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Hormone Research in Paediatrics|November 4, 2024
Clinical and Genetic Mechanisms in Patients with MC2R Deficiency Presenting with Early PubertyEsin Karakilic Ozturan, Zehra Yavas Abali, Volkan Karaman, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|December 5, 2013
Evaluation of endocrine function in children admitted to pediatric intensive care unitBanu Küçükemre Aydın, Demet Demirkol, Firdevs Baş, et al.Journal of Pediatric Orthopedics|June 4, 2008
Successful results of pamidronate treatment in children with osteogenesis imperfecta with emphasis on the interpretation of bone mineral density for local standardsSukran Poyrazoglu, Hulya Gunoz, Feyza Darendeliler, et al.Journal of Clinical Research in Pediatric Endocrinology|February 9, 2022
Comparison of National Growth Standards for Turkish Infants and Children with World Health Organization Growth StandardsRüveyde Bundak, Zehra Yavaş Abalı, Andrzej Furman, et al.Clinical Endocrinology|December 17, 2021
Pelvic and breast ultrasound abnormalities and associated metabolic disturbances in girls with premature pubarche due to adrenarcheBanu K Aydin, Alev Kadioglu, Gamze A Kaya, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2004
Reevaluation of growth hormone deficiency during and after growth hormone (GH) treatment: diagnostic value of GH tests and IGF-I and IGFBP-3 measurementsFeyza Darendeliler, Isabel Spinu, Firdevs Bas, et al.Endocrine Research|October 21, 2014
A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defectHakan Cangul, Feyza Darendeliler, Yaman Saglam, et al.Journal of the Endocrine Society|May 30, 2019
Frequency of Ambiguous Genitalia in 14,177 Newborns in TurkeyBanu Kucukemre Aydin, Nurcin Saka, Firdevs Bas, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|August 30, 2002
ABCC8 (SUR1) and KCNJ11 (KIR6.2) mutations in persistent hyperinsulinemic hypoglycemia of infancy and evaluation of different therapeutic measuresFeyza Darendeliler, Jean-Christophe Fournet, Firdevs Baş, et al.Hormones (Athens, Greece)|November 22, 2018
Precocious or early puberty in patients with combined pituitary hormone deficiency due to POU1F1 gene mutation: case report and review of possible mechanismsFirdevs Baş, Zehra Yavaş Abalı, Güven Toksoy, et al.Pageof 20