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Toplam kayıt 6, listelenen: 1-6
A Rare COVID-19 Presentation; Relapse of Nephrotic Syndrome in a Pediatric Patient
(Erciyes University Faculty of Medicine, 2022)
Background: In early 2020, severe acute respiratory syndrome-corona virus 2 (SARS-CoV-2) pandemics caused previously unheard of health, social, and economic problems worldwide. The disease can affect different organs such ...
Evaluation of mediterranean diet adherence in children diagnosed with pancreatitis: A case-control study [Evaluación de la adhesión a la dieta mediterránea en niños diagnosticados de pancreatitis: Estudio de casos y controles]
(ARAN Ediciones S.A., 2021)
Background: the incidence of childhood acute pancreatitis has been increasing in the last two decades. The number of studies on the effects of diet on the pathogenesis of pancreatitis is very small. The aim of this study ...
Life quality and empathy in children with celiac disease
(Kare Publ, 2020)
OBJECTIVE: This study aims to investigate the associations between celiac disease (CD) and children's life quality and empathy level. METHODS: In this study, all participants aged 8-14 years completed the Turkish version ...
Comparison of screen time and digital gaming habits of Turkish children before and during the coronavirus disease 2019 pandemic
(Aves, 2021)
Objective: The aim of this study is to compare the screen time and digital gaming habits of Turkish children before and during the coronavirus disease 2019 (COVID-19) pandemic. Material and Methods: This cross-sectional ...
A rare complication of lightning strike: Pulmonary contusion
(Kare Yayıncılık, 2021)
Lightning strike is a devastating disaster, leading to various life-threating complications and even death. In lightning striking victims, high-voltage electric current can destroy many tissues and organs through various ...
Genotype to Phenotype: Identification of Mucopolysaccharidosis Type IIIB (Sanfilippo's B) Case Using Whole Exome Sequencing
(Georg Thieme Verlag Kg, 2021)
Mucopolysaccharidosis type IIIB (Sanfilippo's B; OMIM no.: 252920) is a lysosomal storage disorder caused by defective degradation of heparan sulfate. The enzyme that has decreased function in this disease is alpha-N ...