Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Sanda Nousia-Arvanitakis"'
Publikováno v:
Pediatrics International. 56:89-94
Background Optimal nutritional status (NS) in cystic fibrosis (CF) is associated with better lung function and increased overall survival. This study estimated the prevalence of malnutrition and obesity among CF patients in a tertiary center. Methods
Autor:
Assimina Galli-Tsinopoulou, Alexandra Fleva, Ekaterini Pavlitou-Tsiontsi, Norma Vavatsi-Christaki, Paraskevi Panagopoulou, Sanda Nousia-Arvanitakis
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 47:356-362
Objectives: To measure adiponectin serum levels in Greek children and adolescents and correlate them with body fat and insulin resistance. Patients and Methods: Forty-six obese prepubertal children (19 M, 27 F) and 34 obese adolescents (17 M, 17 F) a
Publikováno v:
Acta Paediatrica. 96:1521-1525
Aim: To prove the hypothesis that exocrine pancreatic function determines resting energy expenditure (REE) in cystic fibrosis (CF). Method: Thirty-eight CF individuals, 9–34 (19.98 ± 1.0) years, were divided into three groups: Six pancreatic suffi
Autor:
Charilaos Stylianou, George Koliakos, Sanda Nousia-Arvanitakis, Maria Fotoulaki, Assimina Galli-Tsinopoulou
Publikováno v:
Journal of Cystic Fibrosis. 6:293-296
BackgroundGhrelin and leptin are hormones implicated in energy balance coordination and body weight regulation. There are conflicting data regarding the levels and role of leptin while ghrelin has not been studied in CF. The aim of this study was to
Publikováno v:
Acta Paediatrica. 90:515-519
Cystic-fibrosis-related diabetes mellitus is frequently underdiagnosed and associated with deterioration of overall clinical status. The purpose of this prospective study was to investigate the influence of insulin on nutrition, lung function and cli
Autor:
Assimina Galli-Tsinopoulou, Tatiana Moudiou, Sanda Nousia-Arvanitakis, Michael Karamouzis, Apostolos Mamopoulos
Publikováno v:
Fertility and Sterility. 85:1484-1487
Objective To assess hormonal status and morphology of ovaries in cystic fibrosis (CF) adolescents. Design Prospective study. Setting University teaching hospital. Patient(s) Female adolescents: 18 with CF and 18 normal. Intervention(s) Transabdominal
Autor:
Orit Shevah, Christos Bechlivanides, Sanda Nousia-Arvanitakis, Assimina Galli-Tsinopoulou, Ioannis Tsinopoulos, Zvi Laron
Publikováno v:
HORMONES. 2:120-124
Laron-type dwarfism is an autosomal recessive disorder caused by deletions or mutations of the growth hormone receptor gene. It is characterized by high circulating levels of growth hormone (GH) and low levels of insulin-like growth factor I (IGF-I).
Autor:
M. Xefteri, Nicolaos Stangos, Ioannis Tsinopoulos, Kyriaki Tentzidou, Sanda Nousia-Arvanitakis, Nicolaos Roubies, Assimina Galli-Tsinopoulou
Publikováno v:
Documenta Ophthalmologica. 101:211-221
Hypovitaminosis A is associated with exocrine pancreatic insufficiency in cystic fibrosis. Peripheral retinal dysfunction is an early finding of vitamin A deficiency. We evaluated serum retinol and zinc as well as visual adaptation in 41 patients wit
Autor:
Sanda Nousia-Arvanitakis
Publikováno v:
Journal of Clinical Gastroenterology. 29:138-142
Cystic fibrosis (CF) is inherited as an autosomal recessive trait due to a mutated gene carried on the long arm of chromosome 7. The protein coded by the CF gene (CFTR) is an apical chloride channel that regulates active chloride transport across epi
Autor:
Vlachonikolis J, Zaramboukas T, Kanakoudi-Tsakalides F, Maria Fotoulaki, Sanda Nousia-Arvanitakis, Augoustidou-Savvopoulou P
Publikováno v:
Digestive Diseases and Sciences. 44:2133-2138
The aim of this study was to investigate anti-gliadin (IgA-AGA and IgG-AGA), endomysial (IgA-EmA), and anti-reticulin (Ig-ARA) antibodies for monitoring celiac disease (CD) patients while on gluten-free and gluten-containing diets. Sera from 30 confi