The Turkish Journal of Pediatrics 2005 , Vol 47 , Num 3

Original Article (10)
Case Report (10)

Overcoming difficulties in implementing a universal newborn hearing screening program Stavros Korres,, Dimitrios G. Balatsouras,, Stamatia Vlachou Ioannis G. Kastanioudakis, Nausica V. Ziavra, Eleftherios Ferekidis Abstract Full Text:PDF Similar Articles Identification of an ancestral haplotype of the 35delG mutation in the GJB2 (connexin 26) gene responsible for autosomal recessive non-syndromic hearing loss in families from the Eastern Black Sea region in Turkey Burcu Balcı, Filiz Özbaş Gerçeker, Songül Aksoy, Gonca Sennaroğlu, Ersan Kalay Levent Sennaroğlu, Pervin Dinçer Abstract Full Text:PDF Similar Articles The first camps in Turkey for asthmatic children: six years’ experience Ülker Öneş, Nihat Sapan, Mehtap Yazıcıoğlu, Nermin Güler, Zeynep Tamay, Ayper Somer, Yakup Canıtez Abstract Full Text:PDF Similar Articles Use of polymerase chain reaction for detection of adenovirus in children with or without wheezing Cansın Saçkesen, Ahmet Pınar, Bülent E Şekerel, Yakut Akyön, Yıldız Saraçlar Abstract Full Text:PDF Similar Articles Prenatal echocardiographic diagnosis of congenital heart disease: comparison of past and current results Süheyla Özkutlu, Canan Ayabakan, Tevfik Karagöz, Lütfü Önderoğlu, Özgür Deren, Melda Çağlar, Şafak Güçer Abstract Full Text:PDF Similar Articles The efficacy of immunoglobulin replacement therapy in the longterm follow-up of the B-cell deficiencies (XLA, HIM, CVID) Benan Bayrakcı, Fügen Ersoy, Özden Sanal, Şebnem Kılıç, Ayşe Metin, İlhan Tezcan Abstract Full Text:PDF Similar Articles Spontaneous closure of small apical muscular ventricular septal defects Semra Atalay, Ercan Tutar, Filiz Ekici, Nazire Naçar Abstract Full Text:PDF Similar Articles Neutrophil hypersegmentation and thrombocytosis in children with iron deficiency anemia Serpil Düzgün, Yıldız Yıldırmak, Feyzullah Çetinkaya Abstract Full Text:PDF Similar Articles Familial ureteroceles: an evidence for genetic background? Selami Sözübir, David Ewalt, William Strand, Linda A. Baker Abstract Full Text:PDF Similar Articles The contribution to success of various methods of treatment of temporomandibular joint ankylosis (a statistical study containing 24 cases) Rezzan Tanrıkulu, Behçet Erol, Belgin Görgün, Murat Söker Abstract Full Text:PDF Similar Articles

A very rare cause of recurrent apnea: congenital nasopharyngeal teratoma Zülal Ülger¹, Ayten Egemen¹, Bülent Karapınar¹, Ali Veral², Fazıl Apaydın³ Abstract Full Text:PDF Similar Articles Autoimmune thrombocytopenic purpura after mumps infection Şule Ünal, Sevgi Yetgin, Ateş Kara, Güler Kanra Abstract Full Text:PDF Similar Articles Brucella melitensis in blood cultures of two newborns due to exchange transfusion Mustafa Akçakuş, Duygu Esel, Neşide Çetin, Ayşenur Paç Kısaarslan, Selim Kurtoğlu Abstract Full Text:PDF Similar Articles Startle disease – two sibling cases Mürüvet Elkay, Faruk İncecik, M. Özlem Hergüner, Göksel Leblebisatan Şakir Altunbaşak Abstract Full Text:PDF Similar Articles Catheter-associated recurrent intracardiac thrombosis and factor V Leiden mutation in a child with non-Hodgkin’s lymphoma Funda Çorapçıoğlu, Kamer Mutafoğlu Uysal, Erdem Silistreli, Nurettin Ünal Hale Ören, Ünal Açıkel Abstract Full Text:PDF Similar Articles Spontaneous rupture of choledochal cyst presenting in childhood Demet Aydoğdu Kiresi, Aydın Karabacakoğlu, Alaaddin Dilsiz, Serdar Karaköse Abstract Full Text:PDF Similar Articles Brain calcification due to secondary hyperparathyroidism in a child with chronic renal failure Ilmay Bilge, Banu Sadıkoğlu, Sevinç Emre, Aydan Şirin, Burak Tatlı Abstract Full Text:PDF Similar Articles A case of double-outlet left ventricle with atrioventricular discordance Canan Ayabakan, Figen Akalın Abstract Full Text:PDF Similar Articles Unilateral pulmonary agenesis associated with colloidal goiter in a newborn: a case report Güzide Ayşe Gökhan¹, Gülay Özbilim¹, Sevgi Bozova¹, Aşkın Güra² Hakan Ongun², Ercan Mıhcı², Gökhan Arslan³ Abstract Full Text:PDF Similar Articles The triad of nesidioblastosis, congenital neuroblastoma and glomerulocystic disease of the newborn: a case report Almıla Bulun, S. Ümit Sarıcı, Özge Uysal Soyer, Özlem Tekşam Murat Yurdakök, Melda Çağlar Abstract Full Text:PDF Similar Articles