Foot hexadactyly, social implications and management in the African setting: Case report
Komla Sena Amouzou, Elodie Lucrece Joyce Malonga-Loukoula, Tete Edem Kouevi-Koko, Batarabadja Bakriga, Anani Abalo
A rare cause of facial nerve palsy in a young infant: Kawasaki disease
Ali ORGUN, Cüneyt KARAGÖL, Utku PAMUK, Hazım Alper GÜRSU, İlker ÇETİN
Chylous ascites after lymphadenectomy in a Wilms’ tumor patient
Mustafa Asım YÖRÜK, Meryem ERAT NERGİZ, Çetin TİMUR, AYLİN CANBOLAT AYHAN, Müferet ERGÜVEN
Autism spectrum disorder and beta thalassemia minor: A genetic link?
Venous thromboembolism in two adolescents with Down syndrome
Kei Takasawa, Masato Nishioka, Masayuki Shimohira, Reiko Takasawa, Sayaka Takeda, Masashi Kurobe, Tsunehiko Kurokami
Apolipoprotein E allelic variants and cerebral palsy
Evren GÜMÜŞ, Beyhan DURAK ARAS, Oğuz ÇİLİNGİR, Coşkun YARAR, Kürşat Bora ÇARMAN, Sibel LAÇİNER GÜRLEVİK, Ozan KOÇAK, Sevilhan ARTAN
Is the BCS1L variant c.232A>G truly responsible for a GRACILE-like condition?
Josef FINSTERER, Sinda Zarrouk MAHJOUB
The association between monosymptomatic enuresis and allergic diseases in children
Caner Alparslan, Demet Alaygut, Suzan Yılmaz Durmuş, Seda Şirin Köse, Özden Anal, Alper Soylu
Changes of primary headache related white matter lesions in pediatric patients
Erhan BAYRAM, Uluç YİŞ, Cem PAKETÇİ, Derya OKUR, İpek POLAT, Handan ÇAKMAKÇI, Semra HIZ, Banu ANLAR
Helen Aghdasi BORNAUN, Günsel KUTLUK, Gonca KESKİNDEMİRCİ, Kazım ÖZTARHAN, Reyhan DEDEOĞLU, Nuh YILMAZ, Öykü TOSUN