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Page 1
Severe combined immunodeficiency resulting from mutations in MTHFD1.
Keller MD, Ganesh J, Heltzer M, Paessler M, Bergqvist AG, Baluarte HJ, Watkins D, Rosenblatt DS, Orange JS. Keller MD, et al. Among authors: heltzer m. Pediatrics. 2013 Feb;131(2):e629-34. doi: 10.1542/peds.2012-0899. Epub 2013 Jan 6. Pediatrics. 2013. PMID: 23296427
Immune dysregulation in severe influenza.
Heltzer ML, Coffin SE, Maurer K, Bagashev A, Zhang Z, Orange JS, Sullivan KE. Heltzer ML, et al. J Leukoc Biol. 2009 Jun;85(6):1036-43. doi: 10.1189/jlb.1108710. J Leukoc Biol. 2009. PMID: 19276177 Free PMC article.
Monosomy 1p36 uncovers a role for OX40 in survival of activated CD4+ T cells.
Suhoski MM, Perez EE, Heltzer ML, Laney A, Shaffer LG, Saitta S, Nachman S, Spinner NB, June CH, Orange JS. Suhoski MM, et al. Among authors: heltzer ml. Clin Immunol. 2008 Aug;128(2):181-9. doi: 10.1016/j.clim.2008.03.522. Epub 2008 Jun 3. Clin Immunol. 2008. PMID: 18511345 Free PMC article.
A potential screening tool for IPEX syndrome.
Heltzer ML, Choi JK, Ochs HD, Sullivan KE, Torgerson TR, Ernst LM. Heltzer ML, et al. Pediatr Dev Pathol. 2007 Mar-Apr;10(2):98-105. doi: 10.2350/06-07-0130.1. Pediatr Dev Pathol. 2007. PMID: 17378693