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Journal of Pediatric Endocrinology & Metabolism : JPEM|April 21, 2021
Different clinical entities of the same mutation: a case report of three sisters with Wolfram syndrome and efficacy of dipeptidyl peptidase-4 inhibitor therapyGurkan Tarcin, Hande Turan, Aydilek Dagdeviren Cakir, et al.Pediatric Hematology and Oncology|October 4, 2013
The effect of HFE polymorphisms on cardiac iron overload in patients with beta-thalassemia majorAysen Turedi, Yesim Oymak, Timur Meşe, et al.Fetal Diagnosis and Therapy|February 10, 2009
Prenatally diagnosed Turner syndrome and cystic hygroma: incidence and reasons for referralsAsude Alpman, Ozgur Cogulu, Mehmet Akgul, et al.Clinical Dysmorphology|June 22, 2011
Homozygous mutation of CRLF-1 gene in a Turkish newborn with Crisponi syndromeHese Cosar, Zelal Kahramaner, Aydin Erdemir, et al.Journal of Genetic Counseling|January 12, 2011
Reasons for adult referrals for genetic counseling at a genetics center in Izmir, Turkey: analysis of 8965 cases over an eleven-year periodOzgur Cogulu, Ferda Ozkinay, Haluk Akin, et al.Neuropediatrics|December 26, 2025
EVALUATION OF EXPERIENCED CLINICAL EVENTS IN POMPE DISEASE BASED ON REAL-LIFE DATAFehime Erdem Karapınar, Havva Yazıcı, Merve Yoldaş Çelik, et al.Annals of Medicine|April 26, 2007
Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depressionTimo Partonen, Jens Treutlein, Asude Alpman, et al.Pageof 2