Zehra Yavaş Abalı

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

Tülay Güran, Federica Buonocore, Nurçin Saka et al. · The Journal of Clinical Endocrinology & Metabolism · 2015 · 208 citations · Full text

Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease

Angad Jolly, Yavuz Bayram, Serap Turan et al. · The Journal of Clinical Endocrinology & Metabolism · 2019 · 75 citations · Full text

Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency

Erdal Kurnaz, Emine Kartal Baykan, Ayberk Türkyılmaz et al. · Hormone Research in Paediatrics · 2020 · 40 citations

Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency

Zehra Yavaş Abalı, Mehmet Keskın, Mehmet Nuri Özbek et al. · The Journal of Clinical Endocrinology & Metabolism · 2021 · 40 citations · Full text

A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations

Aslı Derya Kardelen, Güven Toksoy, Firdevs Baş et al. · Journal of Clinical Research in Pediatric Endocrinology · 2018 · 37 citations · Full text