Hammarström L - Search Results

1

Rare mutations in TNFRSF13B increase the risk of asthma symptoms in Swedish children.

Janzi M, Melén E, Kull I, Wickman M, Hammarström L. Janzi M, et al. Among authors: hammarstrom l. Genes Immun. 2012 Jan;13(1):59-65. doi: 10.1038/gene.2011.55. Epub 2011 Aug 18. Genes Immun. 2012. PMID: 21850030

2

The higher frequency of IgA deficiency among Swedish twins is not explained by HLA haplotypes.

Frankowiack M, Kovanen RM, Repasky GA, Lim CK, Song C, Pedersen NL, Hammarström L. Frankowiack M, et al. Among authors: hammarstrom l. Genes Immun. 2015 Apr-May;16(3):199-205. doi: 10.1038/gene.2014.78. Epub 2015 Jan 8. Genes Immun. 2015. PMID: 25569265

3

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.

Salzer U, Chapel HM, Webster AD, Pan-Hammarström Q, Schmitt-Graeff A, Schlesier M, Peter HH, Rockstroh JK, Schneider P, Schäffer AA, Hammarström L, Grimbacher B. Salzer U, et al. Among authors: hammarstrom l. Nat Genet. 2005 Aug;37(8):820-8. doi: 10.1038/ng1600. Epub 2005 Jul 10. Nat Genet. 2005. PMID: 16007087

4

[Ataxia-telangiectasia surveyed in Sweden].

Lähdesmäki A, Arinbjarnarson K, Arvidsson J, el Segaier M, Fasth A, Fernell E, Gustafsson D, Oxelius VA, Risberg K, Yuen J, Zetterlund P, von Zweigbergk M, Ahsgren I, Hammarström L. Lähdesmäki A, et al. Among authors: hammarstrom l. Lakartidningen. 2000 Oct 4;97(40):4461-5, 4467. Lakartidningen. 2000. PMID: 11068401 Swedish.

5

Does IgG therapy prevent Alzheimer's disease?

Hammarström L, Hansen S, Gardulf A. Hammarström L, et al. J Neuroimmunol. 2009 Oct 30;215(1-2):122-4. doi: 10.1016/j.jneuroim.2009.07.012. Epub 2009 Sep 1. J Neuroimmunol. 2009. PMID: 19726091 No abstract available.

6

Normalized immunoglobulin patterns in adults with recurrent acute otitis media and low IgG2 levels during early childhood.

Krakau M, Dagöö BR, Hammarström L, Granath A. Krakau M, et al. Among authors: hammarstrom l. Int J Pediatr Otorhinolaryngol. 2014 Jul;78(7):1153-7. doi: 10.1016/j.ijporl.2014.04.039. Epub 2014 May 2. Int J Pediatr Otorhinolaryngol. 2014. PMID: 24837869

7

The autoimmune spectrum of myasthenia gravis: a Swedish population-based study.

Fang F, Sveinsson O, Thormar G, Granqvist M, Askling J, Lundberg IE, Ye W, Hammarström L, Pirskanen R, Piehl F. Fang F, et al. Among authors: hammarstrom l. J Intern Med. 2015 May;277(5):594-604. doi: 10.1111/joim.12310. Epub 2014 Nov 13. J Intern Med. 2015. PMID: 25251578 Free article.

8

A putative susceptibility locus on chromosome 18 is not a major contributor to human selective IgA deficiency: evidence from meiotic mapping of 83 multiple-case families.

Vorechovský I, Blennow E, Nordenskjöld M, Webster AD, Hammarström L. Vorechovský I, et al. Among authors: hammarstrom l. J Immunol. 1999 Aug 15;163(4):2236-42. J Immunol. 1999. PMID: 10438966

9

The shared CTLA4-ICOS risk locus in celiac disease, IgA deficiency and common variable immunodeficiency.

Haimila K, Einarsdottir E, de Kauwe A, Koskinen LL, Pan-Hammarström Q, Kaartinen T, Kurppa K, Ziberna F, Not T, Vatta S, Ventura A, Korponay-Szabo IR, Adány R, Pocsai Z, Széles G, Dukes E, Kaukinen K, Mäki M, Koskinen S, Partanen J, Hammarström L, Saavalainen P. Haimila K, et al. Among authors: hammarstrom l. Genes Immun. 2009 Mar;10(2):151-61. doi: 10.1038/gene.2008.89. Epub 2008 Nov 20. Genes Immun. 2009. PMID: 19020530

10

Family and linkage study of selective IgA deficiency and common variable immunodeficiency.

Vorechovský I, Zetterquist H, Paganelli R, Koskinen S, Webster AD, Björkander J, Smith CI, Hammarström L. Vorechovský I, et al. Among authors: hammarstrom l. Clin Immunol Immunopathol. 1995 Nov;77(2):185-92. doi: 10.1006/clin.1995.1142. Clin Immunol Immunopathol. 1995. PMID: 7586726

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