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Journal of Pediatric Neurosciences|June 15, 2018
Neuro-ichthyotic Syndromes: A Case SeriesFaruk Incecık, Ozlem M Herguner, Mehmet N Ozbek, et al.
Annals of Indian Academy of Neurology|December 17, 2013
Multiple sulfatase deficiency: A case series of four childrenFaruk Incecik, Mehmet N Ozbek, Serdal Gungor, et al.
The New England Journal of Medicine|February 17, 2012
Inactivating KISS1 mutation and hypogonadotropic hypogonadismA Kemal Topaloglu, Javier A Tello, L Damla Kotan, et al.
Molecular Biology Reports|April 22, 2019
The molecular basis and genotype-phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian populationAyca Dundar, Ruslan Bayramov, Muge G Onal, et al.
Diabetologia|October 23, 2021
Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinicsKashyap A Patel, Mehmet N Ozbek, Melek Yildiz, et al.
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