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The Turkish Journal of Pediatrics
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Volume: 47 - Issue: 3
Original Articles
Case Report
Original Articles
Overcoming difficulties in implementing a universal newborn hearing screening program
Stavros Korres
1,3
, Dimitrios G. Balatsouras
2,3
, Stamatia Vlachou
3
Ioannis G. Kastanioudakis
4
, Nausica V. Ziavra
4
, Eleftherios Ferekidis
4
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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
1
, Filiz Özbaş Gerçeker
2
, Songül Aksoy
3
, Gonca Sennaroğlu
3
, Ersan Kalay
4
Levent Sennaroğlu
5
, Pervin Dinçer
1
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The first camps in Turkey for asthmatic children: six years’ experience
Ülker Öneş
1
, Nihat Sapan
2
, Mehtap Yazıcıoğlu
3
, Nermin Güler
1
, Zeynep Tamay
1
, Ayper Somer
1
, Yakup Canıtez
2
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Use of polymerase chain reaction for detection of adenovirus in children with or without wheezing
Cansın Saçkesen
1
, Ahmet Pınar
2
, Bülent E Şekerel
1
, Yakut Akyön
2
, Yıldız Saraçlar
1
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Prenatal echocardiographic diagnosis of congenital heart disease: comparison of past and current results
Süheyla Özkutlu
1
, Canan Ayabakan
1
, Tevfik Karagöz
1
, Lütfü Önderoğlu
2
, Özgür Deren
2
, Melda Çağlar
1
, Şafak Güçer
1
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The efficacy of immunoglobulin replacement therapy in the longterm follow-up of the B-cell deficiencies (XLA, HIM, CVID)
Benan Bayrakcı
1
, Fügen Ersoy
1
, Özden Sanal
1
, Şebnem Kılıç
2
, Ayşe Metin
3
, İlhan Tezcan
1
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Spontaneous closure of small apical muscular ventricular septal defects
Semra Atalay, Ercan Tutar, Filiz Ekici, Nazire Naçar
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Neutrophil hypersegmentation and thrombocytosis in children with iron deficiency anemia
Serpil Düzgün, Yıldız Yıldırmak, Feyzullah Çetinkaya
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Familial ureteroceles: an evidence for genetic background?
Selami Sözübir, David Ewalt, William Strand, Linda A. Baker
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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
1
, Behçet Erol
1
, Belgin Görgün
1
, Murat Söker
2
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A very rare cause of recurrent apnea: congenital nasopharyngeal teratoma
Zülal Ülger
¹
, Ayten Egemen
¹
, Bülent Karapınar
¹
, Ali Veral
²
, Fazıl Apaydın
³
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Autoimmune thrombocytopenic purpura after mumps infection
Şule Ünal, Sevgi Yetgin, Ateş Kara, Güler Kanra
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Brucella melitensis in blood cultures of two newborns due to exchange transfusion
Mustafa Akçakuş
1
, Duygu Esel
2
, Neşide Çetin
1
, Ayşenur Paç Kısaarslan
1
, Selim Kurtoğlu
1
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Startle disease – two sibling cases
Mürüvet Elkay
1
, Faruk İncecik
2
, M. Özlem Hergüner
1
, Göksel Leblebisatan
1
Şakir Altunbaşak
1
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Catheter-associated recurrent intracardiac thrombosis and factor V Leiden mutation in a child with non-Hodgkin’s lymphoma
Funda Çorapçıoğlu
1
, Kamer Mutafoğlu Uysal
2
, Erdem Silistreli
3
, Nurettin Ünal
2
Hale Ören
2
, Ünal Açıkel
3
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Spontaneous rupture of choledochal cyst presenting in childhood
Demet Aydoğdu Kiresi
1
, Aydın Karabacakoğlu
1
, Alaaddin Dilsiz
2
, Serdar Karaköse
1
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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
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A case of double-outlet left ventricle with atrioventricular discordance
Canan Ayabakan, Figen Akalın
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Unilateral pulmonary agenesis associated with colloidal goiter in a newborn: a case report
Güzide Ayşe Gökhan
¹
, Gülay Özbilim
¹
, Sevgi Bozova
¹
, Aşkın Güra
²
Hakan Ongun
²
, Ercan Mıhcı
²
, Gökhan Arslan
³
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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
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