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Page 1
Severe Pediatric COVID-19 and Multisystem Inflammatory Syndrome in Children From Wild-type to Population Immunity: A Prospective Multicenter Cohort Study With Real-time Reporting.
Pediatr Infect Dis J. 2023 Dec 1;42(12):1077-1085. doi: 10.1097/INF.0000000000004098. Epub 2023 Oct 12.
Pediatr Infect Dis J. 2023.
PMID: 37823702
Free PMC article.
Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy.
Weterman MA, Barth PG, van Spaendonck-Zwarts KY, Aronica E, Poll-The BT, Brouwer OF, van Tintelen JP, Qahar Z, Bradley EJ, de Wissel M, Salviati L, Angelini C, van den Heuvel L, Thomasse YE, Backx AP, Nürnberg G, Nürnberg P, Baas F.
Weterman MA, et al.
Brain. 2013 Jan;136(Pt 1):282-93. doi: 10.1093/brain/aws293.
Brain. 2013.
PMID: 23365102
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Comment on: prenatal exposure to acid-suppressive drugs and the risk of allergic disease in the offspring: a cohort study.
Petrus NC, Thomasse YE, Sprikkelman AB, van Aalderen WM, ten Tusscher GW.
Petrus NC, et al.
Clin Exp Allergy. 2014 Jul;44(7):1003-4. doi: 10.1111/cea.12336.
Clin Exp Allergy. 2014.
PMID: 24953634
No abstract available.
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An 8.35 Mb overlapping interstitial deletion of 8q24 in two patients with coloboma, congenital heart defect, limb abnormalities, psychomotor retardation and convulsions.
Verheij JB, de Munnik SA, Dijkhuizen T, de Leeuw N, Olde Weghuis D, van den Hoek GJ, Rijlaarsdam RS, Thomasse YE, Dikkers FG, Marcelis CL, van Ravenswaaij-Arts CM.
Verheij JB, et al.
Eur J Med Genet. 2009 Sep-Oct;52(5):353-7. doi: 10.1016/j.ejmg.2009.05.006. Epub 2009 May 21.
Eur J Med Genet. 2009.
PMID: 19464398
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