2019 Cilt: 61 - Sayı: 2
İÇİNDEKİLER
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
47.5b 13.1b
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