Volume 47 Issue 3 (2005)

Published: September 28, 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
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 Balci, Filiz Ozbaş Gerçeker, Songül Aksoy, Gonca Sennaroğlu, Ersan Kalay, Levent Sennaroğlu, Pervin Dinçer
Pages: 213-221
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The first camps in Turkey for asthmatic children: six years' experience
Ulker Oneş, Nihat Sapan, Mehtap Yazicioğlu, Nermin Güler, Zeynep Tamay, Ayper Somer, Yakup Canitez
Pages: 222-226
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Use of polymerase chain reaction for detection of adenovirus in children with or without wheezing
Cansin Saçkesen, Ahmet Pinar, Bülent E Sekerel, Yakut Akyön, Yildiz Saraçlar
Pages: 227-231
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Prenatal echocardiographic diagnosis of congenital heart disease: comparison of past and current results
Süheyla Ozkutlu, Canan Ayabakan, Tevfik Karagöz, Lütfü Onderoğlu, Ozgür Deren, Melda Cağlar, Safak Güçer
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 Bayrakci, Fügen Ersoy, Ozden Sanal, Sebnem Kiliç, Ayşe Metin, Ilhan Tezcan
Pages: 239-246
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Spontaneous closure of small apical muscular ventricular septal defects
Semra Atalay, Ercan Tutar, Filiz Ekici, Nazire Naçar
Pages: 247-250
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Neutrophil hypersegmentation and thrombocytosis in children with iron deficiency anemia
Serpil Düzgün, Yildiz Yildirmak, Feyzullah Cetinkaya
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 Tanrikulu, Behçet Erol, Belgin Görgün, Murat Söker
Pages: 261-265
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Case Reports

A very rare cause of recurrent apnea: congenital nasopharyngeal teratoma
Zülal Ulger, Ayten Egemen, Bülent Karapinar, Ali Veral, Fazil Apaydin
Pages: 266-269
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Autoimmune thrombocytopenic purpura after mumps infection
Sule Unal, Sevgi Yetgin, Ateş Kara, Güler Kanra
Pages: 270-271
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Brucella melitensis in blood cultures of two newborns due to exchange transfusion
Mustafa Akçakuş, Duygu Esel, Neşide Cetin, Ayşenur Paç Kisaarslan, Selim Kurtoğlu
Pages: 272-274
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Startle disease-two sibling cases
Mürüvet Elkay, Faruk Incecik, M Ozlem Hergüner, Göksel Leblebisatan, Sakir Altunbaşak
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 Corapçioğlu, Kamer Mutafoğlu Uysal, Erdem Silistreli, Nurettin Unal, Hale Oren, Unal Açikel
Pages: 279-282
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Spontaneous rupture of choledochal cyst presenting in childhood
Demet Aydoğdu Kiresi, Aydin Karabacakoğlu, Alaaddin Dilsiz, Serdar Karaköse
Pages: 283-286
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Brain calcification due to secondary hyperparathyroidism in a child with chronic renal failure
Ilmay Bilge, Banu Sadikoğlu, Sevinç Emre, Aydan Sirin, Burak Tatli
Pages: 287-290
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A case of double-outlet left ventricle with atrioventricular discordance
Canan Ayabakan, Figen Akalin
Pages: 291-294
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Unilateral pulmonary agenesis associated with colloidal goiter in a newborn: a case report
Güzide Ayşe Gökhan, Gülay Ozbilim, Sevgi Bozova, Aşkin Güra, Hakan Ongun, Ercan Mihci, Gökhan Arslan
Pages: 295-297
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The triad of nesidioblastosis, congenital neuroblastoma and glomerulocystic disease of the newborn: a case report
Almila Bulun, S Umit Sarici, Ozge Uysal Soyer, Ozlem Tekşam, Murat Yurdakök, Melda Cağlar
Pages: 298-302
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