Search Results - "Antônio F. Ribeiro"

The Use of Ultrasound as a Tool to Evaluate Pulmonary Disease in Cystic Fibrosis by Peixoto, Andressa O, Marson, Fernando Al, Dertkigil, Sérgio Sj, Dertkigil, Raquel P, Souza, Tiago H, Fraga, Andrea Ma, Ribeiro, Antônio F, Toro, Adyléia Adc, Ribeiro, José D

“…Lung ultrasound is an examination that allows the assessment of pulmonary involvement by analyzing artifacts. Our primary aim was to correlate our lung…”
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Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis by Sousa, Marisa, Servidoni, Maria F, Vinagre, Adriana M, Ramalho, Anabela S, Bonadia, Luciana C, Felício, Verónica, Ribeiro, Maria A, Uliyakina, Inna, Marson, Fernando A, Kmit, Arthur, Cardoso, Silvia R, Ribeiro, José D, Bertuzzo, Carmen S, Sousa, Lisete, Kunzelmann, Karl, Ribeiro, Antônio F, Amaral, Margarida D

“…Cystic Fibrosis (CF) is caused by ∼1,900 mutations in the CF transmembrane conductance regulator (CFTR) gene encoding for a cAMP-regulated chloride (Cl(-))…”
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Secretory IgA response against Pseudomonas aeruginosa in the upper airways and the link with chronic lung infection in cystic fibrosis by Mauch, Renan M., Rossi, Claudio L., Aiello, Talita B., Ribeiro, José D., Ribeiro, Antônio F., Høiby, Niels, Levy, Carlos E.

“…Abstract We assessed the diagnostic ability of an enzyme-linked immunosorbent assay test for measurement of specific secretory IgA (sIgA) in saliva to identify…”
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Prevalence and clinical outcomes of nontuberculous mycobacteria in a Brazilian cystic fibrosis reference center by Aiello, Talita B, Levy, Carlos E, Zaccariotto, Tânia R, Paschoal, Ilma A, Pereira, Mônica C, Nolasco da Silva, Marcos T, Ribeiro, José D, Ribeiro, Antônio F, Toro, Adyléia A D C, Mauch, Renan M

“…Abstract Nontuberculous mycobacteria (NTM) have been well established as an opportunistic pathogenic bacterial group for cystic fibrosis (CF) patients, with a…”
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Polymorphisms in ADRB2 gene can modulate the response to bronchodilators and the severity of cystic fibrosis by Marson, Fernando A L, Bertuzzo, Carmen S, Ribeiro, Antônio F, Ribeiro, José D

“…The most common cystic fibrosis (CF) manifestation is the progressive chronic obstructive pulmonary disease caused by deficiency, dysfunction, or absence of…”
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Lymphocyte responses to Mycobacterium tuberculosis and Mycobacterium bovis are similar between BCG-vaccinated patients with cystic fibrosis and healthy controls by Mauch, Renan M., Alves, Paulo César M., Levy, Carlos E., Ribeiro, José D., Ribeiro, Antônio F., Høiby, Niels, Nolasco da Silva, Marcos T.

“…•Lymphocyte proliferation against Mycobacterium tuberculosis and Mycobacterium bovis (BCG) has similar intensity between Brazilian CF patients and healthy…”
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Lung disease and vitamin D levels in cystic fibrosis infants and preschoolers by Oliveira, Marina S., Matsunaga, Natasha Y., Rodrigues, Marina L. E., Morcillo, André M., de Oliveira Ribeiro, Maria A. G., Ribeiro, Antônio F., C. P. Servidoni, Maria, Nogueira, Roberto José N., Pereira, Monica Corso, Ribeiro, José Dirceu, Toro, Adyléia Aparecida D. C.

“…Introduction Vitamin D acts on the immune system and lung response. Patients with cystic fibrosis (CF) may be deficient in this vitamin. The aims of the study…”
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The ACE gene D/I polymorphism as a modulator of severity of cystic fibrosis by Marson, Fernando A L, Bertuzzo, Carmen S, Hortencio, Taís D R, Ribeiro, José D, Bonadia, Luciana C, Ribeiro, Antônio F

“…Cystic Fibrosis (CF) is a monogenic disease with complex expression because of the action of genetic and environmental factors. We investigated whether the ACE…”
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Rectal forceps biopsy procedure in cystic fibrosis: technical aspects and patients perspective for clinical trials feasibility by Servidoni, Maria F, Sousa, Marisa, Vinagre, Adriana M, Cardoso, Silvia R, Ribeiro, Maria A, Meirelles, Luciana R, de Carvalho, Rita B, Kunzelmann, Karl, Ribeiro, Antônio F, Ribeiro, José D, Amaral, Margarida D

“…Measurements of CFTR function in rectal biopsies ex vivo have been used for diagnosis and prognosis of Cystic Fibrosis (CF) disease. Here, we aimed to evaluate…”
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Abernethy malformation: One of the etiologies of hepatopulmonary syndrome by Alvarez, Alfonso E., Ribeiro, Antônio F., Hessel, Gabriel, Baracat, Jamal, Ribeiro, José D.

