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Familial hypocalciuric hypercalcaemia: a review.
Christensen SE, Nissen PH, Vestergaard P, Mosekilde L. Christensen SE, et al. Curr Opin Endocrinol Diabetes Obes. 2011 Dec;18(6):359-70. doi: 10.1097/MED.0b013e32834c3c7c. Curr Opin Endocrinol Diabetes Obes. 2011. PMID: 21986511 Review.
Molecular genetic analysis of the calcium sensing receptor gene in patients clinically suspected to have familial hypocalciuric hypercalcemia: phenotypic variation and mutation spectrum in a Danish population.
Nissen PH, Christensen SE, Heickendorff L, Brixen K, Mosekilde L. Nissen PH, et al. Among authors: christensen se. J Clin Endocrinol Metab. 2007 Nov;92(11):4373-9. doi: 10.1210/jc.2007-0322. Epub 2007 Aug 14. J Clin Endocrinol Metab. 2007. PMID: 17698911
Multiplex ligation-dependent probe amplification (MLPA) screening for exon copy number variation in the calcium sensing receptor gene: no large rearrangements identified in patients with calcium metabolic disorders.
Nissen PH, Christensen SE, Wallace A, Heickendorff L, Brixen K, Mosekilde L. Nissen PH, et al. Among authors: christensen se. Clin Endocrinol (Oxf). 2010 Jun;72(6):758-62. doi: 10.1111/j.1365-2265.2009.03750.x. Epub 2009 Nov 11. Clin Endocrinol (Oxf). 2010. PMID: 19912241
Vitamin D metabolites and skeletal consequences in primary hyperparathyroidism.
Moosgaard B, Christensen SE, Vestergaard P, Heickendorff L, Christiansen P, Mosekilde L. Moosgaard B, et al. Among authors: christensen se. Clin Endocrinol (Oxf). 2008 May;68(5):707-15. doi: 10.1111/j.1365-2265.2007.03109.x. Epub 2007 Nov 2. Clin Endocrinol (Oxf). 2008. PMID: 17980013
123 results