A mother and son with Noonan syndrome resulting from a PTPN11 mutation by Murat Derbent

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Severe iron deficiency anemia in a child with idiopathic pulmonary hemosiderosis: a case report by Murat Derbent, Figen Ozçay, Umit Saatçi, Namik Ozbek

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Tetralogy of Fallot and hypertrophic cardiomyopathy in a case of cardiofaciocutaneous syndrome by Selman Vefa Yildirim, Eren Kale-Cekinmez, Deren Ozcan, Murat Derbent

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A case of Mowat-Wilson syndrome caused by a truncating mutation within exon 8 of the ZEB2 gene by Cihan Meral, Bariy Malbora, Fatih Celikel, Gökhan Aydemir, Selami Süleymanoğlu, Marcella Zollino, Murat Derbent

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Propranolol for infantile hemangiomas: a preliminary report on efficacy and safety in very low birth weight infants by Ayşe Erbay, Faik Sarialioglu, Bariş Malbora, Selman Vefa Yildirim, Birgül Varan, Aylin Tarcan, Hande Gülcan, Senay Demir, Murat Derbent, Nihal Uslu, Aslihan Abbasoğlu

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MOWAT-WILSON SYNDROME: DEEP PHENOTYPING AND MOLECULAR CHARACTERISATION OF TWELVE NEW INDIVIDUALS by Umut Altunoğlu, Nilay Güneş, Gözde Tutku Turgut, Tuğba Kalaycı, Ayça Dilruba Aslanger, Murat Derbent, Serpil Eraslan, Birsen Karaman, Zehra Oya Uyguner, Beyhan Tüysüz, Yasemin Alanay, Hülya Kayserili Karabey

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Outcome of out-of-hospital cardiopulmonary arrest in children: A multicenter cohort study by Funda Kurt, Benan Bayrakcı, Özlem Tekşam, Deniz Tekin, Okşan Derinöz, Emine Polat, Sinan Oğuz, Ayşe Gültekingil, Çağlar Ödek, Nilden Tuygun, Murat Derbent, Gökhan Kalkan, Şanlıay Şahin, Halise Akça, Selman Kesici, Ramiz Coskun Gündüz, Tanıl Kendirli, Emine Suskan

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