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Mefv Mutations In Systemic Jia
(BioMed Central, 2008)
Background: Systemic form of juvenile idiopathic arthritis (JIA) is regarded as an autoinflammatory disease. Certain genetic polymorphisms in genes coding inflammatory proteins have been associated with the disease. On the ...
Parental Perception and Child's Nutritional Status
(Turkish J Pediatrics, 2016)
Childhood obesity is a health hazard increasing worldwide. Preschool period which is under supervision of parents is a critical period to detect overweight and take precautions. We studied the factors affecting parental ...
Delayed Neurologic Sequelae Of Carbon Monoxide Intoxication
(Elsevier, 2018)
Altered consciousness and accompanying neurological symptoms are both complex and challenging cases for emergency physicians. These are not specific and may be a sign of a variety of medical conditions including stroke and ...
Overweight/Obesity and Respiratory and Allergic Disease in Children: International Study of Asthma And Allergies In Childhood (Isaac) Phase Two
(PLOS, 2014)
BACKGROUND:
Childhood obesity and asthma are increasing worldwide. A possible link between the two conditions has been postulated.
METHODS:
Cross-sectional studies of stratified random samples of 8-12-year-old children ...
Determinants of Pre-Lacteal Feeding Practices in Urban And Rural Nigeria; A Population-Based Cross-Sectional Study Using The 2013 Nigeria Demographic And Health Survey Data
(Faculty of Medicine, Makerere University, 2017)
Background Prelacteal feeding (PLF) is a barrier to exclusive breast feeding. Objective To determine factors associated with PLF in rural and urban Nigeria. Methods We utilized data from the 2013 Nigerian Demographic and ...
Management of Hair Loss Associated with Endocrine Therapy in Patients with Breast Cancer: An Overview
(Springer, 2016)
Endocrine therapy-induced hair loss (ETIHL) associated with aromatase inhibitors and tamoxifen treatment is currently mostly reported but remained an unresolved therapeutic issue in patients with breast cancer (BC) since ...
Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause Of Neonatal Death, Explained By Tpit Gene Mutations
(Endocrine Soc, 2005)
Tpit is a T box transcription factor important for terminal differentiation of pituitary proopiomelanocortin-expressing cells. We demonstrated that human and mouse mutations of the TPIT gene cause a neonatal-onset form of ...
Pseudocoarctation of the Aorta
(J-Stage, 1990)
In this report 5 patients between the ages of 5-14 years admitted to the Department of Pediatric Cardiology, Hacettepe University, and diagnosed as having pseudocoarctation of the aorta arc presented. The clinical and ...
Uzamış Öksürüğü Olan Erişkinlerde Bordetella pertussis Enfeksiyonunun Serolojik Olarak Değerlendirilmesi
(Ankara Microbiology Soc, 2016)
Aşı ile önlenebilen bir hastalık olan boğmaca, enfekte bireylerden duyarlı kişilere solunum yolu ile bulaşmaktadır. Bordetella pertussis enfeksiyonuna karşı, aşı veya doğal enfeksiyon sonucu gelişen immün yanıt ömür boyu ...