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The Journal of Pediatrics|November 16, 2010
Association between oxidative stress and masked hypertension in a multi-ethnic population of obese children and adolescentsVlady Ostrow, Shufang Wu, Alexandra Aguilar, et al.Data in Brief|June 29, 2023
Geoprocess of geospatial urban data in Tallinn, EstoniaNasim Eslamirad, Francesco De Luca, Kimmo Sakari Lylykangas, et al.Case Reports in Obstetrics and Gynecology|June 15, 2017
Epidural Anesthesia for Cesarean Section in a Pregnant Woman with Marfan Syndrome and Dural EctasiaFranco Pepe, Mariagrazia Stracquadanio, Francesco De Luca, et al.Urologia|October 25, 2011
[Laparoscopic repair of rectovesical fistula after radical retropubic prostatectomy]Paolo Parma, Alessandro Samuelli, Bruno Dall'Oglio, et al.Physical Review. E|March 18, 2023
Finite-size criticality in fully connected spin models on superconducting quantum hardwareMichele Grossi, Oriel Kiss, Francesco De Luca, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|May 29, 2024
Computed tomography-guided percutaneous cryoablation of hereditary adrenal pheochromocytoma in three patientsEmily Griffing, Brenton Reading, Francesco De Luca, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 5, 2003
Effects of Ca2+ sensing receptor activation in the growth plateShufang Wu, Teresa Palese, Om Prakash Mishra, et al.The Journal of Biological Chemistry|August 14, 2013
Increased expression of fibroblast growth factor 21 (FGF21) during chronic undernutrition causes growth hormone insensitivity in chondrocytes by inducing leptin receptor overlapping transcript (LEPROT) and leptin receptor overlapping transcript-like 1 (LEPROTL1) expressionShufang Wu, Tal Grunwald, Alexei Kharitonenkov, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|December 16, 2016
Vitamin D supplementation, the metabolic syndrome and oxidative stress in obese childrenTal Grunwald, Shruti Fadia, Bruce Bernstein, et al.Journal of Cardiovascular Electrophysiology|October 3, 2025
A Novel Variant in SLC4A3 Gene Mutation Associated With Familial Short QT Syndrome and Sudden DeathPasquale Crea, Carla Giustetto, Antonino Micari, et al.Pageof 10