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Journal of Clinical Research in Pediatric Endocrinology|March 16, 2026
Early Childhood Obesity: Multifactorial Influences with a Prominent Familial Contributionİsmail Hakkı Akbeyaz, Yasemin Akın, Berkin Berk Akbeyaz, et al.Journal of Clinical Research in Pediatric Endocrinology|February 26, 2026
Mucocutaneous Findings and Endocrinopathies in Children with Turner Syndrome: A Cross-Sectional StudySelami Aykut Temiz, Filiz Cebeci, Aslıhan Çiçekli, et al.Journal of Clinical Research in Pediatric Endocrinology|February 26, 2024
Novel OBSL1 Variant in a Chinese Patient with 3M Syndrome: The c.458dupG Mutation May Be a Potential Hotspot Mutation in the Chinese PopulationYurong Piao, Rongmin Li, Yingjie Wang, et al.Journal of Clinical Research in Pediatric Endocrinology|August 10, 2023
Association of Vitamin D Deficiency and Vitamin D Receptor Gene Polymorphisms with Type 1 Diabetes Risk: A South Indian Familial StudyRamasamy Thirunavukkarasu, Ayyappan Chitra, Arthur Asirvatham, et al.Journal of Clinical Research in Pediatric Endocrinology|April 29, 2024
Predictors and Trends of Diabetic Ketoacidosis at Diagnosis of Type 1 Diabetes Mellitus in Malaysian ChildrenMeenal Mavinkurve, Nurul Hanis Ramzi, Muhammad Yazid Bin Jalaludin, et al.Journal of Clinical Research in Pediatric Endocrinology|September 8, 2023
Novel Variant of SLC34A3 in a Compound Heterozygous Brazilian Girl with Hereditary Hypophosphatemic Rickets with HypercalciuriaLuciana Pinto Valadares, Daniel Rocha de CarvalhoJournal of Clinical Research in Pediatric Endocrinology|April 14, 2026
A 13-Year-Old Girl with Congenital Hyperinsulinemic Hypoglycemia Due to an ABCC8 Mutation and Recent Onset of Diabetes Mellitus: A Case Report and Literature ReviewAikaterini Kantzavelou, Ekaterini Siomou, Anny Mertzanian, et al.Journal of Clinical Research in Pediatric Endocrinology|June 16, 2026
An Unexpected Result in a Case of Gonadal Dysgenesis: Noonan Syndrome Caused by RIT1 MutationŞafak Demirtaş, Elif Özsu, Zeynep Şıklar, et al.Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 DeficiencyErdal Eren, Tuba Edgünlü, Emre Asut, et al.Journal of Clinical Research in Pediatric Endocrinology|October 17, 2023
Clinical Variability in a Family with Noonan Syndrome with a Homozygous PTPN11 Gene Variant in Two IndividualsRuken Yıldırım, Edip Unal, Şervan Özalkak, et al.Pageof 112