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| A rare association of central hypothyroidism and adrenal insufficiency in a boy with Williams-Beuren syndrome | |
| Devi Dayal, Dinesh Giri, Senthil Senniappan | |
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Ann Pediatr Endocrinol Metab. 2017;22(1):65-67. Published online March 31, 2017 DOI: https://doi.org/10.6065/apem.2017.22.1.65 |
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A rare association of central hypothyroidism and adrenal insufficiency in a boy with Williams-Beuren syndrome Annals of Pediatric Endocrinology & Metabolism. 2017;22(1):65  Ibrutinib Reactions Weekly. 2021;1851(1):179-179 CORRIGENDUM for “Central Adrenal Insufficiency Is Rare in Adults With Prader–Willi Syndrome” The Journal of Clinical Endocrinology & Metabolism. 2020;105(8):e3052-e3052 Nivolumab Reactions Weekly. 2019;1770(1):306-306 Diagnostik und Therapie beim Williams-Beuren-Syndrom (WBS) Monatsschrift Kinderheilkunde. 2005;153(3):273-280 Williams Syndrome (Williams-Beuren syndrome, WMS) Encyclopedia of Genetics, Genomics, Proteomics and Informatics. 2008;2103-2104 Williams-Beuren Syndrome With Primary Hyperparathyroidism: A Rare Diagnosis In A Rare Genetic Syndrome AACE Clinical Case Reports. 2017;3(3):e213-e216 Williams–Beuren Syndrome Encyclopedia of Clinical Neuropsychology. 2011;2718-2718 A case of Dyke-Davidoff-Masson syndrome associated with central hypothyroidism and secondary adrenal insufficiency Hormones. 2013;12(3):461-465 Williams-Beuren Syndrome Encyclopedia of Child Behavior and Development. 2011;1571-1571 |
