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X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options.
Albert MH, Bittner TC, Nonoyama S, Notarangelo LD, Burns S, Imai K, Espanol T, Fasth A, Pellier I, Strauss G, Morio T, Gathmann B, Noordzij JG, Fillat C, Hoenig M, Nathrath M, Meindl A, Pagel P, Wintergerst U, Fischer A, Thrasher AJ, Belohradsky BH, Ochs HD. Albert MH, et al. Among authors: noordzij jg. Blood. 2010 Apr 22;115(16):3231-8. doi: 10.1182/blood-2009-09-239087. Epub 2010 Feb 19. Blood. 2010. PMID: 20173115 Free article.
BTKbase, mutation database for X-linked agammaglobulinemia (XLA).
Vihinen M, Brandau O, Brandén LJ, Kwan SP, Lappalainen I, Lester T, Noordzij JG, Ochs HD, Ollila J, Pienaar SM, Riikonen P, Saha BK, Smith CI. Vihinen M, et al. Among authors: noordzij jg. Nucleic Acids Res. 1998 Jan 1;26(1):242-7. doi: 10.1093/nar/26.1.242. Nucleic Acids Res. 1998. PMID: 9399844 Free PMC article.
Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrow.
Noordzij JG, Verkaik NS, van der Burg M, van Veelen LR, de Bruin-Versteeg S, Wiegant W, Vossen JM, Weemaes CM, de Groot R, Zdzienicka MZ, van Gent DC, van Dongen JJ. Noordzij JG, et al. Blood. 2003 Feb 15;101(4):1446-52. doi: 10.1182/blood-2002-01-0187. Epub 2002 Oct 24. Blood. 2003. PMID: 12406895 Free article.
Reviewing Omenn syndrome.
Aleman K, Noordzij JG, de Groot R, van Dongen JJ, Hartwig NG. Aleman K, et al. Among authors: noordzij jg. Eur J Pediatr. 2001 Dec;160(12):718-25. doi: 10.1007/s004310100816. Eur J Pediatr. 2001. PMID: 11795679 Review.
36 results