Volume 61 Issue 4 (2019)

Published: August 28, 2019

Review Article

Optic neuropathies in childhood: a review of etiology and treatment
Ceren Günbey, Bahadır Konuşkan
DOI: 10.24953/turkjped.2019.04.001
Pages: 471-476
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Original Articles

Fanconi anemia: a single center experience of a large cohort
Selman Kesici, Şule Ünal, Barış Kuşkonmaz, Selin Aytaç, Mualla Çetin, Fatma Gümrük
DOI: 10.24953/turkjped.2019.04.002
Pages: 477-484
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Factors affecting mortality in children with dilated cardiomyopathy
Muhammed Nurullah Sabaz, Alper Akın, Meki Bilici, Fikri Demir, Mehmet Türe, Hasan Balık
DOI: 10.24953/turkjped.2019.04.003
Pages: 485-492
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The potential utility of real-time PCR of the 16S-rRNA gene in the diagnosis of neonatal sepsis
Kenan İstanbullu, Nilgün Köksal, Merih Çetinkaya, Hilal Özkan, Tahsin Yakut, Mutlu Karkucak, Haldun Doğan
DOI: 10.24953/turkjped.2019.04.004
Pages: 493-499
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Expression of the Toll-like receptors 2 gene as a genetic determinant of the formation of newborns multiple organ failure syndrome
Dmytro A Shkurupii
DOI: 10.24953/turkjped.2019.04.005
Pages: 500-504
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Two years of newborn screening for cystic fibrosis in Turkey: Çukurova experience
Ayşe Şenay Şaşihüseyinoğlu, Derya Ufuk Altıntaş, Atıl Bişgin, Dilek Doğruel, Mustafa Yılmaz, Mahir Serbes
DOI: 10.24953/turkjped.2019.04.006
Pages: 505-512
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The contribution of morphine sulfate to the development of necrotizing enterocolitis in preterm infants: a matched casecontrol study
Zlatan Zvizdic, Emir Milisic, Asmir Jonuzi, Sabina Terzic, Denisa Zvizdic
DOI: 10.24953/turkjped.2019.04.007
Pages: 513-519
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Telomere length comparison between oral cells and blood cells among neonates
Mandar Bhattacharya, Pranami Bhaumik, Subrata Kumar-Dey
DOI: 10.24953/turkjped.2019.04.008
Pages: 520-524
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Cranial MR characteristics of Cerebral Palsy cases and correlation of findings with clinical results
Asuman Ali, Ramazan Yalçın, Ayşem Ünlüer-Gümüştaş
DOI: 10.24953/turkjped.2019.04.009
Pages: 525-537
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Stevens-Johnson syndrome and toxic epidermal necrolysis: a report of six cases
Ahu Kara, İlker Devrim, İlknur Çağlar, Nuri Bayram, Selcen Kundak, Hurşit Apa, Emir Volkan Altan
DOI: 10.24953/turkjped.2019.04.010
Pages: 538-543
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Eleven-year surveillance of acute flaccid paralysis in southwestern Iran
Ali Akbar Momen, Abdolhussein Shakurnia, Mehdi Momen
DOI: 10.24953/turkjped.2019.04.011
Pages: 544-551
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Reversible cardiomyopathy-tachycardiomyopathy in children
Alev Arslan, İlkay Erdoğan, Birgül Varan, Mustafa Yılmaz, Mehmet Bülent Özin, Niyazi Kürşad Tokel
DOI: 10.24953/turkjped.2019.04.012
Pages: 552-559
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Impulse oscillometry reference values and correlation with predictors in Turkish preschool children
İlkay Er, Ayla Günlemez, Canan Baydemir, Fatih Kılıçbay, Refika Ersu, Zeynep Seda Uyan
DOI: 10.24953/turkjped.2019.04.013
Pages: 560-567
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Relationships between screen time, internet addiction and other lifestyle behaviors with obesity among secondary school students in the Turkish Republic of Northern Cyprus
Özen Aşut, Gulifeiya Abuduxike, Songül Acar-Vaizoğlu, Sanda Cali
DOI: 10.24953/turkjped.2019.04.014
Pages: 568-579
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Case Reports