“…Hepatopulmonary syndrome (HPS) is the clinical relationship between hepatic disease and the existence of pulmonary vascular dilatations, which can result in a…”
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Muscle satellite cells and impaired late stage regeneration in different murine models for muscular dystrophies by Ribeiro, Antonio F., Souza, Lucas S., Almeida, Camila F., Ishiba, Renata, Fernandes, Stephanie A., Guerrieri, Danielle A., Santos, André L. F., Onofre-Oliveira, Paula C. G., Vainzof, Mariz

“…Satellite cells (SCs) are the main muscle stem cells responsible for its regenerative capacity. In muscular dystrophies, however, a failure of the regenerative…”
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Cross-cultural adaptation and validation of the CFAbd-Score for gastrointestinal symptoms in patients with cystic fibrosis by Infantes, Flávia N.S., Lomazi, Elizete A., Zagoya, Carlos, Duckstein, Franziska, Magro, Daniela O., Pessotto, Fernando, Ribeiro, Antônio F., Ribeiro, José D., Mainz, Jochen G.

“…Translating and cross-culturally adapting the CFAbd-Score, Cystic Fibrosis (CF) Abdominal Score, to use in Brazilian spoken Portuguese. The CFAbd-Score is a…”
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CHARMIE: A Collaborative Healthcare and Home Service and Assistant Robot for Elderly Care by Ribeiro, Tiago, Gonçalves, Fernando, Garcia, Inês S., Lopes, Gil, Ribeiro, António F.

“…The global population is ageing at an unprecedented rate. With changes in life expectancy across the world, three major issues arise: an increasing proportion…”
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Cystic fibrosis at a Brazilian center of excellence: clinical and laboratory characteristics of 104 patients and their association with genotype and disease severity by Alvarez, Alfonso E, Ribeiro, Antonio F, Hessel, Gabriel, Bertuzzo, Carmen S, Ribeiro, José D

“…To identify the clinical, laboratory and radiographic characteristics of the cystic fibrosis patients under care at Universidade Estadual de Campinas (UNICAMP)…”
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Prevalence of constipation in cystic fibrosis patients: a systematic review of observational studies by Stefano, Marina A., Poderoso, Rosana E., Mainz, Jochen G., Ribeiro, Jose D., Ribeiro, Antonio F., Lomazi, Elizete Aparecida

“…To systematically revise the literature in search of data about the prevalence of constipation in patients with cystic fibrosis according to the publications…”
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Muscle Satellite Cells: Exploring the Basic Biology to Rule Them by Keith Okamoto, Oswaldo, Ribeiro Junior, Antonio F., Fernandes, Stephanie A., Almeida, Camila F., Vainzof, Mariz

“…Adult skeletal muscle is a postmitotic tissue with an enormous capacity to regenerate upon injury. This is accomplished by resident stem cells, named satellite…”
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VIVER COM FIBROSE CÍSTICA: A VISÃO PESSOAL DO ADOLESCENTE BRASILEIRO by Aguiar, Katia CA, Nucci, Nely AG, Marson, Fernando AL, Hortencio, Tais DR, Ribeiro, Antonio F, Ribeiro, Jose D

“…O presente estudo examinou os desafios psicológicos de adolescentes com fibrose cística (FC) no Brasil, por meio de uma entrevista semiestruturada com…”
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Distal intestinal obstruction syndrome: a diagnostic and therapeutic challenge in cystic fibrosis by Sandy, Natascha S., Massabki, Lilian H.P., Gonçalves, Aline C., Ribeiro, Antonio F., Ribeiro, Jose D., Servidoni, Maria de Fátima C.P., Lomazi, Elizete A.

“…To evaluate the demographics, genotype, and clinical presentation of pediatric patients presenting with distal intestinal obstruction syndrome (DIOS), and…”
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Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin-deficient mouse by Ishiba, Renata, Santos, André Luis F., Almeida, Camila F., Caires, Luiz Carlos, Ribeiro, Antonio F., Ayub-Guerrieri, Danielle, Fernandes, Stephanie A., Souza, Lucas S., Vainzof, Mariz

“…Dysferlin is a sarcolemmal muscle protein associated with the processes of membrane repair, trafficking, and fusion of intracellular vesicles and muscle…”
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The Impact of Cystic Fibrosis on the Immunologic Profile of Pediatric Patients by Bernardi, Daniela M., Ribeiro, Antonio F., Mazzola, Tais N., Vilela, Maria M.S., Sgarbieri, Valdemiro C.

“…To compare the immunologic state of 44 pediatric patients with cystic fibrosis (CF) with a control group consisting of 16 healthy individuals. CF patients aged…”
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