[PDF] Top 20 STUDIES IN CYSTIC FIBROSIS
Has 10000 "STUDIES IN CYSTIC FIBROSIS" found on our website. Below are the top 20 most common "STUDIES IN CYSTIC FIBROSIS".
STUDIES IN CYSTIC FIBROSIS
... During this 20-year study period a num- ber of complications led to hospital admis- sion. Of 63 patients in Group A, 28 were admitted to the hospital for a total of 50 hos- pitalizations[r] ... See full document
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STUDIES IN CYSTIC FIBROSIS
... STUDIES IN CYSTIC FIBROSIS: A Report on Sixty-Five Patients over 17 Years of. Services[r] ... See full document
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STUDIES IN CYSTIC FIBROSIS: DETERMINATION OF SWEAT ELECTROLYTES IN SITU WITH DIRECT READING ELECTRODES
... ELECTROLYTES IN SITU WITH DIRECT READING ELECTRODES STUDIES IN CYSTIC FIBROSIS: DETERMINATION OF SWEAT. http://pediatrics.aappublications.org/content/43/5/794[r] ... See full document
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Micropuncture studies of the sweat formation in cystic fibrosis patients
... in cystic fibrosis, osmolality and concentrations of sodium and chloride were measured in fluid obtained by micropuncture from the sweat gland coil of the nail fold of patients with this ... See full document
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STUDIES IN THE PHYSIOLOGY OF SWEATING IN CYSTIC FIBROSIS
... Two types of experimental sweat gland fatigue with repeated injections of methacholine, and the observed frequencies in patients with cystic. fibrosis and in controls[r] ... See full document
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STUDIES ON THE LABORATORY DIAGNOSIS OF CYSTIC FIBROSIS OF THE PANCREAS
... A study of 78 patients with cystic fibrosis of the pancreas was carried out to determine whether gelatin-liquefying bacteria may be responsible for gelatin liquefaction of gelatin film b[r] ... See full document
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Cystic fibrosis and the relevance of the whole body vibration exercises in oscillating platforms: a short review
... The primary symptoms of the CF involve the lungs however an important increase in the life expectancy [2] has been noticed. In consequence, co-morbidities affect- ing organ systems other than the lungs have been re- ... See full document
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No benefit of longer eradication therapy of Pseudomonas aeruginosa primoinfections in pediatric cystic fibrosis
... Our analysis of secondary outcomes revealed no sig- nificant difference between groups in terms of age, as reported in a previous study [7]. Most of our patients were symptomatic at the time of the diagnosis. In a ... See full document
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Errors, Gaps, and Misconceptions in the Disease-Related Knowledge of Cystic Fibrosis Patients and Their Families
... Some studies report global knowledge to be satisfactory among cystic fibrosis patients and their parents, but these studies are based largely on impressions and have failed to examine sp[r] ... See full document
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Status of gene therapy for cystic fibrosis lung disease
... clinical studies that an order or two of magnitude increase in efficiency will be required for gene transfer to be therapeutically relevant in ...expression studies in the mouse nose (but not infec- tion ... See full document
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Mutation and Rare Polymorphisms Insight in Exons 7 and 20 of CFTR Gene in Non-Caucasian Cystic Fibrosis Patients
... heterozygous state. c.910C>T (R334W) mutation is a pathogenic mutation which causes the substitution of arginine to tryptophan amino acid in CFTR protein. Tryptophan is a relatively huge amino acid and if settles on a ... See full document
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Monitoring clinical and microbiological evolution of a cystic fibrosis patient over 26 years: experience of a Brazilian CF Centre
... have shown that CF patients chronically colonized with Bcc present greater deterioration of lung function, re- quire frequent antibiotic therapy and display increased mortality when compared to patients colonized with P. ... See full document
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Microbiological aspects of infection with Pseudomonas aeruginosa in patients with cystic fibrosis
... that studies designed to evaluate the efficacy of antibiotic therapy in CF are difficult to interpret because many agents are prescribed in varying doses and are given by different routes for varying lengths of ... See full document
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Identification and regulation of the cystic fibrosis transmembrane conductance regulator generated chloride channel
... regulation is due to phosphorylation, because the catalytic subunit of cAMP-dependent protein kinase plus ATP reversibly activated the channel in excised, cell-free patches of membrane. In symmetrical Cl- solutions, the ... See full document
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Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosis
... keys that received intrapulmonary adenovirus (21). In those studies, higher doses of vector (on a per-kilogram basis) were used, and the animals were seronegative before administration. Although not all of the ... See full document
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NonTuberculous Mycobacteria infection and lung transplantation in cystic fibrosis: a worldwide survey of clinical practice
... The incidence of respiratory cultures positive for NTM in people with CF has risen over recent decades [3]. Multicenter studies have reported varying prevalence that ranges from 2.7% across Europe [4], 6.6% in ... See full document
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Contrast-enhanced ultrasonography of the pancreas shows impaired perfusion in pancreas insufficient cystic fibrosis patients
... Presently, this is the only study describing perfusion aspects in the CF pancreas. The CF pancreas was chosen to evaluate the CEUS bolus-and-burst method due to the clear and homogenous discrimination between healthy and ... See full document
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THE ISLETS OF LANGERHANS IN PANCREATIC FIBROSIS
... FIG. Intravenous glucose tolerance test in normal child and in three patients with cystic fibrosis of the pancreas.. tobogic technique was used in these studies.[r] ... See full document
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A non-randomised single centre cohort study, comparing standard and modified bowel preparations, in adults with cystic fibrosis requiring colonoscopy
... with cystic fibrosis (CF) have been reported to be at five to ten-fold risk (25 to 30 fold risk after solid organ transplant) of colorectal cancer (CRC) than the general ... See full document
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DIAGNOSIS OF CYSTIC FIBROSIS OF THE PANCREAS
... toms and are the major problem of cystic fibrosis. These children with advanced forms of cystic fibrosis are literally stmffo- cated by these secretions. Figure 1 shows.. how copioums th[r] ... See full document
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