Behavioral Phenotype of Patients with Prader-Willi Syndrome
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-67929-3_77-1
Reference49 articles.
1. Bar C, Diene G, Molinas C et al (2017) Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome. Orphanet J Rare Dis 12:118. https://doi.org/10.1186/s13023-017-0673-6
2. Bellis SA, Kuhn I, Adams S et al (2022) The consequences of hyperphagia in people with Prader-Willi syndrome: a systematic review of studies of morbidity and mortality. Eur J Med Genet 65:104379. https://doi.org/10.1016/j.ejmg.2021.104379
3. Bigi N, Faure J-M, Coubes C et al (2008) Prader-Willi syndrome: is there a recognizable fetal phenotype? Prenat Diagn 28:796–799. https://doi.org/10.1002/pd.1973
4. Boer H, Holland A, Whittington J et al (2002) Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy. Lancet 359:135–136. https://doi.org/10.1016/S0140-6736(02)07340-3
5. Bonnot O, Cohen D, Thuilleaux D et al (2016) Psychotropic treatments in Prader-Willi syndrome: a critical review of published literature. Eur J Pediatr 175:9–18. https://doi.org/10.1007/s00431-015-2670-x
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