The Turkish Journal of Pediatrics
2018 , Vol 60 , Num 3
GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria
Tülay Öncü-Öner, Aycan Ünalp, İlknur Porsuk-Doru, Sinem Ağılkaya, Handan Güleryüz, Aydan Saraç, Bekir Ergüner, Bayram Yüksel, Semra Hız-Kurul, Sultan Cingöz
DOI :
10.24953/turkjped.2018.03.001
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Efficacy of rufinamide in childhood refractory epilepsy
Edibe Pembegül Yıldız, Zeynep Hızlı, Gonca Bektaş, Melis Ulak-Özkan, Burak Tatlı, Nur Aydınlı, Mine Çalışkan, Meral Özmen
DOI :
10.24953/turkjped.2018.03.002
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Glycemic control and health behaviors in adolescents with type 1 diabetes
Aylin Yetim, Müjgan Alikaşifoğlu, Firdevs Baş, Kayı Eliaçık, Gülnaz Çığ, Ethem Erginöz, Oya Ercan, Rüveyde Bundak
DOI :
10.24953/turkjped.2018.03.003
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The influence of media on the sleep quality in adolescents
Duygu Akçay, Bülent Devrim Akçay
DOI :
10.24953/turkjped.2018.03.004
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Hereditary spherocytosis: Retrospective evaluation of 65 children
Ali Güngör, Neşe Yaralı, Ali Fettah, İkbal Ok-Bozkaya, Namık Özbek, Abdurrahman Kara
DOI :
: 10.24953/turkjped.2018.03.005
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Advantage of the subcutaneous immunoglobulin replacement therapy in primary immunodeficient patients with or without secondary protein loss
Pınar Gür-Çetinkaya, Deniz Nazire Çağdaş-Ayvaz, Ayça Burcu Öksüz, Ayşe Ertoy, Umut Hayran, Feride Özkan, Meliha Erol, İlhan Tezcan
DOI :
10.24953/turkjped.2018.03.006
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High alert medications administration errors in neonatal intensive care unit: A pediatric tertiary hospital experience
John Rene Labib, Meray Rene Labib Youssef, Shaimaa A.M. Abd El Fatah
DOI :
10.24953/turkjped.2018.03.007
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Gelsolin levels in patients with bronchiolitis
Feyza Hüsrevoğlu-Esen, Yasemin Altuner-Torun, Çiğdem Karakükçü, Seçil Köse, Ahmet Şehriyaroğlu, Dilek Kafadar, Aydın Esen, Mehmet Köse
DOI :
10.24953/turkjped.2018.03.008
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Attitudes of physicians concerning vaccines not included in the national immunization schedule
Tülin Çataklı, Aysu Duyan-Çamurdan, F. Nur Aksakal-Baran, Ahmet Enes Güven, Ufuk Beyazova
DOI :
10.24953/turkjped.2018.03.009
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Birth outcomes after inadvertent use of category X drugs contraindicated in pregnancy: Where is the real risk?
Zeynep Öztürk, Ercüment Ölmez, Tuğba Gürpınar, Kamil Vural
DOI :
10.24953/turkjped.2018.03.010
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Neonatal atrial flutter: Three cases and review of the literature
Seda Yılmaz-Semerci, Helen Bornaun, Dilek Kurnaz, Burcu Cebeci, Aslan Babayigit, Gökhan Büyükkale, Merih Çetinkaya
DOI :
10.24953/turkjped.2018.03.011
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A case of steroid-resistance Hashimoto's encephalopathy presenting with sensorimotor polyneuropathy
Serhat Emeksiz, Nurettin Onur Kutlu, Nuri Alaçakır, Hüseyin Çaksen
DOI :
10.24953/turkjped.2018.03.012
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A novel mutation of the MYH7 gene in a patient with hypertrophic cardiomyopathy
Nicholas Goel, Charles B. Huddleston, Andrew C. Fiore
DOI :
10.24953/turkjped.2018.03.013
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A case of atypically located leiomyoma mimicking axillary lymphadenomegaly
Mehmet Nuri Cevizci, Ali Fettah, Mehmet Eşref Kabalar
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10.24953/turkjped.2018.03.014
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A case of myeloid sarcoma presenting with an orbital mass, hearing loss, and multiple cranial neuropathies
Seon-hee Lim, Hye-na Nam, Kyung-in Lim, In-sang Jeon
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10.24953/turkjped.2018.03.015
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Polyarteritis nodosa in case of familial Mediterranean fever
İbrahim Gökçe, Ülger Altuntaş, Deniz Filinte, Harika Alpay
DOI :
10.24953/turkjped.2018.03.016
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An infant case of renovascular hypertension in moyamoya disease treated by angioplasty
Jianming Guo, Lianrui Guo, Gao Zeng, Zhu Tong, Xixiang Gao, Yongquan Gu
DOI :
10.24953/turkjped.2018.03.017
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Chelation therapy for secondary neonatal iron over load: Lessons learned from rhesus hemolytic disease
Fareed Khdair-Ahmad, Tariq Aladily, Olfat Khdair-Ahmad, Eman F. Badran
DOI :
10.24953/turkjped.2018.03.018
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Granulomatous amebic encephalitis caused by Acanthamoeba in an immuncompetent child
Murat Sütçü, Hacer Aktürk, Sezen Gülümser-Şişko, Manolya Acar, Oğuz Bülent Erol, Ayper Somer, Bilge Bilgiç, Nuran Salman
DOI :
10.24953/turkjped.2018.03.019
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Arthropathy-like findings and a carpal tunnel syndrome as the presenting features of Scheie syndrome: Three cases from the same family
Songül Gökay, Fatih Kardaş, Mustafa Kendirci, Betül Sözeri
DOI :
10.24953/turkjped.2018.03.020
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