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Journal of Vascular Surgery|February 6, 2025
Outcomes for Hispanic patients undergoing open bypass in BEST-CLIJesus G Ulloa, Olamide Alabi, Katharine McGinigle, et al.
The Journal of Clinical Endocrinology and Metabolism|May 16, 2017
Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing DiseaseFabio R Faucz, Amit Tirosh, Christina Tatsi, et al.
JCI Insight|October 27, 2020
Requirement of FAT and DCHS protocadherins during hypothalamic-pituitary developmentEmily J Lodge, Paraskevi Xekouki, Tatiane S Silva, et al.
Endocrine-Related Cancer|May 24, 2017
Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's diseaseLaura C Hernández-Ramírez, Ryhem Gam, Nuria Valdés, et al.
American Journal of Medical Genetics. Part A|August 6, 2021
Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 childrenGeorgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
Frontiers in Endocrinology|July 28, 2020
Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?Idoia Martínez de LaPiscina, Laura C Hernández-Ramírez, Nancy Portillo, et al.
JAMA Network Open|September 9, 2024
Sustained Performance of Cardiac Arrest Prevention in Pediatric Cardiac Intensive Care UnitsDana Mueller, David K Bailly, Mousumi Banerjee, et al.
Birth Defects Research|March 11, 2022
Exome sequencing identifies variants in infants with sacral agenesisGeorgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
JAMA Pediatrics|July 5, 2022
Preventing Cardiac Arrest in the Pediatric Cardiac Intensive Care Unit Through Multicenter CollaborationJeffrey Alten, David S Cooper, Darren Klugman, et al.
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