Plebani A - Search Results

1

CTLA-4 regulates human Natural Killer cell effector functions.

Lougaris V, Tabellini G, Baronio M, Patrizi O, Gazzurelli L, Mitsuiki N, Pozzi MR, Grimbacher B, Parolini S, Plebani A. Lougaris V, et al. Among authors: plebani a. Clin Immunol. 2018 Sep;194:43-45. doi: 10.1016/j.clim.2018.06.010. Epub 2018 Jun 30. Clin Immunol. 2018. PMID: 29966715 No abstract available.

2

ICOS deficiency in patients with common variable immunodeficiency.

Salzer U, Maul-Pavicic A, Cunningham-Rundles C, Urschel S, Belohradsky BH, Litzman J, Holm A, Franco JL, Plebani A, Hammarstrom L, Skrabl A, Schwinger W, Grimbacher B. Salzer U, et al. Among authors: plebani a. Clin Immunol. 2004 Dec;113(3):234-40. doi: 10.1016/j.clim.2004.07.002. Clin Immunol. 2004. PMID: 15507387

3

Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features.

Lougaris V, Badolato R, Ferrari S, Plebani A. Lougaris V, et al. Among authors: plebani a. Immunol Rev. 2005 Feb;203:48-66. doi: 10.1111/j.0105-2896.2005.00229.x. Immunol Rev. 2005. PMID: 15661021 Review.

4

Mutational analysis of human BAFF receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency.

Losi CG, Silini A, Fiorini C, Soresina A, Meini A, Ferrari S, Notarangelo LD, Lougaris V, Plebani A. Losi CG, et al. Among authors: plebani a. J Clin Immunol. 2005 Sep;25(5):496-502. doi: 10.1007/s10875-005-5637-2. J Clin Immunol. 2005. PMID: 16160919

5

Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q.

Finck A, Van der Meer JW, Schäffer AA, Pfannstiel J, Fieschi C, Plebani A, Webster AD, Hammarström L, Grimbacher B. Finck A, et al. Among authors: plebani a. Eur J Hum Genet. 2006 Jul;14(7):867-75. doi: 10.1038/sj.ejhg.5201634. Epub 2006 Apr 26. Eur J Hum Genet. 2006. PMID: 16639407

6

Mutational analysis of human BLyS in patients with common variable immunodeficiency.

Losi CG, Salzer U, Gatta R, Lougaris V, Cattaneo G, Meini A, Soresina A, Grimbacher B, Plebani A. Losi CG, et al. Among authors: plebani a. J Clin Immunol. 2006 Jul;26(4):396-9. doi: 10.1007/s10875-006-9026-2. Epub 2006 Jun 1. J Clin Immunol. 2006. PMID: 16838132

7

ICOS deficiency is associated with a severe reduction of CXCR5+CD4 germinal center Th cells.

Bossaller L, Burger J, Draeger R, Grimbacher B, Knoth R, Plebani A, Durandy A, Baumann U, Schlesier M, Welcher AA, Peter HH, Warnatz K. Bossaller L, et al. Among authors: plebani a. J Immunol. 2006 Oct 1;177(7):4927-32. doi: 10.4049/jimmunol.177.7.4927. J Immunol. 2006. PMID: 16982935

8

A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG.

Plebani A, Lougaris V, Soresina A, Meini A, Zunino F, Losi CG, Gatta R, Cattaneo G, Nespoli L, Marinoni M, Capolunghi F, Vivarelli M, Quinti I, Carsetti R. Plebani A, et al. Immunology. 2007 Jun;121(2):183-8. doi: 10.1111/j.1365-2567.2006.02556.x. Epub 2007 Feb 20. Immunology. 2007. PMID: 17313486 Free PMC article.

9

Screening of functional and positional candidate genes in families with common variable immunodeficiency.

Salzer U, Neumann C, Thiel J, Woellner C, Pan-Hammarström Q, Lougaris V, Hagena T, Jung J, Birmelin J, Du L, Metin A, Webster DA, Plebani A, Moschese V, Hammarström L, Schäffer AA, Grimbacher B. Salzer U, et al. Among authors: plebani a. BMC Immunol. 2008 Feb 7;9:3. doi: 10.1186/1471-2172-9-3. BMC Immunol. 2008. PMID: 18254984 Free PMC article.

10

Sensorineural hearing loss in primary antibody deficiency disorders.

Berlucchi M, Soresina A, Redaelli De Zinis LO, Valetti L, Valotti R, Lougaris V, Meini A, Salsi D, Nicolai P, Plebani A. Berlucchi M, et al. Among authors: plebani a. J Pediatr. 2008 Aug;153(2):293-6. doi: 10.1016/j.jpeds.2008.03.008. J Pediatr. 2008. PMID: 18639734

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