Invasive fungal infection in children with hematologic malignancy

Belgin GÜLHAN, Saliha Kanık YÜKSEK, Aslınur Özkaya PARLAKAY, Neşe YARALI, Hasan TEZER, Namık Yaşar ÖZBEK

Tocilizumab treatment in juvenile idiopathic arthritis patients: A single center experience

Selcan DEMİR, Hafize Emine SÖNMEZ, Elif Arslanoğlu AYDIN, Seza ÖZEN, Yelda BİLGİNER

Renal features of Bardet Biedl syndrome: A single center experience

Bahriye ATMIŞ, Aysun Karabay BAYAZIT, Engin MELEK, Atıl BİŞGİN, Ali ANARAT

Detection and molecular characterization of uncommon rotavirus group A genotype G12 among hospitalized children in Chennai

Ponnambalam ARUN, Kaveri KRİSHNASAMİ, Palani GUNASEKERAN, Gracy FATHİMA, Vidya PADMANABHAN

Evaluation of growth in children and adolescents after renal transplantation

Bahar BÜYÜKKARAGÖZ, Sevcan Azime BAKKALOĞLU, Ayşe Fitnat TUNCEL, Banu Kadıoğlu YILMAZ, Deniz KARCAALTINCABA, Hatice PAŞAOĞLU

A novel de novo KCNQ2 mutation in a child with treatmentresistant early-onset epileptic encephalopathy

Christina BENETOU, Stavroula PAPAİLİOU, Despoina MARİTSİ, Katherine ANAGNOSTOPOULOU, Harry KONTOS, Georgios VARTZELİS

Alpha methyl acyl CoA racemase deficiency: Diagnosis with isolated elevated liver enzymes

Mehmet GÜNDÜZ, Özlem ÜNAL, Aynur Küçükçongar YAVAŞ, Çiğdem KASAPKARA

Fetal intrapericardial teratomas

Shi Min YUAN, Hong LİN

Comparison of i-gel, LMA-supreme, LMA-classic and LMAproseal as conduits of endotracheal intubation in newborns and infants: A manikin study

Aysun Ankay YILBAŞ, Betül BAŞARAN, Filiz ÜZÜMCÜGİL, Başak AKÇA, Murat İZGİ, Özgür CANBAY

The relationship between prenatal testosterone and developmental stuttering in boys

Yunus Emre DÖNMEZ, Özlem ÖZCAN, Ayhan BİLGİÇ, Dilşad Yıldız MİNİKSAR

Cigarette smoking in adolescents with type 1 diabetes mellitus and congenital adrenal hyperplasia

Pelin ASFUROĞLU, Aslıhan Araslı YILMAZ, Zehra AYCAN

The impact of 21-hydroxylase deficiency on cardiac repolarization changes in children with 21-hydroxylasedeficient congenital adrenal hyperplasia

Hüseyin Anıl KORKMAZ, Rahmi ÖZDEMİR, Mehmet KÜÇÜK, Cem KARADENİZ, Timur MEŞE, Behzat ÖZKAN

Clinical signs and symptoms of toxic serum digoxin levels in neonates

Mehmet MUTLU, Yakup ASLAN, Şebnem KADER, Filiz Aktürk ACAR, Embiya DİLBER

A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome

Işık Odaman AL, Alper GEZDİRİCİ, Melek YILDIZ, Gizem ERSOY, Gönül AYDOĞAN, Zafer SALCIOĞLU, Tuba Nur TAHTAKESEN, Hasan ÖNAL, Banu Küçükemre AYDIN

Neonatal form of biotin-thiamine-responsive basal ganglia disease. Clues to diagnosis

Aydan DEĞERLİYURT, Mehmet GÜNDÜZ, Serdar CEYLANER, Özlem ÜNAL

Bismuth intoxication resulting in acute kidney injury in a pregnant adolescent girl

Aslı Çelebi TAYFUR, Raziye Merve YARADILMIŞ, Fatma ULUS, Aysun Çaltık YILMAZ, Esra ÖZAYAR, Berrin KOŞAR, Bahar BÜYÜKKARAGÖZ, Eyüp HORASANLI

Clinical, electrophysiological findings and evaluation of prognosis of patients with Guillain-Barré syndrome

Betül KILIÇ, Serdal GÜNGÖR, Bilge ÖZGÖR

Comparison of diastolic function in children with transfusion dependent beta thalassemia major by tissue and conventional doppler imaging indices and its correlation with serum ferritin levels

Chetan Kumar NANJEGOWDA, Sowmini Padmanabh KAMATH, Padmanabh KAMATH, Tejas Dushyantbhai SHAH, Vaman KULKARNİ, Harsha Prasada LASHKARİ, Bantwal Shantharam BALİGA

First report of human ehrlichiosis in Turkey

Melike EMİROĞLU, Bekir ÇELEBİ

A rare chromosomal disorder in a newborn: Trisomy 3q

Dilek KAHVECİOĞLU, Hatice Tatar AKSOY, Eren YILDIZ, Abdullatif BAKIR, Bülent ALİOĞLU

Giant axonal neuropathy: A differential diagnosis of consideration

Pınar EDEM, Mert KARAKAYA, Brunhilde WİRTH, Tuncay Derya OKUR, Uluç YİŞ

An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment

Çiğdem Seher KASAPKARA, Ebru Yılmaz KESKİN, Ferda Özbay HOŞNUT, Meltem AKÇABOY, Emine POLAT, Asburçe OLGAÇ, Pelin ZORLU

Self-introduced intravesical magnets in a 3-year-old boy: Case report

Tunç ÖZDEMİR, Gizem ORHAN, Belce CANDAN, Gökhan KÖYLÜOĞLU

Hemophagocytic lymphohistiocytosis associated with oxcarbazepine

Serkan KIRIK, Hatice GÜNEŞ, Sadık YURTTUTAN, Nafiz SARIŞIK, Can ACIPAYAM, Yasemin KIRIK

Kawasaki disease complicated by peripheral gangrene and a ventricular septal defect: An unusual association

Muhammad MOHSİN, Saleem AKHTAR

Noninvasive respiratory support via nasal cannula in premature infants: Is it really safe?

Mehmet BÜYÜKTİRYAKİ, Nilüfer OKUR, Gülsüm Kadıoğlu ŞİMŞEK, Hayriye Gözde KANMAZ, Fuat Emre CANPOLAT

Etiology of vaginal discharge in sexually inactive adolescents

Yasemin DÜZÇEKER, Sinem AKGÜL, Yasemin ÖZSÜREKÇİ, Orhan DERMAN, Ateş KARA, Nuray KANBUR

Priapism: A rare presentation of precursor B-Cell acute lymphoblastic leukemia

Zeliha GÜZELKÜÇÜK, Dilek KAÇAR, Rabia DEMİR, Meltem KÜRTÜL, Hüsniye Neşe YARALI, Namık Yaşar ÖZBEK

Clinical findings and genetic analysis of the patients with IL-12Rβ1 deficiency from southeast Turkey

Derya Alabaz, Derya Ufuk Altıntaş, Dilek Doğruel, Emine Kocabaş, Mustafa Yılmaz, Özlem Özgür Gündeşlioğlu