Cystic fibrosis - Treatment.
Exercise is medicine for cystic fibrosis
... with Cystic Fibrosis, exercise is able to achieve in the long term, adaptations and changes in such important or- gans as the lungs, heart, bones and muscle tissue, strengthe- ning them and keeping them in ...
116
TítuloEradication of pseudomonas aeruginosa with inhaled colistin in adults with non cystic fibrosis bronchiectasis
... Comparison of exacerbations between pre- and post-treatment with inhaled colistin found a signifi- cant reduction in the number of exacerbations during the year with treatment. We observed significantly ...
9
Individual Patterns of Complexity in Cystic Fibrosis Lung Microbiota, Including Predator Bacteria, over a 1-Year Period
... antibiotic treatment, although other factors, such as the host’s immune system, human metabolites, bacterial quorum-sensing molecules, the spread of bacteriophages among bacteria, and other ecological forces, are ...
12
Anion transport mechanism of a triazole bearing derivative of prodigiosine: a candidate for cystic fibrosis therapy
... Cystic fibrosis (CF) is a genetic lethal disease, originated from the defective function of the CFTR protein, a chloride and bicarbonate permeable transmembrane ...the treatment of CF using ...
13
canales de cloro como blancos de drogas
... Insights emerging from basic research indicate broad opportunities and challenges for chloridechannelbased therapies. Compounds under development offer promise for the treatment of cystic fibrosis, ...
19
JOINT VENTURE PHILANTHROPY pdf
... (Cystic Fibrosis transmembrane Conductance Regulator), a protein complex that regulates the opening of the chloride channels of the cells lining the secretory ...with Cystic Fibrosis, ...
5
Fibrosis quistica
... The cystic fibrosis is an autosomic recessive disease, caused by a mutation localized in chromosome 7, distinguished by lesions in gastrointestinal tract and pulmonary ...difficult treatment (ie ...
6
Optimización de sondas en autómatas moleculares para el diagnóstico y tratamiento de la fibrosis quísticaProbe optimization in molecular automaton for diagnostic and treatment of cystic fibrosis
... and treatment of diseases at molecular ...the cystic fibrosis ∆F 508 gene mutation is studied, and thus a theoretical mechanism for diagnosis and treatment of such disease is ...
146
Clonal epidemiology and antimicrobial resistance in Pseudomonas aeruginosa chronic respiratory infections: interpatient transmission and resistome evolution of an international cystic fibrosis clone
... More worrisome, when investigating long-term clonal epidemiology of P. aeruginosa colonizing the respiratory tract of CF patients from the Balearic Islands, a clonal replacement of a MDR mutator strain by the MDR LES ...
320
Polymeric chemosensor for the detection and quantification of chloride in human sweat Application to the diagnosis of cystic fibrosis
... At present, there is no cure for CF and the pharmaceutical industry is making an intense effort to develop drugs for the treatment of this disease. There are two medicines currently approved, ivacaftor and ...
10
The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function
... of treatment with 100 mM glibenclamide or 5 mM ...of treatment with 100 mM glibenclamide or 5 mM ...of treatment with 5 mM GlyH101 or 5 mM CFTR(inh)-172, and WB of the mCx-III subunit UQCRC1, as ...
12
Manejo de rinosinusitis crnica en nios
... Chronic rhinosinusitis (CRS) in children and adults appear to have different etiology and therefore different diagnostic and treatment strategies. Adult chronic rhinosinusitis has a relatively greater inflammatory ...
9
Mortality prediction of cirrhotic patients admitted to the Intensive Care Unit
... prior treatment with IFN or IFN/RBV ...prior treatment at least 6 months before ...mild fibrosis defined as Metavir score 0-2 (equivalent to Ishak 0-3), and patients in Group B had severe ...
6
Development of a method to detect three frequent mutations in the CFTR gene using allele-specific real time PCR
... La fibrosis quística (FQ) es una enfermedad autosómica recesiva provocada por mutaciones en el gen regulador de la conductancia transmembranal de la fibrosis quística ...
6
Vol. 89, Núm. 5 (2018)
... Introduction: Cystic fibrosis (CF) is an inherited, progressive, multisystem disease. Better physical capacity may slow disease progression, thus improving prognosis and survival. The objective of this ...
6
Serum phospholipid fatty acid profile and dietary intake in an adult Mediterranean population with cystic fibrosis.
... the Cystic Fibrosis Foundation (CFF) consensus statement (Cystic Fibrosis Foundation, 1997), and who were being periodically followed up at the Adult Cystic Fibrosis Unit, Carlos ...
8
Detection of mutations in Cuban cystic fibrosis patients Teresa Collazo , Yaixa Piloto , Yulia Clark , Ana M Bofill , Manuel Gmez , Yadira Hernndez
... of cystic fibrosis is based on the presence of a multisystemic clinical symptomatology compatible with the disorder, together with two or more assays for electrolytes in sweat ...
5
Vol. 89, Núm. 3 (2018)
... 14 cystic fibrosis patients, our data indicate that the interpretation of functional respi- ratory involvement varies according to the theoreti- cal values used, diagnosing greater involvement with ...
7
Descargar Descargar PDF
... Mucinous cystic neoplasms of the mesentery are rare, have a lack of specific cli- nical findings, and are usually diagnosed incidentally as other mesenteric ...
5
Vol. 89, Núm. 2 (2018)
... of cystic pulmonary masses should consider both congenital airway mal- formation (cystic adenomatoid malformation) and type I ...include cystic lesions (especially peripheral) without clear etiology, ...
5
