Showing results (31-40 of 77) with videos related to

Sort By:
Pageof 8
Ophthalmic Genetics|July 26, 2023
Cryptophthalmos: associated syndromes and genetic disordersDaphna Landau-Prat, Diana H Kim, Sana Bautista, et al.
Journal of Inherited Metabolic Disease|December 10, 2024
Executive and adaptive function impacts long-term outcomes for adults with maple syrup urine diseaseJessica I Gold, Alanna Strong, Nina B Gold, et al.
American Journal of Medical Genetics. Part A|May 25, 2023
TOPORS as a novel causal gene for Joubert syndromeAlanna Strong, Hui-Qi Qu, Sinéad Cullina, et al.
Circulation Research|January 17, 2015
Macrophage sortilin promotes LDL uptake, foam cell formation, and atherosclerosisKevin M Patel, Alanna Strong, Junichiro Tohyama, et al.
European Journal of Pediatrics|July 1, 2023
The real world experience of pediatric primary hyperoxaluria patients in the PEDSnet clinical research networkChristina B Ching, Kimberley Dickinson, John Karafilidis, et al.
American Journal of Medical Genetics. Part A|June 16, 2021
Expanding the genetic landscape of oral-facial-digital syndrome with two novel genesAlanna Strong, Laurie Simone, Anthony Krentz, et al.
Journal of Pediatric Urology|October 17, 2023
Distinguishing characteristics of pediatric patients with primary hyperoxaluria type 1 in PEDSnetGregory E Tasian, Kimberley Dickinson, Grace Park, et al.
The Journal of Pediatric Pharmacology and Therapeutics : JPPT : the Official Journal of PPAG|March 22, 2016
Pharmacokinetics of Continuous Infusion Meropenem With Concurrent Extracorporeal Life Support and Continuous Renal Replacement Therapy: A Case ReportJeffrey J Cies, Wayne S Moore, Susan B Conley, et al.
Pageof 8