Multigene Panel Testing in Turkish Hereditary Cancer Syndrome Patients

por ARSLAN ATES, Esra, TURKYILMAZ, Ayberk, ALAVANDA, Ceren, YILDIRIM, Ozlem, GUNEY, Ahmet Ilter
Publicado 2022

miR-34a-FOXP1 Loop in Ovarian Cancer

por Dirimtekin, Esra, Mortoglou, Maria, Alavanda, Ceren, Benomar Yemlahi, Asmaa, Arslan Ates, Esra, Guney, Ilter, Uysal-Onganer, Pinar
Publicado 2023

Molecular Aspects of Distal Kidney Tubular Acidosis in Children, Its Long-Term Outcome, and Relationship with Hyperammonemia

por Güven, Serçin, Gökçe, İbrahim, Alavanda, Ceren, Öztürk Hişmi, Burcu, Çiçek, Neslihan, Bodur Demirci, Ece, Sak, Mehtap, Yıldız, Nurdan, Ata, Pınar, Alpay, Harika
Publicado 2022

Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity

por Turan, Serap, Mumm, Steven, Alavanda, Ceren, Kaygusuz, Betul Sare, Gurpinar Tosun, Busra, Arman, Ahmet, Huskey, Margaret, Guran, Tulay, Duan, Shenghui, Bereket, Abdullah, Whyte, Michael P.
Publicado 2022

A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age

por Eltan, Mehmet, Alavanda, Ceren, Yavas Abali, Zehra, Ergenekon, Pinar, Yalındag Ozturk, Nilufer, Sakar, Mustafa, Dagcinar, Adnan, Kirkgoz, Tarik, Kaygusuz, Sare Betul, Gokdemir, Yasemin, Elcioglu, Huriye Nursel, Guran, Tulay, Bereket, Abdullah, Ata, Pinar, Turan, Serap
Publicado 2020