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Hormone Research in Paediatrics|June 15, 2018
Congenital Hyperinsulinism in Infants with Turner Syndrome: Possible Association with Monosomy X and KDM6A HaploinsufficiencyChristopher E Gibson, Kara E Boodhansingh, Changhong Li, et al.
Human Molecular Genetics|June 9, 1998
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystoniaC Klein, M F Brin, D de Leon, et al.
Antioxidants & Redox Signaling|June 14, 2013
Mechanotransduction drives post ischemic revascularization through K(ATP) channel closure and production of reactive oxygen speciesElizabeth Browning, Hui Wang, Nankang Hong, et al.
The Journal of Clinical Endocrinology and Metabolism|August 18, 2021
Effect of Sitagliptin on Islet Function in Pancreatic Insufficient Cystic Fibrosis With Abnormal Glucose ToleranceAndrea Kelly, Saba Sheikh, Darko Stefanovski, et al.
Journal of Arrhythmia|September 17, 2025
Establishing a Cardiac Implantable Electronic Device Lead Extraction Program in a Resource-Limited SettingGiselle G Gervacio, Jhobeleen D De Leon, Michael Joseph C Agbayani, et al.
European Journal of Endocrinology|June 8, 2022
Localized islet nuclear enlargement hyperinsulinism (LINE-HI) due to ABCC8 and GCK mosaic mutationsKara E Boodhansingh, Zhongying Yang, Changhong Li, et al.
Genomics|January 25, 2000
The TOR1A (DYT1) gene family and its role in early onset torsion dystoniaL J Ozelius, C E Page, C Klein, et al.
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