Nursel Muratoğlu Şahin

Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

Zehra Aycan, Şenay Savaş Erdeve, Semra Çeti̇nkaya et al. · Journal of Clinical Research in Pediatric Endocrinology · 2018 · 27 citations · Full text

Clinical and genetic characterisation of a series of patients with triple A syndrome

Erdal Kurnaz, Paolo Duminuco, Zehra Aycan et al. · European Journal of Pediatrics · 2017 · 26 citations

Down Syndrome, Genetic Characterisation, Mendelian Disorder +8

Comparison of pressure and volume‐controlled ventilation in laparoscopic cholecystectomy operations

Venera Aydın, Hanife Karakaya Kabukçu, Nursel Muratoğlu Şahin et al. · The Clinical Respiratory Journal · 2014 · 24 citations · Full text

A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene

Melikşah Keskın, Nursel Muratoğlu Şahin, Erdal Kurnaz et al. · Journal of Clinical Research in Pediatric Endocrinology · 2016 · 24 citations · Full text

AMH levels at central precocious puberty and premature thelarche: is it a parameter?

Nursel Muratoğlu Şahin, Sibel Tulgar Kınık, Mustafa Agâh Tekindal et al. · Journal of Pediatric Endocrinology and Metabolism · 2015 · 18 citations