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Pediatrics|March 16, 2011
Growth standards of infants with Prader-Willi syndromeMerlin G Butler, Jennifer Sturich, Jaehoon Lee, et al.Clinical Pediatrics|February 5, 2016
Growth Charts for Prader-Willi Syndrome During Growth Hormone TreatmentMerlin G Butler, Jaehoon Lee, Devin M Cox, et al.Genes|November 9, 2019
Early Diagnosis in Prader-Willi Syndrome Reduces Obesity and Associated Co-MorbiditiesVirginia E Kimonis, Roy Tamura, June-Anne Gold, et al.Journal of Clinical Medicine|May 14, 2022
Molecular Classes and Growth Hormone Treatment Effects on Behavior and Emotion in Patients with Prader-Willi SyndromeRanim Mahmoud, Heidi D Swanson, Merlin G Butler, et al.American Journal of Medical Genetics. Part A|April 6, 2011
Nutritional phases in Prader-Willi syndromeJennifer L Miller, Christy H Lynn, Danielle C Driscoll, et al.Neuroscience Letters|July 1, 2009
Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndromeHailing Su, Weiwei Fan, Pinar E Coskun, et al.Journal of Medical Genetics|May 7, 2018
Molecular genetic classification in Prader-Willi syndrome: a multisite cohort studyMerlin G Butler, Samantha N Hartin, Waheeda A Hossain, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 10, 2013
Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technologyJune-Anne Gold, Chelsey Ruth, Kathryn Osann, et al.Pediatric Neurology|August 13, 2021
Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental SyndromesOlivia J Veatch, Beth A Malow, Hye-Seung Lee, et al.Genome Medicine|March 27, 2019
Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndromeFrancesco Vetrini, Shane McKee, Jill A Rosenfeld, et al.Pageof 4