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Evolution and Prognostic Variables of Cystic Fibrosis in Children and Young Adults: A Narrative Review [PDF]
DiagnosticsIntroduction: Cystic fibrosis (CF) is a genetic condition affecting several organs and systems, including the pancreas, colon, respiratory system, and reproductive system.
Mădălina Andreea Donos +10 more
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Ileal Dieulafoy lesion arose 15 years after partial small bowel resection for meconium obstruction of the neonate: a case report [PDF]
BMC Pediatrics, 2021 Background Anastomotic or perianastomotic ulcers present with symptoms such as chronic anaemia and occult bleeding as long-term complications of bowel resection performed in infancy. Case presentation Herein, we describe a 15-year-old girl with a history
Maho Iwamoto +5 more
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Mucoviscidosis: fisiopatología, genética, aspectos clínicos y terapéuticos [PDF]
EMC Pediatria, 2020 Noël S, Sermet-Gaudelus I.
exaly +2 more sources
Innovative Therapies in Genetic Diseases: Cystic Fibrosis [PDF]
Romanian Journal of Pediatrics, 2021 Cystic fibrosis, also named mucoviscidosis, is the most frequent hereditary pulmonary disease and is produced by mutations in the CFTR gene, encoding an anionic channel for chloride and bicarbonate involved in the regulation of salt and bicarbonate ...
Elena-Silvia Shelby +7 more
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Both Ways at Once: Keeping Small Airways Clean. [PDF]
, 2017 The small airways of the lungs are under constant assault from the pathogens and debris in the air that they must conduct to alveoli. Although hygiene is of paramount importance for respiratory health, the underlying principles of airway clearance have ...
Quinton, Paul M
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Кубанский научный медицинский вестник, 2017 The comparative analysis of clinical and paraclinical features of mucoviscidosis flow in children of an early age in the Krasnodar region is presented in the article. The most frequent mutations found in mucoviscidosis’ patients are enumerated.
E. M. Shadrina +2 more
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Making It Last: Storage Time and Temperature Have Differential Impacts on Metabolite Profiles of Airway Samples from Cystic Fibrosis Patients. [PDF]
, 2017 Metabolites of human or microbial origin have the potential to be important biomarkers of the disease state in cystic fibrosis (CF). Clinical sample collection and storage conditions may impact metabolite abundances with clinical relevance.
John J. LiPuma +5 more
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Педиатрическая фармакология, 2012 This article is dedicated to a monogenic polysystemic disease — mucoviscidosis; its course severity and prognosis are to a large extend determined by the degree of lung affection, infection and chronic inflammatory process development in the airways. The
V. V. Chernikov, S. A. Krasovskiy
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Severe episodes of extra cellular dehydration : an atypical adult presentation of cystic fibrosis [PDF]
, 2008 Cystic fibrosis (CF) is usually diagnosed during childhood by respiratory or gastro-intestinal symptoms. Hyponatremic hypochloremic dehydration with metabolic alkalosis is a rare but typical presentation of CF in infants.
F. Illouz +5 more
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