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Current Opinion in Pediatrics|August 22, 2022
Advancements in therapeutics for inborn errors of metabolismAlicia Turner, Kevin E Glinton, V Reid SuttonPediatric Clinics of North America|March 6, 2018
Newborn Screening: History, Current Status, and Future DirectionsAyman W El-Hattab, Mohammed Almannai, V Reid SuttonAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 9, 2016
Phenotypic and molecular characterization of focal dermal hypoplasia in 18 individualsBret Bostwick, Ping Fang, Ankita Patel, et al.Case Reports in Obstetrics and Gynecology|August 1, 2022
Obstetrical Challenges in Robinow SyndromeYingao Zhang, Marco Casanova, Matthew Shanahan, et al.Journal of Child Neurology|October 18, 2005
Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapyRuthie E Amir, V Reid Sutton, Ignatia B Van den VeyverMolecular Genetics and Metabolism|February 1, 2003
A mouse model of argininosuccinic aciduria: biochemical characterizationV Reid Sutton, Yanzhen Pan, Erica C Davis, et al.Rheumatology (Oxford, England)|February 9, 2021
Clinical significance of E148Q heterozygous variant in paediatric familial Mediterranean feverIrit Tirosh, Yonatan Yacobi, Asaf Vivante, et al.Molecular Genetics and Metabolism|September 11, 2017
Quantitation of phenylbutyrate metabolites by UPLC-MS/MS demonstrates inverse correlation of phenylacetate:phenylacetylglutamine ratio with plasma glutamine levelsYi Jiang, Mohammed Almannai, V Reid Sutton, et al.Journal of Human Genetics|March 18, 2016
Nineteen-year follow-up of a patient with severe glutathione synthetase deficiencyPaldeep S Atwal, Casey R Medina, Lindsay C Burrage, et al.Clinical Dysmorphology|June 7, 2007
Parkes Weber syndrome occurring in a family with capillary malformationsNicola Brunetti-Pierri, Glen F Seidel, Moise L Levy, et al.Pageof 18