Search Results - "Ucar, Sit"
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1
Evaluation of Etiology in Infants with Recurrent Pneumonia and Chronic Stridor
Published in Turkish Thoracic Journal/Türk Toraks Dergisi (01-07-2014)Get full text
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2
Hemophagocytosis: the cause of anemia and thrombocytopenia in congenital syphilis
Published in Pediatric hematology and oncology (01-01-2009)“…Congenital syphilis is a rare, serious disease that continues to be a major health-care problem. The infected neonate may be asymptomatic or multiple-organ…”
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3
Primary polydipsia case presenting with severe malnutrition
Published in Turk Pediatri Arsivi (01-09-2013)Get full text
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4
Pulmonary artery sling as a cause of recurrent wheezing in children
Published in Tüberküloz ve toraks (2010)“…Vascular rings are a group of aortic arch anomalies and usually presents with dispnea, stridor and feeding difficulties after birth. Pulmonary artery sling is…”
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5
HEMOPHAGOCYTOSIS: The Cause of Anemia and Thrombocytopenia in Congenital Syphilis
Published in Pediatric hematology and oncology (21-09-2009)“…Congenital syphilis is a rare, serious disease that continues to be a major health-care problem. The infected neonate may be asymptomatic or multiple-organ…”
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6
Jeune syndrome (asphyxiating thoracic dystrophy): a case report
Published in Tüberküloz ve toraks (2009)“…Jeune syndrome or asphyxiating thoracic dystrophy is a rare autosomal recessive skeletal dysplasia characterized by a small thorax, short-limbed dwarfism,…”
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7
Application of Flow Cytometry in the Early Diagnosis of Neonatal Sepsis
Published in Annals of clinical and laboratory science (01-03-2017)“…To raise awareness of the utility of flow cytometric detection of inflammatory markers in the early diagnosis of neonatal sepsis. In accordance with the…”
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8
Primary polydipsia case presenting with severe malnutrition/Agir beslenme bozuklugu ile basvuran birincil polidipsi olgusu
Published in Turk Pediatri Arsivi (01-09-2013)Get full text
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9
Hamartoma of the larynx: an unusual cause of stridor
Published in Balkan medical journal (01-12-2014)“…Hamartoma of the larynx is a very rare lesion, and the number of reported cases is limited. Signs and symptoms include stridor, changes in voice, eating and…”
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10
Thymic cyst causing acute respiratory failure and subtotal atelectasis in two-day-old baby: case report
Published in Türk göğüs kalp damar cerrahisi dergisi (15-04-2015)Get full text
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11
Niemann-Pick hastalığı tip A ve tip B: İki olgu sunumu
Published in Marmara Medical Journal (01-01-2014)Get full text
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12
Familyal Hemofagositik Lenfohistiositoz Tanılı İki Olgu
Published in The journal of pediatric research (05-06-2014)Get full text
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13
Jeune sendromu (asfiktik torasik displazi): Olgu sunumu
Published in Tüberküloz ve toraks (2009)“…Jeune sendromu veya asfiktik torasik distrofi, küçük göğüs kafesi, kısa ekstremiteli cücelik, hepatik ve renal anomaliler ile karakterize, otozomal resesif,…”
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14
Niemann-Pick hastalığı tip A ve tip B: İki olgu sunumu
Published in Marmara Medical Journal (01-01-2014)“…Niemann-Pick hastalığı, belirli dokularda, özellikle retiküloendotelyel hücrelerde, sfingolipidlerin biriktiği, konjenital lipidoz grubundan otozomal resesif…”
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15
Çocuklarda tekrarlayan hışıltının bir nedeni olarak pulmoner arter sling
Published in Tüberküloz ve toraks (2010)“…Vasküler ringler, bir grup aortik ark anomalisi olup genellikle doğumdan sonra solunum zorluğu, stridor ve beslenme güçlükleriyle ortaya çıkar. Pulmoner arter…”
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16
Ciddi bir yakınması olmaksızın başvuran üç aylık kız çocuğu
Published in Turk Pediatri Arsivi (2007)Get full text
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17
Maple Syrup Urine Disease Presenting with Bacterial Meningitis
Published in Türkiye çocuk hastalıkları dergisi (09-10-2015)Get full text
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18
A case of symptomatic aberrant right subclavian artery
Published in Erciyes tip dergisi (2008)“…Arkus aortayı oluşturan embriyonik yapıların involüsyonundaki anormallikler nedeni ile oluşan vasküler ringler, çocukluk çağında trakea ve özofagusu…”
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19
Progresif familyal intrahepatik kolestaz tip 3
Published in Türkiye Çocuk Hastalıkları Dergisi (2010)“…Progresif familyal intrahepatik kolestaz, biliyer siroz ve kolestaz ile karakterize bir grup hastalıktır. Süt ço- cuğu döneminde başlar ve yaşamın ilk on…”
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20
Üriner anomali ve işitme kaybının eşlik ettiği klippel-feil sendromu
Published in Yeni tıp dergisi (2008)“…Klippel-Feil sendromu, iki veya daha fazla servikal omurganın segmentasyon yetersizliği ile karakterize konjenital anomalidir. Bu sendrom, kısa boyun, düşük…”
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