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Pediatric Nephrology (Berlin, Germany)|May 21, 2024
Association of problems, coping styles, and preferred online activity with depression, anxiety, and other psychological disorders in Turkish adolescents diagnosed with chronic kidney diseaseIbrahim Kandemir, Kemal Gudek, Aylin Yetim Sahin, et al.Journal of Clinical Research in Pediatric Endocrinology|March 29, 2023
Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in TurkeyEsin Karakılıç Özturan, Ayşe Pınar Öztürk, Firdevs Baş, et al.Journal of Clinical Research in Pediatric Endocrinology|January 29, 2011
CYP21A2 gene mutations in congenital adrenal hyperplasia: genotype-phenotype correlation in Turkish childrenFirdevs Baş, Hülya Kayserili, Feyza Darendeliler, et al.Pediatric Research|January 11, 2007
Major determinants of height development in Turner syndrome (TS) patients treated with GH: analysis of 987 patients from KIGSMichael B Ranke, Anders Lindberg, Angel Ferrández Longás, et al.Journal of Clinical Research in Pediatric Endocrinology|February 9, 2022
Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSDNeşe Akcan, Oya Uyguner, Firdevs Baş, et al.Journal of Clinical Research in Pediatric Endocrinology|October 10, 2024
Gonadoblastoma with Dysgerminoma in a Virilized Adolescent with Karyotype 46,XX: A Case Report and Review of the LiteratureTuğçe Kandemir, Esin Karakilic Ozturan, Özlem Dural, et al.Omics : a Journal of Integrative Biology|June 26, 2021
Monogenic Childhood Diabetes: Dissecting Clinical Heterogeneity by Next-Generation Sequencing in Maturity-Onset Diabetes of the YoungDeniz Kanca Demirci, Feyza Darendeliler, Sukran Poyrazoglu, et al.The Journal of Steroid Biochemistry and Molecular Biology|April 8, 2018
Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 geneFirdevs Baş, Güven Toksoy, Berrin Ergun-Longmire, et al.The Journal of Clinical Endocrinology and Metabolism|May 2, 2019
Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of DiseaseAngad Jolly, Yavuz Bayram, Serap Turan, et al.Journal of Clinical Research in Pediatric Endocrinology|July 14, 2011
Serum IGF-1 and IGFBP-3 levels in healthy children between 0 and 6 years of ageBilgin Yüksel, M Nuri Özbek, Neslihan Önenli Mungan, et al.Pageof 22