ISSN: 1306 - 0015 • E-ISSN: 1308 - 6278

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Turk Pediatri Ars : ()

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ORIGINAL ARTICE
1.Why the rate of perforated appendicitis is higher in girls unlike the literature in Eastern Turkey?
Veli Avcı, Kemal Ayengin
doi: 10.14744/TurkPediatriArs.2018.46548  Page 

2.Assessment of mothers’ measures against home accidents for 0–6-year-old children
Zehra Aslan Aydoğdu, Elif Ateş, Turan Set
doi: 10.14744/TurkPediatriArs.2019.64614  Page 

3.Behçet’s Disease in Childhood: Single Centre Experience
Murat Soner Çirkinoğlu, Selcan Demir, Yelda Bilginer, Seza Özen
doi: 10.14744/TurkPediatriArs.2019.15045  Page 

4.Clinical characteristics of pediatric patients with first-line acute rheumatic fever following the updated guideline
Mühlike Güler, Fuat Laloğlu, Haşim Olgun, Naci Ceviz
doi: 10.14744/TurkPediatriArs.2019.69376  Page 

5.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 

6.Is hepcidin related with anemia and bone mineral metabolism in children with non-dialysis chronic kidney disease?
Osman Yeşilbaş, Nurdan Yıldız, Özgür Baykan, Harika Alpay
doi: 10.14744/TurkPediatriArs.2019.93206  Page 

7.Problem gambling and concurrent emotional/behavioral problems among Greek adolescents
Assimina Paleologou, Helen Lazaratou, Dimitris Anagnostopoulos, Marina Economou, Melpomeni Malliori, George Papadimitriou, Charalampos Papageorgiou
doi: 10.14744/TurkPediatriArs.2019.56254  Page 

REVIEW
8.
Çocuklarda Gastrointestinal Hastalıkların Tanı Ve Takibinde Dışkı İncelemelerinin Yeri
Erhun Kasırga
doi: 10.14744/TurkPediatriArs.2018.00483  Page 

9.
Çocuklarda Obezite Tedavisinde Egzersiz
Selda Bülbül
doi: 10.14744/TurkPediatriArs.2019.60430  Page 

10.Long-term outcome of autism spectrum disorder
Annio Posar, Paola Visconti
doi: 10.14744/TurkPediatriArs.2019.16768  Page 

CASE REPORT
11.Acquired lung cysts in a premature neonate with congenital cytomegalovirus infection
Özdemir Özmert, Ceren Çıralı, Hacer Ergin, Ebru Nevin Çetin, Ateş Kara
doi: 10.14744/TurkPediatriArs.2018.99907  Page 

12.Eosinophilic gastroenteritis as a cause of gastrointestinal system bleeding and protein loosing enteropathy
Makbule Eren, Nujin Uluğ, Yusuf Aydemir
doi: 10.14744/TurkPediatriArs.2018.48276  Page 

13.Rare Cause of Acute Severe Upper Airway Obstruciton Which Required Endotracheal Intubation: Adenoid Hypertrophy
Uğur Yıldırım, Özgür Kemal, Esra Kavaz, Sinan Atmaca, Mehmet Koyuncu
doi: 10.14744/TurkPediatriArs.2018.89156  Page 

14.Septal myectomy and implantable cardiac defibrillator implantation in infant with hypertrophic cardiomyopathy and newly identified MYBPC3 genetic mutation
Osman Güvenç, Kadri Karaer, Sertaç Haydin, Alper Güzeltaş, Yakup Ergül
doi: 10.14744/TurkPediatriArs.2018.35556  Page 

15.
Olgu sunumu: moleküler düzeyde tanısı konulmuş olan ilk Türk Rotor sendromlu aile
Evren Gümüş, Meryem Karaca, Uğur Deveci, Milan Jirsa
doi: 10.14744/TurkPediatriArs.2019.55798  Page 

16.A Case of Classic Galactosemia Manifesting as Neonatal Early and Profound Indirect hyperbilirubinemia
Zohreh Kavehmanesh, Mohammad Torkaman, Fatemeh Beiraghdar
doi: 10.14744/TurkPediatriArs.2019.21298  Page 

17.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 

18.A Novel de novo Mutation at ABCC8 Gene in a Newborn with Transient Diabetes Mellitus
Semih Bolu, İbrahim Hakan Bucak, Çapan Konca, İrem Eldem, Mehmet Tekin
doi: 10.14744/TurkPediatriArs.2019.01336  Page 

19.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 

20.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 

21.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 

22.Clinical characteristics of a Turkish family with congenital erythrocytosis due to EPOR mutation. Is routine phlebotomy indicated in children and adolescents?
Nazan Sarper, Emine Zengin, Sema Aylan Gelen
doi: 10.14744/TurkPediatriArs.2019.65481  Page 

23.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 

24.IgG4 related disease in a 7 year old girl with multiple organ involvement: A rare presentation
Bilge Şahin Akkelle, Engin Tutar, Rabia Ergelen, Çiğdem A. Çelikel, Deniz Ertem
doi: 10.14744/TurkPediatriArs.2019.83435  Page 

25.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: 10.14744/TurkPediatriArs.2019.37232  Page 

26.Primary Ovarian Rhabdomyosarcoma Coexisting with Pseudo-Meigs’ Syndrome in a Young Patient: A Case Report and Brief Literature Review

doi: 10.14744/TurkPediatriArs.2019.82474  Page 

27.Recurrent infections, neurological signs, low serum uric acid levels and lymphopenia in childhood: Purine nucleoside phosphorylase deficiency, an emergency for infants
Necil Kütükçüler, Ezgi Bölük, Nazan Tökmeci, Neslihan Edeer Karaca, Elif Azarsız, Güzide Aksu, Ayça Aykut
doi: 10.14744/TurkPediatriArs.2019.83788  Page 

28.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 

29.Successful outcome of mucormycosis in a child with acute lymphoblastic leukemia
Rejin Kebudi, Hande Kızılocak, Günter Hafız, Zayre Erturan
doi: 10.14744/TurkPediatriArs.2019.12129  Page 

30.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 

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

32.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 

LETTER TO THE EDITOR
33.Drug choice for pediatric procedural sedation-analgesia and adrenaline administration route in anaphylaxis treatment
Osman Yeşilbaş, Selçuk Uzuner
doi: 10.14744/TurkPediatriArs.2018.54926  Page 
Abstract

34.Occurrence of rhabdomyolysis, serotonin syndrome, and acute respiratory distress syndrome in a child secondary to ecstasy intoxication
Osman Yeşilbaş, Selçuk Uzuner, Çiğdem Korkmaz, Lala Nurmammadova, Ayşegül Doğan Demir
doi: 10.14744/TurkPediatriArs.2019.48265  Page 
Abstract

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