{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,2,10]],"date-time":"2024-02-10T00:15:45Z","timestamp":1707524145530},"reference-count":14,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2020,9,23]]},"DOI":"10.7759\/cureus.10625","type":"journal-article","created":{"date-parts":[[2020,9,24]],"date-time":"2020-09-24T05:40:03Z","timestamp":1600926003000},"source":"Crossref","is-referenced-by-count":0,"title":["Hypocalcemia and a Positive Metabolic Screen for Severe Combined Immunodeficiency in an 11-Day-Old Male With DiGeorge Syndrome"],"prefix":"10.7759","author":[{"given":"Jessica","family":"Ford","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jose M","family":"Pena","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shane C","family":"Rainey","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1038\/nrdp.2015.71","article-title":"22q11 deletion syndrome","volume":"1","author":"McDonald-McGinn DM","year":"2015","unstructured":"McDonald-McGinn DM, Sullivan KE, Marino B, et al.. 22q11 deletion syndrome. Nat Rev Dis Primers. 2015, 1:15071. 10.1038\/nrdp.2015.71","journal-title":"Nat Rev Dis Primers"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.30.10.852","article-title":"DiGeorge syndrome: part of CATCH 22","volume":"30","author":"Wilson DI","year":"1993","unstructured":"Wilson DI, Burn J, Scambler P, Goodship J. DiGeorge syndrome: part of CATCH 22.  J Med Genet. 1993, 30:852-856. 10.1136\/jmg.30.10.852","journal-title":"J Med Genet"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1007\/s00431-013-2240-z","article-title":"Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times","volume":"173","author":"Habel A","year":"2014","unstructured":"Habel A, Herriot R, Kumararatne D, et al.. Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times. Eur J Pediatr. 2014, 173:757-765. 10.1007\/s00431-013-2240-z","journal-title":"Eur J Pediatr"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1542\/peds.2011-2659","article-title":"Transient neonatal hypocalcemia: presentation and outcomes","volume":"129","author":"Thomas TC","year":"2012","unstructured":"Thomas TC, Smith JM, White PC, Adhikari S. Transient neonatal hypocalcemia: presentation and outcomes. Pediatrics. 2012, 129:1461-1467. 10.1542\/peds.2011-2659","journal-title":"Pediatrics"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1016\/j.siny.2003.10.002","article-title":"Perinatal calcium metabolism: physiology and pathophysiology","volume":"9","author":"Hsu SC","year":"2004","unstructured":"Hsu SC, Levine MA. Perinatal calcium metabolism: physiology and pathophysiology. Semin Neonatol. 2004, 9:23-36. 10.1016\/j.siny.2003.10.002","journal-title":"Semin Neonatol"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.3928\/0090-4481-19960401-09","article-title":"Common clinical manifestations of maternal diabetes in newborn infants: implications for the practicing pediatrician","volume":"25","author":"Rosenn B","year":"1996","unstructured":"Rosenn B, Miodovnik M, Tsang R. Common clinical manifestations of maternal diabetes in newborn infants: implications for the practicing pediatrician. Pediatr Ann. 1996, 25:215-222. 10.3928\/0090-4481-19960401-09","journal-title":"Pediatr Ann"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1111\/cen.12466","article-title":"Prevalence of hypocalcemia and its associated features in 22q11.2 deletion","volume":"81","author":"Cheung ENM","year":"2014","unstructured":"Cheung ENM, George SR, Costain GA, Andrade DM, Chow EWC, Silversides CK, Bassett AS. Prevalence of hypocalcemia and its associated features in 22q11.2 deletion. Clin Endocrinol (Oxf). 2014, 81:190-196. 10.1111\/cen.12466","journal-title":"Clin Endocrinol (Oxf)"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1001\/archpedi.1991.02160080119033","article-title":"Low serum calcium and high parathyroid hormone levels in neonates fed \u2018humanized\u2019 cow\u2019s milk-based formula","volume":"145","author":"Specker BL","year":"1991","unstructured":"Specker BL, Tsang RC, Ho ML, Landi TM, Gratton TL. Low serum calcium and high parathyroid hormone levels in neonates fed \u2018humanized\u2019 cow\u2019s milk-based formula. Am J Dis Child. 1991, 145:941-945. 10.1001\/archpedi.1991.02160080119033","journal-title":"Am J Dis Child"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1080\/14767058.2017.1331430","article-title":"Vitamin D levels in newborns and association with neonatal hypocalcemia","volume":"31","author":"Yilmaz B","year":"2018","unstructured":"Yilmaz B, Aygun C, Cetinoglu E. Vitamin D levels in newborns and association with neonatal hypocalcemia. J Matern Fetal Neonatal Med. 2018, 31:1889-1893. 10.1080\/14767058.2017.1331430","journal-title":"J Matern Fetal Neonatal Med"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(07)61601-8","article-title":"Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes","volume":"370","author":"Kobrynski LJ","year":"2007","unstructured":"Kobrynski LJ, Sullivan KE. Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes. Lancet. 2007, 370:1443-1452. 10.1016\/S0140-6736(07)61601-8","journal-title":"Lancet"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1007\/s10875-017-0403-9","article-title":"Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency","volume":"37","author":"Barry JC","year":"2017","unstructured":"Barry JC, Crowley TB, Jyonouchi S, Heimall J, Zachai EH, Sullivan KE, McDonald-McGinn DM. Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. J Clin Immunol. 2017, 37:476-485. 10.1007\/s10875-017-0403-9","journal-title":"J Clin Immunol"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1016\/j.jaci.2013.04.024","article-title":"Newborn screening for SCID and T cell lymphopenia in California: results of the first two years","volume":"132","author":"Kwan A","year":"2013","unstructured":"Kwan A, Church JA, Cowan MK, et al.. Newborn screening for SCID and T cell lymphopenia in California: results of the first two years. J Allergy Clin Immunol. 2013, 132:140-50. 10.1016\/j.jaci.2013.04.024","journal-title":"J Allergy Clin Immunol"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.1001\/jama.2009.1806","article-title":"Statewide newborn screening for severe T-cell lymphopenia","volume":"302","author":"Routes JM","year":"2009","unstructured":"Routes JM, Grossman WJ, Verbsky J, Laessig RH, Hoffman GL, Brokopp CD, Baker MW. Statewide newborn screening for severe T-cell lymphopenia. JAMA. 2009, 302:2465-2470. 10.1001\/jama.2009.1806","journal-title":"JAMA"},{"key":"ref14","doi-asserted-by":"publisher","DOI":"10.1007\/s10875-014-0006-7","article-title":"Newborn screening for SCID in New York state: experience from the first two years","volume":"34","author":"Vogel BH","year":"2015","unstructured":"Vogel BH, Bonagura V, Weinberg GA, et al.. Newborn screening for SCID in New York state: experience from the first two years. J Clin Immunol. 2015, 34:289-303. 10.1007\/s10875-014-0006-7","journal-title":"J Clin Immunol"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/20082-hypocalcemia-and-a-positive-metabolic-screen-for-severe-combined-immunodeficiency-in-an-11-day-old-male-with-digeorge-syndrome","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T19:23:22Z","timestamp":1707506602000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/20082-hypocalcemia-and-a-positive-metabolic-screen-for-severe-combined-immunodeficiency-in-an-11-day-old-male-with-digeorge-syndrome"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,9,23]]},"references-count":14,"URL":"https:\/\/doi.org\/10.7759\/cureus.10625","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2020,9,23]]}}}