ISSN: 1306 - 0015 • E-ISSN: 1306 - 6278

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Turk Pediatri Ars : ()

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ORIGINAL ARTICE
1.Comparison of patients with familial mediterranean fever and juvenile ıdiopathic arthritis according to family origin
Kenan Barut, Gizem Pamuk, Amra Adrovic, Sezgin Şahin, Aslı Kaplan, Mürüvet Güler, Özgür Kasapçopur
doi: 10.5152/TurkPediatriArs.2017.5818  Page 

CASE REPORT
2.A Case of laryngeal atresia accompanied with persistent pharyngotracheal ductus
Levent Korkmaz, Işın Güneş, Hülya Halis, Ibrahim Ketenci, Osman Baştuğ, Mehmet Said Doğan, Mustafa Ali Akın
doi: 10.5152/TurkPediatriArs.2018.4619  Page 

3.A case of Type 1 Dent disease presenting with isolated persistant proteinuria
Tülin Güngör, Fehime Kara Eroğlu, Fatma Yazılıtaş, Gökçe Gür, Evrim Kargın Çakıcı, Michael Ludwig, Mehmet Bülbül
doi: 10.5152/TurkPediatriArs.2018.6540  Page 

4.A rare casue of brachial plexopathy: hereditary neuralgic amyotrophy
Hepsen Mine Serin, Sanem Yılmaz, Seda Kanmaz, Erdem Şimşek, Gül Serdaroğlu, Hasan Tekgül, Sarenur Gökben
doi: 10.5152/TurkPediatriArs.2018.5837  Page 

5.A rare structural myopathy: nemaline myopathy
Osman Yeşilbaş, Esra Şevketoğlu, Hasan Serdar Kıhtır, Melike Ersoy, Mey Talip Petmezci, Canan Hasbal Akkuş, Önder Şahin, Serdar Ceylaner
doi: 10.5152/TurkPediatriArs.2018.4402  Page 

6.A rare vascular lesion of newborn: cutis marmorata telangiectatica congenita
Ezgi Yangın Ergon, Kıymet Çelik, Rüya Çolak, Senem Alkan Özdemir, Özgür Olukman, Selcen Kundak, Şebnem Çalkavur
doi: 10.5152/TurkPediatriArs.2018.5557  Page 

7.An overlooked case of a treatable hyperinsulinemic hypoglycemia: congenital glycosylation defect type ıb
Pınar Haznedar, F Tuba Eminoğlu
doi: 10.5152/TurkPediatriArs.2018.18004  Page 

8.Chronic recurrent multifocal osteomyelitis: a Case report
Esma Altınel Açoğlu, Meltem Akçaboy, Yasemin Taşçı Yıldız, Nedim C M Gülaldı, Eyüp Sarı, Pelin Zorlu, Saliha Şenel
doi: 10.5152/TurkPediatriArs.2018.6590  Page 

9.Duane retraction syndrome in a patient with abnormal head position
Şule Gökçe, Zeynep Büşra Albayram, Gülizar Turan, Elif Demirkılınç Biler, Sema Aydoğdu
doi: 10.5152/TurkPediatriArs.2018.6116  Page 

10.Extreme delta brush activity; could it be a marker for early diagnosis and prognosis of anti- NMDA encephalitis?
Hande Gazeteci Tekin, Sarenur Gökben, Gül Serdaroğlu
doi: 10.5152/TurkPediatriArs.2018.4628  Page 

11.Giant aortic aneurysm due to fibulin- 4 deficiency: case series
Ayşe Sülü, Osman Başpınar, Derya Aydın Şahin
doi: 10.5152/TurkPediatriArs.2018.4658  Page 

12.Osteosarcoma of the rib: a case with rare presentation
Sema Büyükkapu Bay, Rejin Kebudi, Ayça Iribaş, Ömer Ömer Görgün, Fulya Ağaoğlu, Feryal Gün, Alaettin Çelik, Emin Darendeliler
doi: 10.5152/TurkPediatriArs.2017.4689  Page 

13.Pepper gas inhalation induced acute polyneuropathy mimicking Guillain-Barre syndrome
Sevgi Çıraklı, Mehmet Canpolat, Gül Demet Kaya Özçora, Selim Doğanay, Sefer Kumandaş
doi: 10.5152/TurkPediatriArs.2018.4375  Page 

14.SLC26A3 mutation in Turkish neonate and her sibling with congenital chloride diarrhea
Erkan Dogan, Eylem Sevinc, Mehmet Akif Göktaş, Sadrettin Ekmen, Nihal Yıldız, Mahmut Turgut
doi: 10.5152/TurkPediatriArs.2018.6929  Page 

15.Syncope due to complete atrioventricular block and treatment with a transient pacemaker in acute rheumatic fever: A case report
Mustafa Argun, Ali Baykan, Abdullah Özyurt, Özge Pamukçu, Kazım Üzüm, Nazmi Narin
doi: 10.5152/TurkPediatriArs.2018.4014  Page 

16.The clinical characteristics of fascioliasis in pediatric patients
Gülsüm Iclal Bayhan, Ayşegül Taylan Özkan, Yunus Emre Beyhan
doi: 10.5152/TurkPediatriArs.2018.6842  Page 

17.Unusual localisation and coincidence of primary hydatid cyst: a case report
Canan Kocaoğlu, Çelebi Kocaoğlu, Ayşe Yavuz, Aslan Akın
doi: 10.5152/TurkPediatriArs.2018.6200  Page 

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