Borte S - Search Results

1

Newborn screening for severe T and B cell lymphopenia identifies a fraction of patients with Wiskott-Aldrich syndrome.

Borte S, Fasth A, von Döbeln U, Winiarski J, Hammarström L. Borte S, et al. Clin Immunol. 2014 Nov;155(1):74-78. doi: 10.1016/j.clim.2014.09.003. Epub 2014 Sep 15. Clin Immunol. 2014. PMID: 25217881

2

Interleukin-21 restores immunoglobulin production ex vivo in patients with common variable immunodeficiency and selective IgA deficiency.

Borte S, Pan-Hammarström Q, Liu C, Sack U, Borte M, Wagner U, Graf D, Hammarström L. Borte S, et al. Among authors: borte m. Blood. 2009 Nov 5;114(19):4089-98. doi: 10.1182/blood-2009-02-207423. Epub 2009 Sep 8. Blood. 2009. PMID: 19738033 Free article.

3

Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR.

Borte S, von Döbeln U, Fasth A, Wang N, Janzi M, Winiarski J, Sack U, Pan-Hammarström Q, Borte M, Hammarström L. Borte S, et al. Among authors: borte m. Blood. 2012 Mar 15;119(11):2552-5. doi: 10.1182/blood-2011-08-371021. Epub 2011 Nov 30. Blood. 2012. PMID: 22130802 Free article.

4

Newborn screening for primary immunodeficiencies: beyond SCID and XLA.

Borte S, Wang N, Oskarsdóttir S, von Döbeln U, Hammarström L. Borte S, et al. Ann N Y Acad Sci. 2011 Dec;1246:118-30. doi: 10.1111/j.1749-6632.2011.06350.x. Ann N Y Acad Sci. 2011. PMID: 22236436

5

Placental transfer of maternally-derived IgA precludes the use of guthrie card eluates as a screening tool for primary immunodeficiency diseases.

Borte S, Janzi M, Pan-Hammarström Q, von Döbeln U, Nordvall L, Winiarski J, Fasth A, Hammarström L. Borte S, et al. PLoS One. 2012;7(8):e43419. doi: 10.1371/journal.pone.0043419. Epub 2012 Aug 16. PLoS One. 2012. PMID: 22916257 Free PMC article.

6

Guidelines for newborn screening of primary immunodeficiency diseases.

Borte S, von Döbeln U, Hammarström L. Borte S, et al. Curr Opin Hematol. 2013 Jan;20(1):48-54. doi: 10.1097/MOH.0b013e32835a9130. Curr Opin Hematol. 2013. PMID: 23108220 Review.

7

Impact of Down syndrome on the performance of neonatal screening assays for severe primary immunodeficiency diseases.

Verstegen RH, Borte S, Bok LA, van Zwieten PH, von Döbeln U, Hammarström L, de Vries E. Verstegen RH, et al. Among authors: borte s. J Allergy Clin Immunol. 2014 Apr;133(4):1208-11. doi: 10.1016/j.jaci.2013.10.010. Epub 2013 Dec 9. J Allergy Clin Immunol. 2014. PMID: 24332217 No abstract available.

8

Retrospective analysis of TREC based newborn screening results and clinical phenotypes in infants with the 22q11 deletion syndrome.

Lingman Framme J, Borte S, von Döbeln U, Hammarström L, Oskarsdóttir S. Lingman Framme J, et al. Among authors: borte s. J Clin Immunol. 2014 May;34(4):514-9. doi: 10.1007/s10875-014-0002-y. Epub 2014 Mar 9. J Clin Immunol. 2014. PMID: 24610337

9

The case for mandatory newborn screening for severe combined immunodeficiency (SCID).

Gaspar HB, Hammarström L, Mahlaoui N, Borte M, Borte S. Gaspar HB, et al. Among authors: borte s, borte m. J Clin Immunol. 2014 May;34(4):393-7. doi: 10.1007/s10875-014-0029-0. Epub 2014 Apr 2. J Clin Immunol. 2014. PMID: 24691999 Review.

10

Differences in FOXP3 and CD127 expression in Treg-like cells in patients with IPEX syndrome.

Boldt A, Kentouche K, Fricke S, Borte S, Kahlenberg F, Sack U. Boldt A, et al. Among authors: borte s. Clin Immunol. 2014 Jul;153(1):109-11. doi: 10.1016/j.clim.2014.04.001. Epub 2014 Apr 13. Clin Immunol. 2014. PMID: 24727448 No abstract available.

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