Cystic fibrosis (CF)
Top PDF Cystic fibrosis (CF):
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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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) ...to CF. Burton L. Shapiro and ...
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The expression of the mitochondrial encoded gene ND4 is downregulated in cystic fibrosis
... Cystic fibrosis is the most common and lethal autosomic recessive disease among Caucasians [1, ...in CF, and characterized one as SRC, which encodes for the protein-tyrosine kinase c-Src ...a ...
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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 ...channel. CF mutations affect ...
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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; ...
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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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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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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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Genetic Variation and Clinical Heterogeneity in Cystic Fibrosis
... model systems of differential gene and protein expression in CF versus non-CF controls. Taken together, proteomic studies suggest alterations in pathways that are similar to those observed in gene-array ...
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canales de cloro como blancos de drogas
... in cystic fibrosis (CF) and activators of ∆F508-CFTR, the most common cF-causing ...| CF transmembrane regulator (CFTR) normally functions as a cyclic AMP-activated chloride channel at ...
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El nivel de ingresos bajos es un factor de riesgo importante en pacientes con fibrosis qustica del noreste de Mxico
... of Cystic Fibrosis (AMFQ, http:// ...1,200 CF cases in 25 years; this means that about 15% of them are diagnosed, six thousand of Mexican CF children do not have access to specialized treat- ...
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Vol. 89, Núm. 5 (2018)
... Introduction: Cystic fibrosis (CF) is an inherited, progressive, multisystem ...National CF Pro- gram of the Metropolitan Region, ...National CF Program; Tanner sexual maturity stage I, ...
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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. 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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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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Diferencias en la respuesta fisiológica durante la prueba de marcha 6 minutos y el test Glittre-ADL en pacientes con fibrosis quística: Estudio piloto
... deterioration of lung function and peripheral muscle dysfunction. In order to know this physical condition and to define the prognosis of the disease, a functional assessment should simulates activities of daily living. ...
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JOINT VENTURE PHILANTHROPY pdf
... Until now, the reimbursement on the investment of these foundations has been minimal. The Cystic Fibrosis Foundation has broken all previous paradigms. The increase in capital of these foundations can help ...
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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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Fibrosis quística, triple terapia pdf
... en el gen que codifica la síntesis de la proteína de membrana designada con el acrónimo CFTR (Cystic Fibrosis Trans-membrane Conductance Regulator). Estos estudios señalan que pronto será posible ofrecer ...
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