Plebani A - Search Results

1

Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group.

Schütz K, Alecsandru D, Grimbacher B, Haddock J, Bruining A, Driessen G, de Vries E, van Hagen PM, Hartmann I, Fraioli F, Milito C, Mitrevski M, Quinti I, Serra G, Kelleher P, Loebinger M, Litzman J, Postranecka V, Thon V, Babar J, Condliffe AM, Exley A, Kumararatne D, Screaton N, Jones A, Bondioni MP, Lougaris V, Plebani A, Soresina A, Sirignano C, Spadaro G, Galal N, Gonzalez-Granado LI, Dettmer S, Stirling R, Chapel H, Lucas M, Patel S, Farber CM, Meyts I, Banerjee AK, Hackett S, Hurst JR, Warnatz K, Gathmann B, Baumann U; Chest CT in Antibody Deficiency Group. Schütz K, et al. Among authors: plebani a. J Clin Immunol. 2019 Jan;39(1):45-54. doi: 10.1007/s10875-018-0577-9. Epub 2018 Dec 13. J Clin Immunol. 2019. PMID: 30547383 Free article.

2

Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study.

Plebani A, Soresina A, Rondelli R, Amato GM, Azzari C, Cardinale F, Cazzola G, Consolini R, De Mattia D, Dell'Erba G, Duse M, Fiorini M, Martino S, Martire B, Masi M, Monafo V, Moschese V, Notarangelo LD, Orlandi P, Panei P, Pession A, Pietrogrande MC, Pignata C, Quinti I, Ragno V, Rossi P, Sciotto A, Stabile A; Italian Pediatric Group for XLA-AIEOP. Plebani A, et al. Clin Immunol. 2002 Sep;104(3):221-30. doi: 10.1006/clim.2002.5241. Clin Immunol. 2002. PMID: 12217331

3

Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency.

Soresina A, Lougaris V, Giliani S, Cardinale F, Armenio L, Cattalini M, Notarangelo LD, Plebani A. Soresina A, et al. Among authors: plebani a. Eur J Pediatr. 2002 Dec;161(12):656-9. doi: 10.1007/s00431-002-1083-9. Epub 2002 Oct 23. Eur J Pediatr. 2002. PMID: 12447665

4

Human immunoglobulin M memory B cells controlling Streptococcus pneumoniae infections are generated in the spleen.

Kruetzmann S, Rosado MM, Weber H, Germing U, Tournilhac O, Peter HH, Berner R, Peters A, Boehm T, Plebani A, Quinti I, Carsetti R. Kruetzmann S, et al. Among authors: plebani a. J Exp Med. 2003 Apr 7;197(7):939-45. doi: 10.1084/jem.20022020. J Exp Med. 2003. PMID: 12682112 Free PMC article.

5

BTK: 22 novel and 25 recurrent mutations in European patients with X-linked agammaglobulinemia.

Fiorini M, Franceschini R, Soresina A, Schumacher RF, Ugazio AG, Rossi P, Plebani A, Notarangelo LD. Fiorini M, et al. Among authors: plebani a. Hum Mutat. 2004 Mar;23(3):286. doi: 10.1002/humu.9219. Hum Mutat. 2004. PMID: 14974089

6

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

7

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.

8

The loss of IgM memory B cells correlates with clinical disease in common variable immunodeficiency.

Carsetti R, Rosado MM, Donnanno S, Guazzi V, Soresina A, Meini A, Plebani A, Aiuti F, Quinti I. Carsetti R, et al. Among authors: plebani a. J Allergy Clin Immunol. 2005 Feb;115(2):412-7. doi: 10.1016/j.jaci.2004.10.048. J Allergy Clin Immunol. 2005. PMID: 15696104

9

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

10

Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q.

Schäffer AA, Pfannstiel J, Webster AD, Plebani A, Hammarström L, Grimbacher B. Schäffer AA, et al. Among authors: plebani a. Hum Genet. 2006 Feb;118(6):725-9. doi: 10.1007/s00439-005-0101-1. Epub 2005 Nov 22. Hum Genet. 2006. PMID: 16328471 Free PMC article.

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