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251.253  Articles
1 of 25.126 pages  |  10  records  |  more records»
The article is devoted to problems of diagnosis of cystic disease of breast at different ages including children and teens. Analyzed various options for classification of cystic changes.The main method of detecting liquid formation is breast ultrasound, t... see more

The operative treatment results of 26 patients with pseudocysts of pancreas were analyzed in the article. 2 groups of patients were singled out according to the analyses aim. Basic group - the patients, who were cured with help of transcutaneous technolog... see more

Background: Human hydatid disease imposes significant impacts on public health by producing substantial morbidity and mortality in involved communities. This study aimed to evaluate the epidemiology and clinical features of hydatid cyst in northern Iran a... see more

ABSTRAKSekitar 80-90% pasien cystic fibrosis akan mengalami pancreatic insuffiency. Keadaan ini akan menyebabkan terjadinya malabsorpsi lemak dan protein dan akan berpengaruh pada status nutrisi dari pasien. Terapi dari terjadinya pancreatic insufficiency... see more

Shydlovscky A. V. Treatment of cystic thyroid nodes through a combination of sclerotherapy and laser interstitial thermotherapy. Journal of Education, Health and Sport. 2015;5(4):41-51. ISSN 2391-8306. DOI: 10.5281/zenodo.16592http://ojs.ukw.edu.pl/index.... see more

Objectives: The surgical treatment of hydatid cyst varies fromsimple puncture and aspiration to radical resections and totalcystectomy. The aim of this study was to evaluate and compareoutcome of different surgical treatments of liver hydatid cystsin our ... see more

Background: Cystic Fibrosis (CF) is an autosomal recessive disorder of exocrine glands characterized by abnormal production of thick mucus, primar-ily in bronchi of the lungs. Individuals experience recurrent respiratory infections, increased work of brea... see more

Cystic fibrosis is one of the most prevalent inherited diseases. This disease is caused by a mutation in a membrane protein, the cystic fibrosis transmembrane conductance regulator (CFTR). CFTR is known to function as a chloride channel that regulates the... see more

Introduction: Inhalation therapy is a crucial part of the cystic fibrosis (CF) treatment regimen. Drugs that assist in mucociliary clearance and inhaled antibiotics are used by most patients. Methods: This is a cross-sectional study where patients with CF... see more

1 of 25.126 pages  |  10  records  |  more records»