[PDF] Top 20 Inflammation and airway microbiota during cystic fibrosis pulmonary exacerbations.
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Inflammation and airway microbiota during cystic fibrosis pulmonary exacerbations.
... barcodes, and any sample where the control exhibited amplifica- tion by agarose gel electrophoresis underwent repeat PCR ...(annealing) and 60 s at 65 uC ...(Invitrogen) and mixed in equal volumes ... See full document
13
IP-10 is a potential biomarker of cystic fibrosis acute pulmonary exacerbations.
... in airway epithelial culture and the broad literature regarding the role of IP-10 in acute and chronic infection lend biological plausibility to the findings of our ...family, and is released ... See full document
10
Reduced nasal nitric oxide production in cystic fibrosis patients with elevated systemic inflammation markers.
... chronic inflammation in CF upper and lower airways, since NO is known to be increased during airway inflammation ...IL-1b and interferon-c [11], but until now, no coherence ... See full document
8
Changes in cystic fibrosis airway microbial community associated with a severe decline in lung function.
... the airway microbial community composition ...CF airway infections are polymicrobial [7] and that the microbiota, as a collective entity, may contribute to pathophysiologic processes ... See full document
19
Impact of the CFTR-potentiator ivacaftor on airway microbiota in cystic fibrosis patients carrying a G551D mutation.
... similarity and after normalization to the lowest number of reads for a sample (14,855 reads), 129 operational taxonomic units (OTUs) were identified, representing 64 ...core microbiota, representing OTUs ... See full document
18
J. bras. pneumol. vol.35 número2
... interfaces and two different pressure settings (for expiratory positive airway pressure—EPAP—and inspiratory positive airway pressure—IPAP— levels): low-pressure (EPAP of 6 cmH 2 O and ... See full document
3
J. bras. pneumol. vol.34 número2 en v34n2a04
... used and 30% when a more conserva- tive TRV cut-off point was ...patients and should be monitored during their follow-up ..., and FVC, than did the group classified as not having PH, which ... See full document
8
Pulmonary bacteriophage therapy on Pseudomonas aeruginosa cystic fibrosis strains: first steps towards treatment and prevention.
... earlier and followed their survival (Figure ...survival and the high dose (3610 8 pfu) was associated with a greater rate of survival than the low dose (3610 7 pfu) throughout the experiment (16 ... See full document
9
PDF EN Jornal Brasileiro de Pneumologia 2 4 english
... used and 30% when a more conserva- tive TRV cut-off point was ...patients and should be monitored during their follow-up ..., and FVC, than did the group classified as not having PH, which ... See full document
8
PDF EN Jornal Brasileiro de Pneumologia 2 8 english
... Objetivo: Avaliar a qualidade de vida (QV) de pacientes com fibrose cística (FC) acompanhados em um centro universitário de referência em atendimento a FC. Métodos: Estudo transversal com a aplicação do Cystic ... See full document
9
J. bras. pneumol. vol.40 número5
... Objective: To analyze the effects of Pilates mat exercises in patients with cystic fibrosis (CF). Methods: This was a clinical trial involving 19 CF patients recruited from either the CF Outpatient Clinic ... See full document
7
Pseudomonas aeruginosa diversification during infection development in cystic fibrosis lungs
... A Fibrose Quística (FQ) é uma doença genética que ocorre quando existe um defeito no cystic fibrosis conductance regulator gene (CFTR). Esta doença afeta vários órgãos, sendo as vias respiratórias as mais ... See full document
108
J. bras. pneumol. vol.37 número2 en v37n2a08
... with cystic fibrosis (CF) followed at a university referral center for ...the Cystic Fibrosis Questionnaire (CFQ) and Shwachman score in CF patients between April of 2008 and ... See full document
9
Rev. LatinoAm. Enfermagem vol.22 número5
... - Cystic Fibrosis Module (self version) for Brazilian children and ...girls and 59 boys; mean age ...Gerais and the Federal District, 51 of whom participated in the pilot study ... See full document
7
Structure and function of the cystic fibrosis transmembrane conductance regulator
... dehydration, and chronic Pseudomonas aeruginosa and Staphylococcus aureus lung infection, responsible for 90% of the mortality of CF ...1989 and its protein product CFTR is activated by an increase ... See full document
8
Rev. Nutr. vol.28 número4
... negatively and significantly associated with BMI and energy ...intake and, consequently, poorer nutritional status. Individuals with cystic fibrosis with good nutritional status also ... See full document
12
Diagnosis, Prognosis and Personalized Treatment of Cystic Fibrosis
... me and for saving me a position in your future lab (I will not forget ...advices and suggestions and for having a work ethic I ...teach and for having a hilarious twisted ...experience ... See full document
90
Design of pulmonary rehabilitation programmes during acute exacerbations of COPD : a systematic review and network meta-analysis
... more exacerbations, hospitalisations and death [1, ...events and prevent their recurrence [1]. Pulmonary rehabilitation is a comprehensive intervention presenting well-established benefits in ... See full document
13
Coincidence of Cystic Fibrosis in Mother and her Child Related to Infertility
... race and varies between different populations (from 1 / 2500– 1 ...U.S.A. and Canada, Cohen obtained information on 129 pregnancies in 100 patients with ...incidence and attests to the recessive ... See full document
3
Sao Paulo Med. J. vol.121 número5
... with cystic fibrosis who are not capable of expectorating, do not reliably predict the pres- ence of lower airway pathogens, lack sensitiv- ity for identifying Pseudomonas aeruginosa and ... See full document
7
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