2020 Cilt: 62 - Sayı: 1
İÇİNDEKİLER
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
49.4b 16.1b
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