[PDF] Top 20 Cystic fibrosis, are we missing in India?
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Cystic fibrosis, are we missing in India?
... patients in relation to knowledge about diagnosis and prognosis of CF patients, availability about diagnostic and management services of CF was administered to the pediatricians who participated in the ... See full document
5
Plasma sCD14 as a biomarker to predict pulmonary exacerbations in cystic fibrosis.
... increase in sCD14, CRP, MCP-1 and MPO levels when transitioning from a stable to exacerbation health state, some individual patients had no change or even a slight decrease in biomarker levels (Figure ... See full document
7
Pseudomonas aeruginosa diversification during infection development in cystic fibrosis lungs
... seen in Figure 3.6, differences in biofilm formation are significant when we compare the results of ATCC 39324 morphotypes with PA01 morphotypes ...morphotypes, in appendix II and III, ... See full document
108
Mechanisms of CFTR functional variants that impair regulated bicarbonate permeation and increase risk for pancreatitis but not for cystic fibrosis.
... activation, we developed structural models of CFTR and conducted dynamic ...CFTR are currently available, we built a homology model based on the structure of a bacterial ABC transporter (Sav1866) ... See full document
15
Variation in MSRA modifies risk of neonatal intestinal obstruction in cystic fibrosis.
... accumulation in the crypts and lumen along with goblet cell hyperplasia are characteristic findings in the small and large intestine of Cftr 2/2 mice ...cells are the primary source for mucus ... See full document
10
Diagnosis, Prognosis and Personalized Treatment of Cystic Fibrosis
... that, in CF, only a portion of the disease phenotypic variability can be explained by the functional defect caused by the different CFTR mutations – which is accentuated by the variability detected amongst ... See full document
90
Dysregulated proinflammatory and fibrogenic phenotype of fibroblasts in cystic fibrosis.
... Morbi-mortality in cystic fibrosis (CF) is mainly related to chronic lung infection and inflammation, uncontrolled tissue rearrangements and fibrosis, and yet the underlying mechanisms remain ... See full document
10
Microbiota present in cystic fibrosis lungs as revealed by whole genome sequencing.
... microbiota in cystic fibrosis lungs is crucial since chronic inflammation due to microorganisms leads to lung damage and ultimately, ...methods are biased towards certain microbial groups, and ... See full document
7
Genotype-phenotype correlation in cystic fibrosis patients bearing [H939R;H949L] allele
... They are thought to affect the expression of the phe- notype by modulating the effect of mutations: the combina- tion of two missense mutations on the same allele has been described clinically either to improve ... See full document
5
Culture-Independent Identification of Nontuberculous Mycobacteria in Cystic Fibrosis Respiratory Samples.
... improvement in NTM DNA sequence detection with use of the modified lysis protocol supports inadequate bacterial lysis as a contributing factor to the underrepresentation of NTM in culture-independent ... See full document
13
Correction of the ion transport defect in Cystic Fibrosis by small molecules
... applied in outcome measures for clinical trials have made this approach increasingly simpler and easier (Anton et ...Indeed, in the present study, sedation was used primarily to reduce anxiety and ensure ... See full document
180
Abordagem nutricional na Fibrose Quística em idade pediátrica.
... O íleo meconial é a condição gastrointestinal que surge mais precocemente, afetando 10 a 20% dos doentes no período neonatal (29, 31) . Esta resulta de uma produção, ainda in útero, de um mecónio hiperviscoso. A ... See full document
28
Surfactant protein a in cystic fibrosis: supratrimeric structure and pulmonary outcome.
... expected in CF patients neutrophils and elastase activity were elevated in CF BAL fluid (36638 U/ml, n = 18, compared to normal reference where there is no free elastolytic activity ...activity in ... See full document
7
Rev. LatinoAm. Enfermagem vol.22 número5
... 15. Kourrouski MFC, Abreu IS, Oliveira ACGM, Santos DMSS, Deon KC, Cervi MC, et al. Brazilian children and adolescents infected with HIV: the initial stage of development an instrument of health-related quality of life - ... See full document
7
J. bras. pneumol. vol.35 número2
... mortality. In an acute presentation, it can result in restriction of chest wall movement, retention of secretions, difficulty in performing adequate respiratory therapy, exacerbation of infection, ... See full document
3
Clinical significance in non-cystic fibrosis bronchiectasis followed in a real practice
... All patients underwent (RCT of the chest (iSpeed Advantage; General Electric Medical Systems, Milwaukee, W), USA . (igh-resolution images were obtained in full inspiration for all pa- tients, while expiratory ... See full document
10
Are we there yet?
... delineated in the Charter (advocating, enabling, and mediating) and recommended five action areas, which at the time of publication were awaited but also considered quite radical (Scriven and Speller ...opment ... See full document
7
Rev. esc. enferm. USP vol.45 número3 en v45n3a13
... A Fibrose Cística é uma doença crônica que grande impacto exerce sobre a vida familiar. A experiência da doença é a maneira pela qual os indivíduos respondem à doença, atri- buindo significados e buscando maneiras para ... See full document
7
Genotypic characterization of clinical isolates of Pseudomonas aeruginosa
... (“h”), in order to split the Pseudomonas aeruginosa collection into large genotypic groups to be studied jointly with the metadata ...selected in order not to have more than 25 genotypic groups to work ... See full document
116
Radiol Bras vol.48 número6
... Continuous motion from cardiac and vascular pulsation and respiratory motion are one of the major challenges in MRI of the chest as they severely affect imaging quality. A significant limita- tion of ... See full document
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