Plebani A - Search Results

1

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

2

Isolation of cosmid and cDNA clones in the region surrounding the BTK gene at Xq21.3-q22.

Vorechovský I, Vetrie D, Holland J, Bentley DR, Thomas K, Zhou JN, Notarangelo LD, Plebani A, Fontán G, Ochs HD, et al. Vorechovský I, et al. Among authors: plebani a. Genomics. 1994 Jun;21(3):517-24. doi: 10.1006/geno.1994.1310. Genomics. 1994. PMID: 7959728

3

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

4

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

5

Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency.

Kutukculer N, Moratto D, Aydinok Y, Lougaris V, Aksoylar S, Plebani A, Genel F, Notarangelo LD. Kutukculer N, et al. Among authors: plebani a. J Pediatr. 2003 Feb;142(2):194-6. doi: 10.1067/mpd.2003.41. J Pediatr. 2003. PMID: 12584544

6

Functional defects of dendritic cells in patients with CD40 deficiency.

Fontana S, Moratto D, Mangal S, De Francesco M, Vermi W, Ferrari S, Facchetti F, Kutukculer N, Fiorini C, Duse M, Das PK, Notarangelo LD, Plebani A, Badolato R. Fontana S, et al. Among authors: plebani a. Blood. 2003 Dec 1;102(12):4099-106. doi: 10.1182/blood-2003-04-1244. Epub 2003 Jul 31. Blood. 2003. PMID: 12893749 Free article.

7

Search for poliovirus long-term excretors among patients affected by agammaglobulinemia.

Fiore L, Plebani A, Buttinelli G, Fiore S, Donati V, Marturano J, Soresina A, Martire B, Azzari C, Nigro G, Cardinale F, Trizzino A, Pignata C, Alvisi P, Anastasio E, Bossi G, Ugazio AG. Fiore L, et al. Among authors: plebani a. Clin Immunol. 2004 Apr;111(1):98-102. doi: 10.1016/j.clim.2003.11.011. Clin Immunol. 2004. PMID: 15093557

8

A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome.

Fiorini C, Jilani S, Losi CG, Silini A, Giliani S, Ferrari S, Notarangelo LD, Plebani A, Sfar T, Helal A. Fiorini C, et al. Among authors: plebani a. Eur J Pediatr. 2004 Dec;163(12):704-8. doi: 10.1007/s00431-004-1540-8. Eur J Pediatr. 2004. PMID: 15372234

9

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

10

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

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