Human neonatal hypocalcemia.
Salle BL, Delvin E, Glorieux F, David L.
Biol Neonate. 1990;58 Suppl 1:22-31. doi: 10.1159/000243297.
Channelopathies.
Kim JB.
Korean J Pediatr. 2014 Jan;57(1):1-18. doi: 10.3345/kjp.2014.57.1.1. Epub 2014 Jan 31.
Bartter Syndrome.
Bokhari SRA, Zulfiqar H, Mansur A.
2023 Sep 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–.
Neonatal transitory hypomagnesaemia.
Lukács VF.
Acta Paediatr Acad Sci Hung. 1972;13(4):341-4.
Transient neonatal hypocalcaemia caused by maternal hyperparathyroidism.
Gonçalves JS, Queiró LC, Soares J, Correia CR.
BMJ Case Rep. 2022 Mar 16;15(3):e248262. doi: 10.1136/bcr-2021-248262.
[Pharmacovigilance].
Livio F, Renard D, Buclin T.
Rev Med Suisse. 2012 Jan 18;8(324):116-9.
Primary infantile hypomagnesaemia.
Smales OR.
Proc R Soc Med. 1974 Aug;67(8):759-60. doi: 10.1177/003591577406700836.
Hypomagnesaemia is absent in children with autosomal dominant polycystic kidney disease.
Seeman T, Fořtová M, Sopko B, Průša R, Pohl M, John U.
Ann Clin Biochem. 2019 Jan;56(1):90-94. doi: 10.1177/0004563218785190. Epub 2018 Jul 2.
[Hypocalcemia].
Garabédian M.
Rev Prat. 1998 Jun 1;48(11):1201-6.
Refeeding Syndrome in the Neonatal Intensive Care Unit.
Bradford CV, Cober MP, Miller JL.
J Pediatr Pharmacol Ther. 2021;26(8):771-782. doi: 10.5863/1551-6776-26.8.771. Epub 2021 Nov 10.
