Search Results - "Karabel, M"
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Surgical outcome of bronchiectasis in children: long term results of 60 cases
Published in Klinische Padiatrie (01-07-2014)“…Bronchiectasis is described as destruction and the irreversible dilatation of bronchial structure. We wanted to demonstrate our surgical practice and outcome…”
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The role of serum N-terminal pro-brain natriuretic peptide in transient tachypnea of the newborn
Published in European review for medical and pharmacological sciences (01-07-2013)“…Transient tachypnea of the newborn (TTN), also known as wet lung disease, is a common cause of respiratory distress in the newborn. It has been demonstrated…”
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Platelet parameters in children with upper urinary tract infection: is there a specific response?
Published in Renal failure (01-01-2008)“…Although complete blood count is routinely ordered in most upper urinary tract infections (UTI), and information regarding the patient's platelet indices is…”
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A newborn with trisomy 13 who had tetralogy of Fallot and metopic synostosis: Case report
Published in Hippokratia (01-01-2013)“…Trisomy 13 (Patau syndrome) was first described by Patau et al in 1960. It is characterized by serious head, facial, and extremity anomalies, congenital heart…”
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A perspective from the practice of swaddling by Turkish mothers
Published in Hippokratia (01-01-2012)“…The purpose of this study was to investigate the practice of swaddling by Turkish mothers residing in different areas of the country (rural or urban), and…”
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Analysis of mortality risk factors for newborns with Bochdalek diaphragmatic hernia a 10-year single-centre experience
Published in South African journal of surgery (01-09-2022)“…Background and objectives: In this study, we aimed to investigate the risk factors for mortality in Bochdalek diaphragmatic hernia (BDH) patients. Methods:…”
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Puffy Feet in an 11-month-old Infant: A Quiz
Published in Acta dermato-venereologica (2009)Get full text
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A newborn with trisomy 13 who had tetralogy of Fallot and metopic synostosis: Case report
Published in Hippokratia (01-07-2013)“…BACKGROUND AND AIMTrisomy 13 (Patau syndrome) was first described by Patau et al in 1960. It is characterized by serious head, facial, and extremity anomalies,…”
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