Prader‐Willi Syndrome
- 17 March 2010
- book chapter
- other
- Published by Wiley
Abstract
No abstract availableThis publication has 128 references indexed in Scilit:
- Prader–Willi syndromeEuropean Journal of Human Genetics, 2008
- Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA clusterNature Genetics, 2008
- Gastric Rupture and Necrosis in Prader‐Willi SyndromeJournal of Pediatric Gastroenterology and Nutrition, 2007
- Deaths due to choking in Prader–Willi syndromeAmerican Journal of Medical Genetics Part A, 2006
- Growth hormone improves mobility and body composition in infants and toddlers with Prader-Willi syndromeThe Journal of Pediatrics, 2004
- Prader–Willi syndrome: Causes of death in an international series of 27 casesAmerican Journal of Medical Genetics Part A, 2003
- Pulmonary function abnormalities in Prader-Willi syndromeThe Journal of Pediatrics, 1995
- Weight management of youth with Prader-Willi syndromeInternational Journal of Eating Disorders, 1987
- Deletions of Chromosome 15 as a Cause of the Prader–Willi SyndromeThe New England Journal of Medicine, 1981
- Metabolic Aspects of a Protein-Sparing Modified Fast in the Dietary Management of Prader-Willi ObesityThe New England Journal of Medicine, 1977