[PDF] Top 20 IP-10 is a potential biomarker of cystic fibrosis acute pulmonary exacerbations.
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IP-10 is a potential biomarker of cystic fibrosis acute pulmonary exacerbations.
... (NLF) is readily obtained biologic fluid that has been previously used to monitor inflammation of the upper airway, and may also reflect disease activity in the CF lung ...characterization of airway ... See full document
10
Metabolomics of pulmonary exacerbations reveals the personalized nature of cystic fibrosis disease
... chemistry of sputum samples compared in this study was more similar within patients through time than across patients with the same clinical ...signature of exacerbation, personalized approaches to ... See full document
21
Inflammation and airway microbiota during cystic fibrosis pulmonary exacerbations.
... marker of response to ...as potential pathogens ...question of whether or not Prevotella is a pathogen in CF; however, the number of patients in our study was small and the majority ... See full document
13
Plasma sCD14 as a biomarker to predict pulmonary exacerbations in cystic fibrosis.
... review. Exacerbations during the follow-up period were ascertained through chart review (up to 2 years following enrollment) by study personnel blinded to the biomarker ...follow-up exacerbations ... See full document
7
The microbial community of the cystic fibrosis airway is disrupted in early life.
... one of the comparison groups ...Both of these eOTUs were significantly less abundant in the CF ...procedure is a harsh method for adjusting for multiple testing therefore a permutation test was ... See full document
19
Sao Paulo Med. J. vol.121 número5
... ease of infants and children, although adult cases are being recognized with greater fre- ...There is no sex predominance. In- volvement of the lungs usually is manifested clinically by ... See full document
7
Rev. Nutr. vol.28 número4
... model of Poisson regression, it could be seen that the presence of delta F508 mutation was negatively and significantly associated with BMI and energy ...with cystic fibrosis with good ... See full document
12
Braz. j. . vol.83 número6
... Methods: Clinical symptoms (pulmonary, pancreatic insufficiency, malnutrition, nasal obstruc- tion), two positive sweat chloride tests, and genotype findings in 23 patients with cystic fibrosis were ... See full document
6
Serum MicroRNAs as Potential Biomarkers for Early Diagnosis of Hepatitis C Virus-Related Hepatocellular Carcinoma in Egyptian Patients.
... liver fibrosis and hepatocellular carcinoma (HCC) and are candidate ...the potential of serum microRNAs; miR-19a, miR-296, miR-130a, miR-195, miR-192, miR-34a, and miR-146a as early diagnos- tic ... See full document
23
Coincidence of Cystic Fibrosis in Mother and her Child Related to Infertility
... diagnosis of ei- ther asthma, chronic bronchitis, or ...insufficiency is much less common in adults diagnosed with CF, but pancreatitis occurs with greater ...disease is generally less severe in CF ... See full document
3
HMGB1 Is a Potential Biomarker for Severe Viral Hemorrhagic Fevers.
... members of the Bunyaviridae family, represent important causative agents of ...hantavirus is closely related to a specific rodent or insectivore natural ...HFRS is an endemic disease in ... See full document
10
J. bras. pneumol. vol.35 número1 en v35n1a06
... use of inhaled albuterol modifies the pulmonary deposition of inhaled tobramycin in patients with cystic fibrosis (CF) and whether pulmonary deposition correlates with disease ... See full document
9
Design of pulmonary rehabilitation programmes during acute exacerbations of COPD : a systematic review and network meta-analysis
... more exacerbations, hospitalisations and death [1, ...impact of these events and prevent their recurrence [1]. Pulmonary rehabilitation is a comprehensive intervention presenting ... See full document
13
J. Pediatr. (Rio J.) vol.84 número5 en v84n5a05
... review of PFT and the clinical records of children over 5 years of age attending the RCCH CF Clinic, situ- ated in the Western Cape Province of South Africa, from Janu- ary 1999 to December ... See full document
7
J. bras. pneumol. vol.32 número6 en a06v32n6
... there is a positive correlation with the radiological aspects and clinical ...number of cases, difficulties arise due to the superimposition of morphological patterns and the low representativeness ... See full document
5
Calcium-activated chloride in cystic fibrosis
... protein is clearly membrane localized when expressed in baby hamster ovary (BHK) cells, as demonstrated by lack of fluorescence labelling of a putative extracellularly accessible Flag-tag (Figure ... See full document
160
Arq. Bras. Cardiol. vol.92 número4 en v92n4a14
... arterial pulmonary hypertension is an incurable disease, of which mean time of survival after the diagnosis is approximately two years and a half, according to the National Institutes ... See full document
8
Dyspnea perception in cystic fibrosis patients
... proportion of cases, means±SD, or median (interquartile ...comparison of repeated measurements between CF patients and normal subjects during inspiratory resistive load ...completion of the dyspnea ... See full document
7
Is ‘msonge’ a house? Visualizing a novel in the L2 classroom: The case of Swahili
... Dwelling is one of the basic human needs and therefore it is found in all societies, but in various ...dwelling is among the basic needs of humans because it provides shelter against ... See full document
15
Pulmonary bacteriophage therapy on Pseudomonas aeruginosa cystic fibrosis strains: first steps towards treatment and prevention.
... doses of P3-CHA bacteriophage intranasally (mimicking a nebulisation treatment for humans) to two groups of mice that had received a lethal dose of the CHA strain 2 h earlier and followed their ... See full document
9
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