A novel Y160C mutation of Keratin 10 gene in a Chinese male infant with epidermolytic hyperkeratosis
Chenyu ZHAO, Yonggui LI, Gaoxing SHI, Xiaoliu SHI, Guiying ZHANG
Perfusion index and pleth variability index in the first hour of life according to mode of delivery
Şule YİĞİT, Şahin TAKÇI, Davut BOZKAYA, Murat YURDAKÖK
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
Changes in trajectories of physical growth in a domestic adoptees sample: A preliminary study
Pietro FERRARA, Costanza CUTRONA, Chiara GUADAGNO, Maria Elisa AMODEO, Ester Del VESCOVO, Francesca IANNİELLO, Tommasangelo PETİTTİ
Helen Aghdasi BORNAUN, Günsel KUTLUK, Gonca KESKİNDEMİRCİ, Kazım ÖZTARHAN, Reyhan DEDEOĞLU, Nuh YILMAZ, Öykü TOSUN
Venous thromboembolism in two adolescents with Down syndrome
Kei Takasawa, Masato Nishioka, Masayuki Shimohira, Reiko Takasawa, Sayaka Takeda, Masashi Kurobe, Tsunehiko Kurokami
An asthmatic child with allergic bronchopulmonary aspergillosis (ABPA)
A rare cause of facial nerve palsy in a young infant: Kawasaki disease
Ali ORGUN, Cüneyt KARAGÖL, Utku PAMUK, Hazım Alper GÜRSU, İlker ÇETİN
Response to ''Is the BCS1L variant c.232A>G truly responsible for a GRACILE-like condition?''
Şahin Takcı, Şule Yiğit, Esra Serdaroğlu, Vineta Fellman
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