Yazar "Kalayci, Ayhan G." için listeleme
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Assessment of Endothelial Dysfunction With Adhesion Molecules in Patients With Celiac Disease
Comba, Atakan; Caltepe, Gonul; Yanik, Keramettin; Gor, Ufuk; Yuce, Ozlem; Kalayci, Ayhan G. (Lippincott Williams & Wilkins, 2016)Objectives: Celiac disease (CD) is a systemic immune disorder. We assessed serum levels of adhesion molecules as a marker of endothelial dysfunction in patients with CD at first diagnosis and in those on a gluten free diet. ... -
Effects of age of diagnosis and dietary compliance on growth parameters of patients with celiac disease
Comba, Atakan; Caltepe, Gonul; Yuce, Ozlem; Eren, Esra; Kalayci, Ayhan G. (Soc Argentina Pediatria, 2018)Introduction. The objective of this study was to evaluate the relation between age at diagnosis and compliance to gluten free diet (GFD) on growth in children with celiac disease and the factors that influenced compliance ... -
The Frequency of Lysosomal Acid Lipase Deficiency in Children With Unexplained Liver Disease
Kuloglu, Zarife; Kansu, Aydan; Selbuz, Suna; Kalayci, Ayhan G.; Sahin, Gulseren; Kirsaclioglu, Ceyda Tuna; Isik, Ishak Abdurrahman (Lippincott Williams & Wilkins, 2019)Objectives: Evidence suggests that lysosomal acid lipase deficiency (LAL-D) is often underdiagnosed because symptoms may be nonspecific. We aimed to investigate the prevalence of LAL-D in children with unexplained liver ... -
Gallbladder Polyps: Rare Lesions in Childhood
Demirbas, Fatma; Caltepe, Gonul; Comba, Atakan; Bilgin, Meltem C.; Eren, Esra; Abbasguliyev, Hasan; Kalayci, Ayhan G. (Lippincott Williams & Wilkins, 2019)Objective: Unlike adults, gallbladder polyps (GPs) are rare in childhood. The aim of this study was to evaluate patients with a GP diagnosis. Methods: Patients who were diagnosed with GP via ultrasonography from October ... -
Retrospective analysis of children with-1 antitrypsin deficiency
Comba, Atakan; Demirbas, Fatma; Caltepe, Gonul; Eren, Esra; Kalayci, Ayhan G. (Lippincott Williams & Wilkins, 2018)Background-1 Antitrypsin (AAT) deficiency is the most frequently occurring genetic liver disorder. The association among classical -1 antitrypsin deficiency (AATD), chronic liver disease, and cirrhosis is common in adult ...
