Noordzij JG - Search Results

1

The 78C --> T (T254M) XHIM mutation: lack of a tight phenotype-genotype relationship.

de Vries E, Noordzij JG, Davies EG, Hartwig N, Breuning MH, van Dongen JJ, van Tol MJ. de Vries E, et al. Among authors: noordzij jg. Blood. 1999 Aug 15;94(4):1488-90. Blood. 1999. PMID: 10484640 Free article. No abstract available.

2

N-terminal truncated human RAG1 proteins can direct T-cell receptor but not immunoglobulin gene rearrangements.

Noordzij JG, Verkaik NS, Hartwig NG, de Groot R, van Gent DC, van Dongen JJ. Noordzij JG, et al. Blood. 2000 Jul 1;96(1):203-9. Blood. 2000. PMID: 10891452 Free article.

3

[Widely divergent clinical phenotype of x-linked agammaglobulinemia in two cousins].

Jansen AG, Noordzij JG, Bröcker-Vriends AH, van Dongen JJ, van Tol MJ, Bredius RG. Jansen AG, et al. Among authors: noordzij jg. Ned Tijdschr Geneeskd. 2004 May 22;148(21):1053-6. Ned Tijdschr Geneeskd. 2004. PMID: 15185441 Dutch.

4

The immunophenotypic and immunogenotypic B-cell differentiation arrest in bone marrow of RAG-deficient SCID patients corresponds to residual recombination activities of mutated RAG proteins.

Noordzij JG, de Bruin-Versteeg S, Verkaik NS, Vossen JM, de Groot R, Bernatowska E, Langerak AW, van Gent DC, van Dongen JJ. Noordzij JG, et al. Blood. 2002 Sep 15;100(6):2145-52. Blood. 2002. PMID: 12200379 Free article.

5

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.

6

Composition of precursor B-cell compartment in bone marrow from patients with X-linked agammaglobulinemia compared with healthy children.

Noordzij JG, de Bruin-Versteeg S, Comans-Bitter WM, Hartwig NG, Hendriks RW, de Groot R, van Dongen JJ. Noordzij JG, et al. Pediatr Res. 2002 Feb;51(2):159-68. doi: 10.1203/00006450-200202000-00007. Pediatr Res. 2002. PMID: 11809909

7

Flow cytometric immunophenotyping in the diagnosis and follow-up of immunodeficient children.

de Vries E, Noordzij JG, Kuijpers TW, van Dongen JJ. de Vries E, et al. Among authors: noordzij jg. Eur J Pediatr. 2001 Oct;160(10):583-91. doi: 10.1007/s004310100797. Eur J Pediatr. 2001. PMID: 11686500 Review.

8

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.

9

Two patients with complete defects in interferon gamma receptor-dependent signaling.

Noordzij JG, Hartwig NG, Verreck FA, De Bruin-Versteeg S, De Boer T, Van Dissel JT, De Groot R, Ottenhoff TH, Van Dongen JJ. Noordzij JG, et al. J Clin Immunol. 2007 Sep;27(5):490-6. doi: 10.1007/s10875-007-9097-8. Epub 2007 May 21. J Clin Immunol. 2007. PMID: 17514500 Free article.

10

XLA patients with BTK splice-site mutations produce low levels of wild-type BTK transcripts.

Noordzij JG, de Bruin-Versteeg S, Hartwig NG, Weemaes CM, Gerritsen EJ, Bernatowska E, van Lierde S, de Groot R, van Dongen JJ. Noordzij JG, et al. J Clin Immunol. 2002 Sep;22(5):306-18. doi: 10.1023/a:1019982206951. J Clin Immunol. 2002. PMID: 12405164

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