Zobrazeno 1 - 10 of 36 pro vyhledávání: '"Stavros, Doudounakis"'
1
Adherence to Dietary Recommendations, Nutrient Intake Adequacy and Diet Quality among Pediatric Cystic Fibrosis Patients: Results from the GreeCF Study
Autor: Panagiota Devetzi, Stavros Doudounakis, Athanasios G. Kaditis, Maria G. Grammatikopoulou, Theodora Papamitsou, Dimitrios Poulimeneas, Tonia Vassilakou, Argyri Petrocheilou
Publikováno v: Nutrients
Volume 12
Issue 10
Nutrients, Vol 12, Iss 3126, p 3126 (2020)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nutrition is an important component of cystic fibrosis (CF) therapy, with a high-fat diet being the cornerstone of treatment. However, adherence to the dietary recommendations for CF appears suboptimal and burdensome for most children and adolescents
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::625492f7d7e8339d2e05c6cc96d934dc
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2
Comparison of International Growth Standards for Assessing Nutritional Status in Cystic Fibrosis: The GreeCF Study
Autor: Argyri Petrocheilou, Tonia Vassilakou, Athanasios G. Kaditis, Dimitrios Poulimeneas, Evgenia Troupi, Dimitrios Laggas, Stavros Doudounakis, Maria G. Grammatikopoulou
Publikováno v: Journal of pediatric gastroenterology and nutrition. 71(1)
Objective The aim of the study was to compare 3 international growth references and explore their differences in assessing growth in Greek school-aged patients with cystic fibrosis (CF). Methods Sample included 114 patients (50 boys, age 11.5 ± 3.9
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https://pubmed.ncbi.nlm.nih.gov/32102088
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3
Hyperthyrotropinemia in newly diagnosed cystic fibrosis patients with pancreatic insufficiency reversed by enzyme therapy
Autor: Christina Kanaka-Gantenbein, Theodore Karakonstantakis, Anni Katelaris, M. Noni, Aris Giannakopoulos, Stavros Doudounakis
Publikováno v: European Journal of Pediatrics. 177:775-779
Patients with cystic fibrosis (CF) commonly present with an elevated TSH concentration, suggesting subclinical hypothyroidism. Its relation to concomitant pancreatic insufficiency and its natural course upon initiation of enzyme replacement have not
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https://doi.org/10.1007/s00431-018-3120-3
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4
High attainment of optimal nutritional and growth status observed among Greek pediatric cystic fibrosis patients: results from the GreeCF study
Autor: Argiri Petrocheilou, Stavros Doudounakis, Maria G. Grammatikopoulou, Dimitrios Poulimeneas, Tonia Vassilakou, Ioanna Loukou, Dimitrios Laggas, Athanasios G. Kaditis
Publikováno v: Journal of Pediatric Endocrinology and Metabolism. 30
BACKGROUND Pediatric cystic fibrosis (CF) patients suffer high rates of undernutrition, subject to several parameters. We aimed to assess growth and nutritional status of Greek children and adolescents with CF. METHODS Eighty-four patients (35 boys)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69958171c44531b653efdd20cbf2a51e
https://doi.org/10.1515/jpem-2017-0013
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5
Comparison of two methods of measurement of maximal respiratory pressures in health and cystic fibrosis
Autor: Stavros Doudounakis, Gabriel Dimitriou, Theodore Dassios, A. Katelari
Publikováno v: Journal of Biomedical Science and Engineering. :43-48
Introduction: Respiratory muscle strength can be assessed by static mouth measurements of maximal inspiratory pressure (Pimax) and maximal expiratory pressure (Pemax). Impaired respiratory muscle strength is common in neuromuscular and obstructive pu
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https://doi.org/10.4236/jbise.2013.68a2006
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6
Study of Greek children and youths with cystic fibrosis identifies immunisation gaps and delays
Autor: Kalliopi Tanou, Maria Lekaditi, Maria Theodoridou, Helena C. Maltezou, Stavros Doudounakis, Panos Katerelos
Publikováno v: Acta paediatrica (Oslo, Norway : 1992). 106(2)
Aim Data about immunisation rates in cystic fibrosis (CF) patients are scarce. We estimated the rates and timeliness of immunisations in CF patients aged 0.55–22 years. Methods We studied 122 subjects at a hospital in Greece in 2014. A standard que
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73f58685e34b1f5bcc5b845ce9915766
https://pubmed.ncbi.nlm.nih.gov/27862309
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7
Respiratory muscle function in patients with cystic fibrosis
Autor: A. Katelari, Stavros Doudounakis, Stefanos Mantagos, Theodore Dassios, Gabriel Dimitriou
Publikováno v: Pediatric Pulmonology. 48:865-873
Respiratory muscle function in patients with cystic fibrosis (CF) can be assessed by measurement of maximal inspiratory pressure (Pimax ), maximal expiratory pressure (Pemax ), and pressure-time index of the respiratory muscles (PTImus ). We investig
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https://doi.org/10.1002/ppul.22709
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8
Voriconazole pharmacokinetics and photosensitivity in children with cystic fibrosis
Autor: Stavros Doudounakis, A. Katelari, Eleni Pappa, Sophia L. Markantonis
Publikováno v: Journal of Cystic Fibrosis. 11(3):246-252
BackgroundA high incidence of adverse skin reactions following long-term oral administration of voriconazole in children with cystic fibrosis and allergic bronchopulmonary aspergillosis (ABPA). The aim was to study the pharmacokinetics of voriconazol
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9
Hyperglycaemia and insulinopenia in a neonate with cystic fibrosis
Autor: Stavros Doudounakis, Dimitris Anagnostakis, Tania Siahanidou, Helen Mandyla
Publikováno v: Acta Paediatrica. 94:1837-1840
UNLABELLED Abnormal glucose tolerance is a frequent late complication of cystic fibrosis (CF), but the prevalence of CF-related diabetes mellitus (CFRD) in children less than 10 y old is less than 2%. The youngest child with CFRD reported to date was
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https://doi.org/10.1111/j.1651-2227.2005.tb01864.x
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10
The effect of vitamin K supplementation on biochemical markers of bone formation in children and adolescents with cystic fibrosis
Autor: Polyxeni Nicolaidou, Dimitrios Gourgiotis, Kostas N. Priftis, Anna Papadopoulou, Ioanna Loukou, Helen Georgouli, Ilias Stavrinadis, Yiannis G. Matsinos, Konstantinos Douros, Stavros Doudounakis
Publikováno v: European Journal of Pediatrics. 165:540-545
Impaired vitamin K status in cystic fibrosis (CF) has been considered as a newly emerged pathogenetic factor for reduced bone mineral density (BMD).Our aim was to evaluate the effectiveness of vitamin K supplementation in managing bone formation abno
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb9ecbc93d37d71656f392e53329867d
https://doi.org/10.1007/s00431-006-0132-1
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