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Journal of Clinical Research in Pediatric Endocrinology|December 24, 2016
Association of Subclinical Hypothyroidism with Dyslipidemia and Increased Carotid Intima-Media Thickness in ChildrenEdip Unal, Alper Akın, Ruken Yıldırım, et al.Journal of Clinical Research in Pediatric Endocrinology|April 25, 2018
A Novel Mutation of <i>AMHR2</i> in Two Siblings with Persistent Müllerian Duct SyndromeEdip Unal, Ruken Yıldırım, Suat Tekin, et al.Journal of Clinical Research in Pediatric Endocrinology|January 29, 2020
Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital HypothyroidismMuhammet Asena, Meliha Demiral, Edip Unal, et al.Sisli Etfal Hastanesi Tip Bulteni|October 16, 2024
Evaluation of Oral Glucose Tolerance Test Results in Children with Cystic FibrosisAsli Bestas, Edip Unal, Amine Aktar Karakaya, et al.Pacing and Clinical Electrophysiology : PACE|January 26, 2018
Evaluation of QT dispersion and Tp-e interval in children with subclinical hypothyroidismAlper Akın, Edip Unal, Ruken Yıldırım, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|June 17, 2024
Retrospective evaluation of patients diagnosed with central precocious puberty who reached the final heightKadri Yaman, Edip Unal, Aslı Beştaş, et al.Journal of Clinical Research in Pediatric Endocrinology|November 30, 2019
Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the <i>GLI2</i> GeneMeliha Demiral, Hüseyin Demirbilek, Edip Unal, et al.Journal of Clinical Research in Pediatric Endocrinology|March 20, 2018
Aromatase Deficiency due to a Novel Mutation in <i>CYP19A1</i> GeneEdip Unal, Ruken Yıldırım, Funda Feryal Taş, et al.Journal of Clinical Research in Pediatric Endocrinology|March 12, 2020
Evaluation of the Final Adult Height and Its Determinants in Patients with Growth Hormone Deficiency: A Single-centre Experience from the South-Eastern Region of TurkeyMeliha Demiral, Edip Unal, Birsen Baysal, et al.Hormones (Athens, Greece)|October 30, 2020
Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature reviewEdip Unal, Meliha Demiral, Ruken Yıldırım, et al.Pageof 5