Funda Feryal Taş (Funda Taş, F F Taş)

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 6

Top Topics

Pulmonary Embolism

Genome Wide Identification

Intellectual Disability

Top Venues

Journal of clinical research in pediatric endocrinology

Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology

Journal of endocrinological investigation

This page only lists publications with an associated author ORCID identifier.

Publications

Şervan Özalkak, Ruken Yıldırım, Selma Tunç, Edip Unal, Funda Feryal Taş, Hüseyin Demirbilek, Mehmet Nuri Özbek
Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report Journal of clinical research in pediatric endocrinology 14 (2) (2022)
Ruken Yıldırım, Edip Unal, Aysel Tekmenuray-Unal, Funda Feryal Taş, Şervan Özalkak, Atilla Çayır, Mehmet Nuri Özbek
The clinical and laboratory features of patients with triple A syndrome: a single-center experience in Turkey. Endocrine (2022)
Edip Unal, Meliha Demiral, Ruken Yıldırım, Funda Feryal Taş, Serdar Ceylaner, Mehmet Nuri Özbek
Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature review. Hormones (Athens, Greece) 20 (2) (2020)
Edip Unal, Amine Aktar Karakaya, Aslı Beştaş, Ruken Yıldırım, Funda Feryal Taş, Hüseyin Onay, Ferda Özkınay, Yusuf Kenan Haspolat
Identification of four novel variant in the AMHR2 gene in six unrelated Turkish families. Journal of endocrinological investigation 44 (6) (2020)
Amine Aktar Karakaya, Edip Unal, Aslı Beştaş, Funda Feryal Taş, Hüseyin Onay, Yusuf Kenan Haspolat
A novel variant in LCHGR gene in 3 siblings with type 1 Leydig cell hypoplasia. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 36 (12) (2020)
Edip Unal, Ruken Yıldırım, Funda Feryal Taş, Vasfiye Demir, Hüseyin Onay, Yusuf Kenan Haspolat
Aromatase Deficiency due to a Novel Mutation in CYP19A1 Gene Journal of clinical research in pediatric endocrinology 10 (4) (2018)