[PDF] Top 20 Hemoglobin oxygen affinity in patients with cystic fibrosis.
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Hemoglobin oxygen affinity in patients with cystic fibrosis.
... our patients iron metabolism was routinely checked and deficiency was ...[Hb] in other studies might be the counteracting effects between iron deficiency and hypoxia ...[erythropoietin] with FVC and ... See full document
10
The effects of 2,3-diphosphoglycerate, adenosine triphosphate, and glycosylated hemoglobin on the hemoglobin-oxygen affinity of diabetic patients
... combined with hyperventilation-in- duced alkalosis shifts the ODC to the ...of oxygen due to congenital cardiac problems, anemia and chronically reduced cardiac ...increase with a con- sequent ... See full document
7
J. bras. pneumol. vol.34 número2 en v34n2a04
... (PH) in patients with cystic fibrosis (CF), to compare clinical characteristics, radiographic scores, pulmonary function, and echocardiographic parameters in patients ... See full document
8
PDF EN Jornal Brasileiro de Pneumologia 2 4 english
... (PH) in patients with cystic fibrosis (CF), to compare clinical characteristics, radiographic scores, pulmonary function, and echocardiographic parameters in patients ... See full document
8
A first-year dornase alfa treatment impact on clinical parameters of patients with cystic fibrosis: the Brazilian cystic fibrosis multicenter study
... reduction in the number of emergency room visits in the six to 11 years ...changes in forced expiratory volume in one second (VEF 1 ), in forced vital capacity (FVC), in ... See full document
11
Dyspnea perception in cystic fibrosis patients
... 6MWT in a group of 25 adult CF patients with mild and moderate lung disease and in 22 healthy ...volunteers. In contrast to our research, CF patients walked similar distances but ... See full document
7
Rev. Assoc. Med. Bras. vol.60 número3
... patient in isolation and taking into consideration that the FEF 25-75% is the parameter that causes most ear- ly changes in CF, it was verified that 11 of the 23 patients studied presented an FEF ... See full document
6
Cytogenetics, JAK2 and MPL mutations in polycythemia vera, primary myelofibrosis and essential thrombocythemia
... DNA in a final volume of 50 ...seconds, with a final extension of 72°C for 7 ...stained with ethidium ...purified with the QIAquick PCR Purification kit (Qiagen) according to the ... See full document
8
J. bras. pneumol. vol.35 número2
... treated with a 20-gauge Seldinger-type intercostal chest drain, whereas the left pneumothorax was only ...treated with antibiotics (meropenem, 1 g tid; and colistin, 2 million units tid), bronchodilators ... See full document
3
Genotype-phenotype correlation in cystic fibrosis patients bearing [H939R;H949L] allele
... Caucasian patients [140 male, 149 female, median age 16 years, (range 1-46)], who attended since 1996 our CF Center at the Paediatric Department of the University of Bari, were ...mutations in trans ... See full document
5
Mechanisms of CFTR functional variants that impair regulated bicarbonate permeation and increase risk for pancreatitis but not for cystic fibrosis.
... agree in general with the CFTR model built by Norimatsu and collaborators [37,38] which was also confirmed by cysteine scanning experiments ...curve, with the gray band displaying the fluctuations ... See full document
15
PDF EN Jornal Brasileiro de Pneumologia 5 6 english
... used in order to compare pulmonary function tests with ...performed in order to determine which variables most influenced the Shwachman- Kulczycki total ... See full document
8
PDF EN Jornal Brasileiro de Pneumologia 2 7 english
... maneuver in order to provide clarification and familiarize the patients with ...PEF, in ten random respiratory ...20%. In situations in which the coefficient of variation was ... See full document
6
J. bras. pneumol. vol.38 número2 en v38n2a07
... resistance with the interrupter resistance (Rint) technique in patients with cystic fibrosis (CF) and to determine whether Rint values correlate with spirometric ... See full document
6
J. bras. pneumol. vol.34 número5 en v34n5a06
... 38 patients was needed in order to estimate correlations equal to or greater than ...0.50 with a level of signifi- cance of α = ...1), in a blinded fashion, by a pediatric radiologist of ... See full document
8
Braz. j. . vol.83 número6
... diagnosed with NP underwent treatment with nasal topic corticosteroid for six months, and were reeval- uated by endoscopy after this ...period. In case of persistent Polyposis, patients were ... See full document
6
Multidrug-Resistant Nontuberculous Mycobacteria Isolated from Cystic Fibrosis Patients
... CF patients as developed by Pas- choal et ...prevalent in distinct countries, reinforcing the im- portance of species identification in therapeutic decision ...CF patients may show resistance ... See full document
8
T helper cell subsets specific for Pseudomonas aeruginosa in healthy individuals and patients with cystic fibrosis.
... was with phycoerythrin-labelled anti-CD4 (RPA-T4; eBioscience), phycoerythrin-labelled anti-abTCR (IP26; eBioscience), phycoerythrin-Cy7-labelled anti-CCR4 (IGI; BD Pharminogen), AlexFluorH647-labelled anti-CCR9 ... See full document
10
Calcium-activated chloride in cystic fibrosis
... 1, in freshly isolated nasal cells from F508del-homozygous CF patients and non-CF healthy ...channels in cell lines stably expressing wild type (wt) or F508del-CFTR. In both cases no increase ... See full document
160
Effect of meconium ileus on the clinical prognosis of patients with cystic fibrosis
... difference in the survival of patients with cystic fibrosis (CF) with and without meconium ...127 patients with CF, whose diagnosis was confirmed by typical ... See full document
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