Unusual and early onset IPEX syndrome: a case report
Dilek Doğruel, Fatih Gürbüz, İhsan Turan, Derya Ufuk Altıntaş, Mustafa Yılmaz, Bilgin Yüksel
DOI: 10.24953/turkjped.2019.04.015
Pages: 580-584
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An adolescent case of extensive Behçet`s disease successfully treated with Infliximab
Emel Isıyel, Enver Hasanoğlu, Tuğba Şişmanlar, Ayşe Tana Aslan, Meltem Akçaboy, Yaşar Kandur, Çağrı Damar, Yeşim Özdemir, Öznur Boyunağa, İdil Yenicesu, Deniz Oğuz, Sevcan Bakkaloğlu, Necla Buyan
DOI: 10.24953/turkjped.2019.04.016
Pages: 585-588
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The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome
Semra Gürsoy, Yaşar Bekir Kutbay, Taha Reşid Özdemir, Filiz Hazan
DOI: 10.24953/turkjped.2019.04.017
Pages: 589-593
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A novel LEMD3 pathogenic variant in a son and mother with osteopoikilosis
Selin Elmaoğulları, Adelet Elçin Yıldız, Selma Demir, Hakan Gürkan, Seyit Ahmet Uçaktürk
DOI: 10.24953/turkjped.2019.04.018
Pages: 594-598
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The case of pyridoxine dependent epilepsy misdiagnosed as non-ketotic hyperglycinemia
Hande Gazeteci-Tekin, Melis Demir, Gül Aktan, Hasan Tekgül, Sarenur Gökben
DOI: 10.24953/turkjped.2019.04.019
Pages: 599-603
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Netherton syndrome previously misdiagnosed as hyper IgE syndrome caused by a probable mutation in SPINK5 C
Kemal Özyurt, Mustafa Atasoy, Ragıp Ertaş, Yılmaz Ulaş, Muhammed Reşat Akkuş, Aslıhan Kiraz, Hans Christian Hennies
DOI: 10.24953/turkjped.2019.04.020
Pages: 604-607
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Could you say that was an atrial flutter or not?
Serkan Özsoylu, Başak Nur Akyıldız, Adem Dursun, Özge Pamukçu
DOI: 10.24953/turkjped.2019.04.021
Pages: 608-610
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What triggered massive hemoptysis in Goodpasture syndrome with isolated pulmonary involvement in a 14-year-old boy?
Tuğba Şişmanlar-Eyüboğlu, Ayşe Tana Aslan, Deniz Gezgin-Yıldırım, Necla Buyan, Serhat Emeksiz, Gökhan Kalkan
DOI: 10.24953/turkjped.2019.04.022
Pages: 611-614
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Alpha gal specific IgE positivity due to tick bites and red meat allergy: the first case report in Turkey
Şennur Keleş, Mehmet Gündüz
DOI: 10.24953/turkjped.2019.04.023
Pages: 615-617
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Complete atrioventricular block associated with clozapine intoxication: case report
Mehmet Türe, Meki Bilici, Alper Akın, Fikri Demir, Hasan Balık, Savaş Mert Darakçı
DOI: 10.24953/turkjped.2019.04.024
Pages: 618-621
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Medicolegal evaluation of a maternal filicide attempt: a case report
Dilşad Foto-Özdemir, Aysun Balseven-Odabaşı, Aysun Balseven-Odabaşı, Ferda Karadağ, Ramazan Akçan, Eda Yılmaz
DOI: 10.24953/turkjped.2019.04.025
Pages: 622-628
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Systemic hypertension followed by insidious stroke in a 12-year-old boy with childhood neurofibromatosis type 1 presenting with renal and cerebral artery vasculopathy
Meng-Luen Lee, Tung-Ming Chang, Rei-Cheng Yang, Albert D Yang, Ming Chen
DOI: 10.24953/turkjped.2019.04.026
Pages: 629-634
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Benign migratory glossitis
Satvinder Singh Bakshi
DOI: 10.24953/turkjped.2019.04.027
Pages: 635
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