Cystic fibrosis
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 ...
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TítuloEradication of pseudomonas aeruginosa with inhaled colistin in adults with non cystic fibrosis bronchiectasis
... non-cystic fibrosis bronchiectasis (NCFB) patients is associated with a worsening of the symptoms, increase of exacerbations, poor quality of life and functional ...
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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 ...
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The expression of the mitochondrial encoded gene ND4 is downregulated in cystic fibrosis
... Cystic fibrosis (CF) is a disease produced by mutations in the CFTR channel. We have previously reported that the CFTR chloride transport activity regulates the differential expression of several genes, ...
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Serum phospholipid fatty acid profile and dietary intake in an adult Mediterranean population with cystic fibrosis.
... with cystic fibrosis (CF) often have abnormal levels of essential fatty acid (EFA) in serum, plasma and blood cell membranes, as well as in tissue biopsies (Chris- tophe & Robberecht, 2001; Freedman et ...
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The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function
... Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the CFTR (Cystic Fibrosis Transmembrane Conduc- tance Regulator) ...
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Cystic Fibrosis: an overview of its basic aspects
... the cystic fibrosis transmembrane conductance regulator (CFTR) allows a better understanding of the pathology of this disease and the complex genotype – phenotype ...
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Polymeric chemosensor for the detection and quantification of chloride in human sweat Application to the diagnosis of cystic fibrosis
... We have developed a new extremely hydrophilic polymeric film suitable for the detection and quantification of chloride in human sweat directly on the skin. The film, or membrane, has chemically anchored ...
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Genetic Variation and Clinical Heterogeneity in Cystic Fibrosis
... Effect of CFTR gene mutations on the cystic fibrosis transmembrane conductance regulator (CFTR) protein and function. (Top) The CFTR gene with examples of each of the mutation classes and their positions in the ...
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JOINT VENTURE PHILANTHROPY pdf
... The most common mutations (F508) lead to a failure in the intracellular processing of the CFTR precursor and/or its expression on the cell membrane. This mutation affects two out of three patients with cystic ...
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canales de cloro como blancos de drogas
... the cystic fibrosis lung is reduced secretion of chloride, bicarbonate and fluid by airway submu cosal glands, resulting in a viscous, acidic airway surface liquid (ASl) that promotes bacterial ...
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Patrones de prescripción de antimicrobianos en pacientes españoles con fibrosis quística: resultados de un estudio multicéntrico nacional
... all cystic fibrosis Spanish pa- tients that agreed to participate in this multicenter ...en Fibrosis Quística): Amparó Solé and Isidoro Cortell (Hospital Universitario y Politécnico la Fe, Valencia, ...
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Vol. 89, Núm. 3 (2018)
... with Cystic Fibrosis and pancreatic insufficiency: Results of a systematic review: clinical practice guidelines on growth and nutrition subcommittee; ad hoc working ...
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Diferencias en la respuesta fisiológica durante la prueba de marcha 6 minutos y el test Glittre-ADL en pacientes con fibrosis quística: Estudio piloto
... 7. Fidika A, Herle M, Goldbeck H. Symptoms of depression affect the course of lung function in adolescents and adults with cystic fibrosis. Pulm Med. 2014; 14: 205. 8. Hagströmer M, Bergman P, De ...
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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 ...
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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 ...
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Validez y efectividad del programa de cribado neonatal de la fibrosis quística en Castilla y León. Período 1999-2014
... 29. Green A, Isherwood D, Pollitt R. A laboratory Guide to Newborn Screening n the UK for cystic fibrosis. London: UK National Screening Committe; 2009. Disponible en: www.newbloodspot.screening.nhs.uk . ...
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El nivel de ingresos bajos es un factor de riesgo importante en pacientes con fibrosis qustica del noreste de Mxico
... Association of Cystic Fibrosis (AMFQ, http:// www.fibrosisquistica.org. mx) had registered only 1,200 CF cases in 25 years; this means that about 15% of them are diagnosed, six thousand of Mexican CF ...
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Protocolo de seguimiento de pacientes con fibrosis quística diagnosticados por cribado neonatal
... c) Si no se encuentran mutaciones y la prueba del sudor es normal, estos serían los falsos positivos del programa. Otro grupo es el de aquellos neonatos en los que no se llega a alcanzar un diagnóstico concluyente, ni ...
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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
... Biomolecular computing is an interdisciplinary field whose purpose is to build mo- lecular devices based on concentrations of organic molecules, which at an external sti- mulus they self-assemble and organize in a ...
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