Yazar "Nikerel, Emrah" için listeleme
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Clinical, demographic and genetic features of patients with congenital heart disease : A single center experience
Kaymakcalan, Hande; Yalcinkaya, Leyla; Nikerel, Emrah; Yalcin, Yalim; Dong, Weilai; Sencicek, Adife Gulhan Ercan (Marmara Univ, Fac Medicine, 2022)Objective: We aimed to evaluate the demographic and clinical characteristics of children with congenital heart disease (CHD) in a private pediatric cardiovascular genetics clinic in Istanbul from January 2016 to July 2018 ... -
Prevalence and clinical/molecular characteristics of PTEN mutations in Turkish children with autism spectrum disorders and macrocephaly
Kaymakcalan, Hande; Kaya, Ilyas; Binici, Nagihan Cevher; Nikerel, Emrah; Ozbaran, Burcu; Aksoy, Mehmet Gorkem; Erbilgin, Seda (Wiley, 2021)Background: Phosphatase and tensin homolog (PTEN) germline mutations are associated with cancer syndromes (PTEN hamartoma tumor syndrome; PHTS) and in pediatric patients with autism spectrum disorder (ASD) and macrocephaly. ...