Multicentric Italian case–control study on 25OH vitamin D levels in children and adolescents with Prader-Willi syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s40618-022-01990-5.pdf
Reference55 articles.
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2. Butler MG, Hartin SN, Hossain WA et al (2019) Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study. J Med Genet 56(3):149–153
3. Cassidy SB, Schwartz S, Miller JL, Driscoll DJ (2012) Prader-Willi syndrome. Genet Med 14:10–26
4. Angulo MA, Butler MG, Cataletto ME (2015) Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings. J Endocrinol Invest 38(12):1249–1263
5. Bochukova EG, Lawler K, Croizier S, Keogh JM, Patel N, Strohbehn G, Lo KK, Humphrey J, Hokken-Koelega A, Damen L, Donze S, Bouret SG, Plagnol V, Farooqi IS (2018) A transcriptomic signature of the hypothalamic response to fasting and BDNF deficiency in Prader-Willi Syndrome. Cell Rep 22:3401–3408
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1. Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation;Frontiers in Endocrinology;2024-04-26
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