Freiberger T - Search Results

1

Neutrophils Are Dysregulated in Patients with Hereditary Angioedema Types I and II in a Symptom-Free Period.

Grymova T, Vlkova M, Soucek P, Hakl R, Nechvatalova J, Slanina P, Stichova J, Litzman J, Freiberger T. Grymova T, et al. Among authors: freiberger t. Mediators Inflamm. 2019 May 19;2019:9515628. doi: 10.1155/2019/9515628. eCollection 2019. Mediators Inflamm. 2019. PMID: 31236065 Free PMC article.

2

Five novel mutations in the C1 inhibitor gene (C1NH) leading to a premature stop codon in patients with type I hereditary angioedema.

Freiberger T, Kolárová L, Mejstrík P, Vyskocilová M, Kuklínek P, Litzman J. Freiberger T, et al. Hum Mutat. 2002 Apr;19(4):461. doi: 10.1002/humu.9029. Hum Mutat. 2002. PMID: 11933207

3

Exon 1 polymorphism of the B2BKR gene does not influence the clinical status of patients with hereditary angioedema.

Freiberger T, Vyskocilová M, Kolárová L, Kuklínek P, Krystůfková O, Lahodná M, Hanzlíková J, Litzman J. Freiberger T, et al. Hum Immunol. 2002 Jun;63(6):492-4. doi: 10.1016/s0198-8859(02)00397-x. Hum Immunol. 2002. PMID: 12039525

4

Early manifestation and recognition of C2 complement deficiency in the form of pyogenic infection in infancy.

Litzman J, Freiberger T, Bartonková D, Vlková M, Thon V, Lokaj J. Litzman J, et al. Among authors: freiberger t. J Paediatr Child Health. 2003 May-Jun;39(4):274-7. doi: 10.1046/j.1440-1754.2003.00128.x. J Paediatr Child Health. 2003. PMID: 12755933

5

[Role of aspartic acid at position 57 of the HLA-DQ beta chain in sporadic and familial forms of selective IgA deficiency].

Freiberger T, Litzman J, Vondrusková E. Freiberger T, et al. Cas Lek Cesk. 2001 Dec 6;140(24):770-3. Cas Lek Cesk. 2001. PMID: 14655281 Czech.

6

Mannose-binding lectin gene polymorphic variants predispose to the development of bronchopulmonary complications but have no influence on other clinical and laboratory symptoms or signs of common variable immunodeficiency.

Litzman J, Freiberger T, Grimbacher B, Gathmann B, Salzer U, Pavlík T, Vlcek J, Postránecká V, Trávnícková Z, Thon V. Litzman J, et al. Among authors: freiberger t. Clin Exp Immunol. 2008 Sep;153(3):324-30. doi: 10.1111/j.1365-2249.2008.03700.x. Epub 2008 Jul 11. Clin Exp Immunol. 2008. PMID: 18637104 Free PMC article.

7

No association of FCRN promoter VNTR polymorphism with the rate of maternal-fetal IgG transfer.

Freiberger T, Ravcuková B, Grodecká L, Kurecová B, Jarkovský J, Bartonková D, Thon V, Litzman J. Freiberger T, et al. J Reprod Immunol. 2010 Jun;85(2):193-7. doi: 10.1016/j.jri.2010.04.002. Epub 2010 May 7. J Reprod Immunol. 2010. PMID: 20452034

8

Association of FcRn expression with lung abnormalities and IVIG catabolism in patients with common variable immunodeficiency.

Freiberger T, Grodecká L, Ravcuková B, Kurecová B, Postránecká V, Vlcek J, Jarkovský J, Thon V, Litzman J. Freiberger T, et al. Clin Immunol. 2010 Sep;136(3):419-25. doi: 10.1016/j.clim.2010.05.006. Clin Immunol. 2010. PMID: 20627700

9

Monitoring of CD38high expression in peripheral blood CD8+ lymphocytes in patients after kidney transplantation as a marker of cytomegalovirus infection.

Ticha O, Stouracova M, Kuman M, Studenik P, Freiberger T, Litzman J. Ticha O, et al. Among authors: freiberger t. Transpl Immunol. 2010 Oct;24(1):50-6. doi: 10.1016/j.trim.2010.10.002. Epub 2010 Oct 14. Transpl Immunol. 2010. PMID: 20951204

10

No evidence for linkage between the hereditary angiooedema clinical phenotype and the BDKR1, BDKR2, ACE or MBL2 gene.

Freiberger T, Grombiříková H, Ravčuková B, Jarkovský J, Kuklínek P, Kryštůfková O, Hanzlíková J, Daňková E, Kopecký O, Zachová R, Lahodná M, Vašáková M, Grodecká L, Litzman J. Freiberger T, et al. Scand J Immunol. 2011 Jul;74(1):100-6. doi: 10.1111/j.1365-3083.2011.02547.x. Scand J Immunol. 2011. PMID: 21375555 Free article.

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