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Recurrent Salmonella Bacteremia in Interleukin-12 Receptor Beta 1 Deficiency
(Oxford Univ Press, 2006)
Interleukin-12 receptor beta 1 (IL12RB1) deficiency causes vulnerability to poorly virulent mycobacteria and nontyphoid Salmonella species. We describe a 2.5 year-old girl with IL12RB1 deficiency, caused by a homozygous; ...
Speech Delay In Toddlers: Are They Only "Late Talkers"?
(Turkish J Pediatrics, 2018)
Speech delay is prevalent in toddlers. Although some children with speech delay are able to catch up with their peers with time, the delay might be part of a broader condition such as global developmental delay, which ...
Seizures in a Pediatric Intensive Care Unit: A Prospective Study
(Oxford Univ Press, 2016)
Background: The aim of the research is to determine the etiology and clinical features of seizures in critically ill children admitted to a pediatric intensive care unit (PICU). Methods: A total of 203 children were admitted ...
Outcome Of Out-Of-Hospital Cardiopulmonary Arrest In Children: A Multicenter Cohort Study
(Turkish J Pediatrics, 2018)
The aim of this study was to evaluate the demographic characteristics of children who experienced out-of-hospital cardiopulmonary arrest (CPA), and to assess the impact of the bystander cardiopulmonary resuscitation (CPR) ...
Plasma Phthalate Levels in Pubertal Gynecomastia
(Amer Acad Pediatrics, 2010)
OBJECTIVE: Several untoward health effects of phthalates, which are a group of industrial chemicals with many commercial uses including personal-care products and plastic materials, have been defined. The most commonly ...
Predictors of Methotrexate Response in Turkish Children with Oligoarticular and Polyarticular Juvenile Idiopathic Arthritis
(Turkish J Pediatrics, 2017)
Methotrexate (MTX) is the most commonly used disease modifying antirheumatic drug in juvenile idiopathic arthritis (JIA). We aimed to define predictor factors for response to MTX in Turkish children with oligo- and ...
Management Strategies for Cln2 Disease
(Elsevier Science Inc, 2017)
CLN2 disease (neuronal ceroid lipofuscinosis type 2) is a rare, autosomal recessive, pediatric-onset, rapidly progressive neurodegenerative lysosomal storage disorder caused by tripeptidyl peptidase 1 (TPP1) enzyme deficiency, ...
Accidental Oral Administration of Povidone Iodine in A Newborn: Case Report
(Soc Argentina Pediatria, 2016)
Iodine solutions are widely used as antiseptic for treating and preventing wound infections. Povidone iodine, one of the most common topical iodine solutions in emergency kits, can lead to several abnormalities as thyroid ...
Prenatal-Onset Niemann-Pick Type C Disease with Nonimmune Hydrops Fetails
(Elsevier Taiwan, 2013)
Niemann-Pick type C (NPC; OMIM 257219) disease is a neurodegenerative lysosomal storage disorder characterized by accumulation of unesterified cholesterol in the lysosomal/late endosomal system. This autosomal recessive ...
Predictors of Self-Esteem in Adolescents with A Psychiatric Referral
(Turkish J Pediatrics, 2016)
In the literature self-esteem is found to be lower in clinically referred adolescents compared to adolescents without any psychiatric disorder. The aim of this study is to examine self-esteem and associated socio-demographical ...