Volume 47 Issue 3 (2005)

Published: July 25, 2005

Original Articles

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
DOI: 10.24953/turkjpediatr.2005.2716
Pages: 203-212
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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
DOI: 10.24953/turkjpediatr.2005.2717
Pages: 213-221
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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
DOI: 10.24953/turkjpediatr.2005.2718
Pages: 222-226
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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
DOI: 10.24953/turkjpediatr.2005.2719
Pages: 227-231
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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
DOI: 10.24953/turkjpediatr.2005.2720
Pages: 232-238
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The efficacy of immunoglobulin replacement therapy in the long-term follow-up of the B-cell deficiencies (XLA, HIM, CVID)
Benan Bayrakcı, Fügen Ersoy, Özden Sanal, Şebnem Kılıç, Ayşe Metin, İlhan Tezcan
DOI: 10.24953/turkjpediatr.2005.2721
Pages: 239-246
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Spontaneous closure of small apical muscular ventricular septal defects
Semra Atalay, Ercan Tutar, Filiz Ekici, Nazire Naçar
DOI: 10.24953/turkjpediatr.2005.2722
Pages: 247-250
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Neutrophil hypersegmentation and thrombocytosis in children with iron deficiency anemia
Serpil Düzgün, Yıldız Yıldırmak, Feyzullah Çetinkaya
DOI: 10.24953/turkjpediatr.2005.2723
Pages: 251-254
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Familial ureteroceles: an evidence for genetic background?
Selami Sözübir, David Ewalt, William Strand, Linda A. Baker
DOI: 10.24953/turkjped.2005.2724
Pages: 255-260
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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
DOI: 10.24953/turkjpediatr.2005.2725
Pages: 261-265
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Case Reports

A very rare cause of recurrent apnea: congenital nasopharyngeal teratoma
Zülal Ülger, Ayten Egemen, Bülent Karapınar, Ali Veral, Fazıl Apaydın
DOI: 10.24953/turkjpediatr.2005.2726
Pages: 266-269
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Autoimmune thrombocytopenic purpura after mumps infection
Şule Ünal, Sevgi Yetgin, Ateş Kara, Güler Kanra
DOI: 10.24953/turkjpediatr.2005.2727
Pages: 270-271
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Brucella melitensis in blood cultures of two newborns due to exchange transfusion
Mustafa Akçakuş, Duygu Esel, Neşide Çetin, Ayşenur Paç Kısaarslan, Selim Kurtoğlu
DOI: 10.24953/turkjpediatr.2005.2728
Pages: 272-274
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Startle disease-two sibling cases
Mürüvet Elkay, Faruk İncecik, M. Özlem Hergüner, Göksel Leblebisatan, Şakir Altunbaşak
DOI: 10.24953/turkjpediatr.2005.2729
Pages: 275-278
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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
DOI: 10.24953/turkjpediatr.2005.2730
Pages: 279-282
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Spontaneous rupture of choledochal cyst presenting in childhood
Demet Aydoğdu Kiresi, Aydın Karabacakoğlu, Alaaddin Dilsiz, Serdar Karaköse
DOI: 10.24953/turkjpediatr.2005.2731
Pages: 283-286
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Brain calcification due to secondary hyperparathyroidism in a child with chronic renal failure
Ilmay Bilge, Banu Sadıkoğlu, Sevinç Emre, Aydan Şirin, Burak Tatlı
DOI: 10.24953/turkjpediatr.2005.2732
Pages: 287-290
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A case of double-outlet left ventricle with atrioventricular discordance
Canan Ayabakan, Figen Akalın
DOI: 10.24953/turkjpediatr.2005.2733
Pages: 291-294
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Unilateral pulmonary agenesis associated with colloidal goiter in a newborn: a case report
Güzide Ayşe Gökhan, Gülay Özbilim, Sevgi Bozova, Aşkın Güra, Hakan Ongun, Ercan Mıhcı, Gökhan Arslan
DOI: 10.24953/turkjpediatr.2005.2734
Pages: 295-297
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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
DOI: 10.24953/turkjpediatr.2005.2735
Pages: 298-302
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