Funda F. Tas - Publications

Evaluation of iodine and selenium level and thyroid functions in patients with cystic fibrosis.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: November 26, 2024

Evaluation and management of neonatal onset hyperinsulinemic hypoglycemia: a single neonatal center experience.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians

Published: October 20, 2023

The clinical and laboratory features of patients with triple A syndrome: a single-center experience in Turkey.

Journal: Endocrine

Published: August 05, 2022

Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year

Journal: Journal of clinical research in pediatric endocrinology

Published: June 23, 2022

Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report

Journal: Journal of clinical research in pediatric endocrinology

Published: January 11, 2022

A novel variant in LCHGR gene in 3 siblings with type 1 Leydig cell hypoplasia.

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

Published: July 14, 2020

Identification of four novel variant in the AMHR2 gene in six unrelated Turkish families.

Journal: Journal of endocrinological investigation

Published: July 13, 2020

Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature review.

Journal: Hormones (Athens, Greece)

Published: May 06, 2020

A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in CYP17A1 gene.

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

Published: December 31, 2019

Aromatase Deficiency due to a Novel Mutation in CYP19A1 Gene

Journal: Journal of clinical research in pediatric endocrinology

Published: March 20, 2018

A rare cause of neonatal hypoglycemia in two siblings: TBX19 gene mutation.

Journal: Hormones (Athens, Greece)

Published: December 26, 2017

Unusual cause of hyperammonemia in two cases with short-term and long-term valproate therapy successfully treated by single dose carglumic acid.

Journal: Journal of pediatric neurosciences

Published: January 29, 2014