Hammarström L - Search Results

1

Long-Term Follow-Up of Newborns with 22q11 Deletion Syndrome and Low TRECs.

Framme JL, Lundqvist C, Lundell AC, van Schouwenburg PA, Lemarquis AL, Thörn K, Lindgren S, Gudmundsdottir J, Lundberg V, Degerman S, Zetterström RH, Borte S, Hammarström L, Telemo E, Hultdin M, van der Burg M, Fasth A, Oskarsdóttir S, Ekwall O. Framme JL, et al. Among authors: hammarstrom l. J Clin Immunol. 2022 Apr;42(3):618-633. doi: 10.1007/s10875-021-01201-5. Epub 2022 Jan 26. J Clin Immunol. 2022. PMID: 35080750 Free PMC article.

2

Novel mutations in TACI (TNFRSF13B) causing common variable immunodeficiency.

Mohammadi J, Liu C, Aghamohammadi A, Bergbreiter A, Du L, Lu J, Rezaei N, Amirzargar AA, Moin M, Salzer U, Pan-Hammarström Q, Hammarström L. Mohammadi J, et al. Among authors: hammarstrom l. J Clin Immunol. 2009 Nov;29(6):777-85. doi: 10.1007/s10875-009-9317-5. Epub 2009 Jul 23. J Clin Immunol. 2009. PMID: 19629655

3

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: hammarstrom l. 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.

4

IgA deficiency and the MHC: assessment of relative risk and microheterogeneity within the HLA A1 B8, DR3 (8.1) haplotype.

Mohammadi J, Ramanujam R, Jarefors S, Rezaei N, Aghamohammadi A, Gregersen PK, Hammarström L. Mohammadi J, et al. Among authors: hammarstrom l. J Clin Immunol. 2010 Jan;30(1):138-43. doi: 10.1007/s10875-009-9336-2. Epub 2009 Oct 16. J Clin Immunol. 2010. PMID: 19834793

5

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: hammarstrom l. 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.

6

Newborn screening for primary immunodeficiencies: beyond SCID and XLA.

Borte S, Wang N, Oskarsdóttir S, von Döbeln U, Hammarström L. Borte S, et al. Among authors: hammarstrom l. 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

7

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. Among authors: hammarstrom l. PLoS One. 2012;7(8):e43419. doi: 10.1371/journal.pone.0043419. Epub 2012 Aug 16. PLoS One. 2012. PMID: 22916257 Free PMC article.

8

Guidelines for newborn screening of primary immunodeficiency diseases.

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

9

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: hammarstrom l. 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.

10

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: hammarstrom l. 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

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