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Journal of Clinical Research in Pediatric Endocrinology|February 10, 2021
Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary HypocalcemiaElvan Bayramoğlu, Melikşah Keskin, Zehra Aycan, et al.
Journal of Clinical Research in Pediatric Endocrinology|February 10, 2021
Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi SyndromeAydilek Dağdeviren Çakır, Firdevs Baş, Onur Akın, et al.
Journal of Clinical Research in Pediatric Endocrinology|September 26, 2019
Association of Total and High Molecular Weight Adiponectin with Components of Metabolic Syndrome in Mexican ChildrenJavier A. Magaña Gomez, Daniela Moreno-Mascareño, Carla E. Angulo Rojo, et al.
Journal of Clinical Research in Pediatric Endocrinology|September 14, 2019
Soluble Receptor for Glycation End-products Concentration Increases Following the Treatment of Severe Diabetic KetoacidosisWilliam H. Hoffman, Takaki Ishikawa, James Blum, et al.
Journal of Clinical Research in Pediatric Endocrinology|November 7, 2018
Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National SurveyErdal Eren, Ayça Törel Ergür, Şükriye Pınar İşgüven, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 13, 2019
Antimüllerian Hormone Levels of Infants with Premature ThelarcheNursel Muratoğlu Şahin, Elvan Bayramoğlu, Hatice Nursun Özcan, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 20, 2021
Genetic Indices Relationship to Hyperglycemia-associated Biomarkers: Consistency with miRNA Expression in Egyptian Children with T1DMNaglaa Fathy Barseem, Marwa Mohamed Mahasab, Ibrahem Fathy Zaed, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 26, 2019
Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel KISS1R/GPR54 Loss-of-Function MutationÖzlem Nalbantoğlu, Gülçin Arslan, Özge Köprülü, et al.
Journal of Clinical Research in Pediatric Endocrinology|July 7, 2012
Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadismFatih Gürbüz, L Damla Kotan, Eda Mengen, et al.
Journal of Clinical Research in Pediatric Endocrinology|September 19, 2012
Is premature thelarche in the first two years of life transient?Ahmet Uçar, Nurçin Saka, Firdevs Baş, et al.
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