Similar articles

• Chondrocalcinosis related to familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

  Cimbek EA, Şen Y, Yuca SA, Peru H. Cimbek EA, et al. J Pediatr Endocrinol Metab. 2015 May;28(5-6):713-6. doi: 10.1515/jpem-2013-0254. J Pediatr Endocrinol Metab. 2015. PMID: 25720051
• Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene.

  Conticini E, Negro A, Magnani L, Ugolini R, Atienza-Mateo B, Frediani B, Salvarani C. Conticini E, et al. Reumatismo. 2020 Apr 10;72(1):67-70. doi: 10.4081/reumatismo.2020.1255. Reumatismo. 2020. PMID: 32292023
• Rather Unusual Cause of Seizures.

  Singh P, Miao J, Schwartz GL. Singh P, et al. Am J Med. 2021 Jun;134(6):e380-e381. doi: 10.1016/j.amjmed.2020.11.015. Epub 2021 Jan 14. Am J Med. 2021. PMID: 33359777 No abstract available.
• Mechanisms and causes of hypomagnesemia.

  Agus ZS. Agus ZS. Curr Opin Nephrol Hypertens. 2016 Jul;25(4):301-7. doi: 10.1097/MNH.0000000000000238. Curr Opin Nephrol Hypertens. 2016. PMID: 27219040 Review.
• Genetic causes of hypomagnesemia, a clinical overview.

  Viering DHHM, de Baaij JHF, Walsh SB, Kleta R, Bockenhauer D. Viering DHHM, et al. Pediatr Nephrol. 2017 Jul;32(7):1123-1135. doi: 10.1007/s00467-016-3416-3. Epub 2016 May 27. Pediatr Nephrol. 2017. PMID: 27234911 Free PMC article. Review.