by mutations in the CF transmembrane conductance regulator gene. Recombinant adenoviruses have shown promise as vectors for transfer of CF ... See full document
87
Pathogenesis, imaging and clinical characteristics of CF and non-CF bronchiectasis
... severe asthma patients, Aspergillus fumigatus sensitization has also been associated with poorer lung function and an increased incidence of bronchiectasis, a likely cause and consequence for this anatomical ... See full document
112
A prospective pilot study of home monitoring in adults with cystic fibrosis (HOME CF) : protocol for a randomised controlled trial
... a pulmonary exacerbation. Pulmonary exacerbations are typically treated with antibi- otics targeted at the bacteria that cause chronic infection in that individual ...a pulmonary exacerbation ... See full document
9
EVALUATION OF JET-TYPE AND ULTRASONIC NEBULIZERS IN MIST TENT THERAPY FOR CYSTIC FIBROSIS
... “mist tent” therapy in the treatment of the ob- structive pulmonary lesion of cystic fibrosis and of the effectiveness of the ultrasonic nebuhizer, at least for the short-term treatment [r] ... See full document
131
Contrast-enhanced ultrasonography of the pancreas shows impaired perfusion in pancreas insufficient cystic fibrosis patients
... During a 4-year period (December 2010–May 2014), CF patients aged > 15 years attending regular follow up in the CF clinic were offered a detailed evaluation of the pancreas in this prospective observational study. The ... See full document
18
Management of refractory <em>Pseudomonas aeruginosa</em> infection in cystic fibrosis
... Abstract: Cystic fibrosis (CF) is the most common life-limiting inherited disease in Caucasian populations. The main cause of death in CF patients is respiratory failure resulting from chronic ... See full document
5
Clinical implications and characterization of Group A Streptoccoccus infections in adults with cystic fibrosis
... Keywords: Cystic fibrosis, Streptococcus pyogenes , Group A Streptococci, GAS, Pulmonary exacerbation, Eradication, Emerging pathogen.. * Correspondence: [email protected].[r] ... See full document
16
EARLY DETECTION OF PULMONARY FUNCTION ABNORMALITIES IN CYSTIC FIBROSIS
... lung volumes, flow rates and airway conductance, diffusing capacity and mixing efficiency were nor- mal... A significant decrease in arterial oxygen ten- sion was found together with a s[r] ... See full document
307
Intravenous antibiotics for pulmonary exacerbations in people with cystic fibrosis
... The authors aimed to only consider the first pulmonary exacerba- tion for each participant, taking the measure of effect as the dif- ference between baseline and the end of treatment. The optimal duration of ... See full document
112
Pulmonary Pseudomonas Colonization in Cystic Fibrosis
... Children Medical Center because of gastrointestinal and/or pulmonary disturbances, were enrolled in this study. Management began by taking a medical history, physical examination, sputum or pharyngeal swab for ... See full document
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