Showing results (11-20 of 125) with videos related to
Sort By:
Pageof 13
Pediatric Cardiology|June 17, 2010
Successful congenital heart surgery for a toddler with idiopathic infantile arterial calcificationMargaret M Samyn, David Bick, John A Humphrey, et al.The Journal of Pediatrics|March 1, 2020
The Evaluation of Hematologic Screening and Perioperative Management in Patients with Noonan Syndrome: A Retrospective Chart ReviewBenjamin Briggs, Dipal Savla, Nanda Ramchandar, et al.The Journal of Pediatrics|January 16, 2023
Novel Approach to Improve the Identification of the Bleeding Phenotype in Noonan Syndrome and Related RASopathiesLeah Bruno, Jerica Lenberg, Dzung Le, et al.Human Gene Therapy|October 27, 2010
Correction of hyperbilirubinemia in gunn rats using clinically relevant low doses of helper-dependent adenoviral vectorsDavid Dimmock, Nicola Brunetti-Pierri, Donna J Palmer, et al.Journal of Medical Genetics|April 27, 2019
Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseasesDavid Bick, Marilyn Jones, Stacie L Taylor, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|June 30, 2015
EFTUD2 deficiency in vertebrates: Identification of a novel human mutation and generation of a zebrafish modelBrett Deml, Linda M Reis, Sanaa Muheisen, et al.BMC Neurology|November 24, 2017
The humanistic burden of Pompe disease: are there still unmet needs? A systematic reviewBenedikt Schoser, Deborah A Bilder, David Dimmock, et al.Neuromuscular Disorders : NMD|September 9, 2009
Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutationsJames Collins, Kevin E Bove, David Dimmock, et al.The Journal of Pediatrics|May 23, 2021
Implementing Rapid Whole-Genome Sequencing in Critical Care: A Qualitative Study of Facilitators and Barriers to New Technology AdoptionLinda S Franck, Rebecca M Kriz, Seema Rego, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 26, 2021
Reducing Sanger confirmation testing through false positive prediction algorithmsJames M Holt, Melissa Kelly, Brett Sundlof, et al.Pageof 13