Hereditärer primärer Hyperparathyreoidismus
Author:
Publisher
Springer Berlin Heidelberg
Link
https://link.springer.com/content/pdf/10.1007/978-3-662-61724-3_25-2
Reference110 articles.
1. Abdullayev T et al (2020) A rare cause of neonatal hypercalcemia: neonatal severe primary hyperparathyroidism: a case report and review of the literature. Int J Surg Case Rep 66:365–369. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957862/?report=abstract. Zugegriffen am 07.08.2020
2. Agarwal SK, Mateo CM, Marx SJ (2009) Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states. J Clin Endocrinol Metab 94(5):1826–1834. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2684477/?report=abstract. Zugegriffen am 29.07.2020
3. Alevizaki M, Saltiki K (2015) Primary hyperparathyroidism in MEN2 syndromes. In: Recent results in cancer research. Springer, New York LLC, S 179–186
4. Allendorf J et al (2007) 1112 consecutive bilateral neck explorations for primary hyperparathyroidism. World J Surg 31(11):2075–2080. https://pubmed.ncbi.nlm.nih.gov/17768656/. Zugegriffen am 08.08.2020
5. Alrezk R, Hannah-Shmouni F, Stratakis CA (2017) MEN4 and CDKN1B mutations: The latest of the MEN syndromes. Endocr Relat Cancer 24(10):T195–T208
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