Prader Willi Syndrome
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference149 articles.
1. Prader-Willi and Angelman syndromes: sister imprinted disorders;Cassidy;Am J Med Genet,2000
2. Mouse models of Prader–Willi syndrome: a systematic review;Bervini;Front Neuroendocrinol,2013
3. Necdin, a Prader–Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development;Miller;Hum Mol Genet,2009
4. Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome;Bischof;Hum Mol Genet,2007
5. SnoRNA Snord116 deletion causes growth deficiency and hyperphagia in mice;Ding;PLoS One,2008
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1. Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editing;2024-03-04
2. Syndromic and Monogenic Obesity: New Opportunities Due to Genetic-Based Pharmacological Treatment;Children;2024-01-25
3. Increased IGFBP Proteolysis, IGF-I Bioavailability, and Pappalysin Levels in Children With Prader-Willi Syndrome;The Journal of Clinical Endocrinology & Metabolism;2023-12-23
4. Management of Monogenic and Syndromic Obesity;Gastroenterology Clinics of North America;2023-12
5. Differences in spinal postures and mobility among adults with Prader-Willi syndrome, essential obesity, and normal-weight individuals;Frontiers in Endocrinology;2023-09-20
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