Risk factors of intravenous immunoglobulin resistance and coronary arterial lesions in Turkish children with Kawasaki disease

Serkan TÜRKUÇAR, Kaan YILDIZ, Ceyhun ACARI, Hatice ADIGÜZEL DUNDAR, Mustafa Çağlar KIR, Erbil ÜNSAL

Cord blood delta neutrophil index values of term neonates

Melek BÜYÜKEREN, Hasan Tolga ÇELİK, Oytun PORTAKAL, Erdem FADILOĞLU, Gökçen ÖRGÜL, Şule YİĞİT, M. Sinan BEKSAÇ, Murat YURDAKÖK

Infection risk after paediatric liver transplantation

Mukadder Ayşe SELİMOĞLU, Samime KAYA, RECEP ŞÜKRÜ GÜNGÖR, Fatma İlknur VAROL, Harika Gözde GÖZÜKARA BAĞ, Sezai YILMAZ

Assessment of motor development using the Alberta Infant Motor Scale in full-term infants

Büşra KEPENEK VAROL, Zeynep HOŞBAY, Hüseyin Selçuk VAROL, Emel TORUN

A novel homozygous nonsense mutation (p.Y78*) in TMPRSS6 gene causing iron-refractory iron deficiency anemia (IRIDA) in two siblings

Seda ÇAKMAKLI, Çiğdem BUĞAN KAPLAN, Mehmet UZUNOĞLU, Merve BÜYÜKBAYRAM, Emel GÖRGÜLÜ, Nurten ÖZKAN ZARİF, Ebru KESKİN

Early-onset neonatal sepsis caused by Neisseria meningitidisserogroup B: case report and literature review of a 102-year period

Tayyib MUBASHAR, Paul Christopher TURNER, Siba Prosad PAUL

Dropped head related lamin A/C associated congenital muscular dystrophy case; previously defined as emery-dreifuss muscular dystrophy

Hande GAZATECİ TEKİN, Sabire Sanem YILMAZ, Hasan TEKGÜL, Sarenur GÖKBEN, Gül AKTAN

Obstructive jaundice and severe pancreatitis due to the foramen of Winslow hernia with multiple anomalies

Neslihan EKŞİ BOZBULUT, İsmail AKDULUM, Ahmet Sinan SARI, İbrahim Onur ÖZEN, Yusuf Hakan ÇAVUŞOĞLU, Öznur BOYUNAĞA, DALGIÇ Aydın, Buket DALGIÇ

A rare cause of acute abdominal pain in a patient with Primary ciliary dyskinesia with situs inversus totalis

Kısmet ÇIKI, Özlem Boybeyi TÜRER, Mina Gharibzadeh HIZAL, Gökçen Dilşa TUĞCU, Nagehan EMİRALİOĞLU, Ebru ŞAHİN YALÇIN, Deniz DOĞRU ERSÖZ, Nural KİPER, Uğur ÖZÇELİK

Gross motor development of preschool children: effects of socioeconomic status and maternal education

Cemil ÖZAL, Birgül BAYOĞLU, Sevilay KARAHAN, Kerem Mintaze GÜNEL, Fatma Banu ANLAR

Detection of allele frequencies of common c. 511C>T and c.625G>A variants in the ACADS gene in the Turkish population

Mustafa KILIÇ, Bekir ERGÜNER, Can KOŞUKÇU, Rıza Köksal ÖZGÜL

Clinical and laboratory predictors of survival for pediatric patients on non-postcardiotomy extracorporeal membrane oxygenation (ECMO)

Güntülü ŞIK, Asuman DEMİRBUĞA, Agageldi ANNAYEV, Bahar TEMUR, Yavuz Selim AYDIN, Halil İbrahim DEMİR, Ersin EREK, Agop ÇITAK

Evaluation of pentraxin 3 level and cardiac functions in psoriatic children

Mecnun ÇETİN, İbrahim Halil YAVUZ, Göknur ÖZAYDIN YAVUZ, Kamuran KARAMAN

Mother-child interaction and the development status of children who have been accidentally poisoned

Ganime AYAR, Tülin KÖKSAL, Funda VURAL KURT, Aysun KARA UZUN, Bahar ÇUHACI ÇAKIR, Birgül BAYOĞLU, Sıddıka Songül YALÇIN

Factors affecting the success of pediatric extracorporeal shock wave lithotripsy therapy: 26-year experience at a single institution

FUAT KIZILAY, Turan Senem ÖZDEMİR, Burak TURNA, Nursen KARACA, Adnan ŞİMŞİR, Işık ALPER, Oktay NAZLI

Grisel’s syndrome presenting with neck pain: an atypical case

Emre BİLGİN, Gökhan ÇAVUŞ, Vedat AÇIK, Yurdal GEZERCAN, Ali İhsan ÖKTEN

A rare presentation of adrenal adenoma in infancy: isolated Cushing’s syndrome

Oğuzhan ŞAL, Gülçin YEĞEN, Pelin OĞUZKURT

Children with extreme hyperferritinemia are at risk of receiving more chemotherapy than necessary

Seung Beom HAN, Soo-Young LEE

Red blood cell variables and correlations with body mass components in boys aged 10-17 years

Jasmina Pluncevic GLIGOROSKA, Serjoza GONTAREV, Vesela MALESKA, Ljudmila EFREMOVA, Daniela Shukova STOJMANOVA, Sanja MANCHEVSKA

Cardiorespiratory parameters in newborns during sedation with chloral hydrate

Petja FISTER, Jerneja PECEK, Barbara Gnidovec STRAZISAR, Darja PARO-PANJAN

Are general movements at 3-5 months correlated and compatible with the Bayley-III at 1,5-2 years age?

Aysu KAHRAMAN, Ayşe LİVANELİOĞLU, Özgün Kaya KARA, Murat YURDAKÖK

A rare cause of epileptic encephalopathy: a beta-propeller protein associated neurodegeneration case with a new mutation and literature review

Nezir ÖZGÜN, Leyla ÖZER, Ahmet YARAMIŞ

Novel mutation and severe respiratory failure in congenital disorders of glycosylation Type Ix

Betül KILIÇ, Nejmiye AKKUŞ

Rotavirus encephalopathy with concomitant acute cerebellitis: report of a case and review of the literature

Cem PAKETÇİ, Pınar EDEM, Derya OKUR, Fatma Ceren SARIOĞLU, Handan GÜLERYÜZ, Erhan BAYRAM, Semra Hız KURUL, Uluç YİŞ

Peters Plus syndrome: a recognizable clinical entity

Gizem ÜREL DEMİR, Naz Güleray LAFCI, Özlem AKGÜN DOĞAN, Pelin Özlem ŞİMŞEK KİPER, Gülen Eda UTİNE

Neonatal iliopsoas abscess presenting with transient cyanosis of a single extremity: a case report and review of the literature

Mustafa Şenol AKIN, Damla AĞAÇKIRAN, Hasan Emre ÜNAL, Özlem Özkale YAVUZ, Şule YİĞİT