Di Matteo G - Search Results

1

Structural defects and variations in the HIV-1 nef gene from rapid, slow and non-progressor children.

Casartelli N, Di Matteo G, Argentini C, Cancrini C, Bernardi S, Castelli G, Scarlatti G, Plebani A, Rossi P, Doria M. Casartelli N, et al. Among authors: di matteo g. AIDS. 2003 Jun 13;17(9):1291-301. doi: 10.1097/00002030-200306130-00003. AIDS. 2003. PMID: 12799550

2

CD4 and major histocompatibility complex class I downregulation by the human immunodeficiency virus type 1 nef protein in pediatric AIDS progression.

Casartelli N, Di Matteo G, Potestà M, Rossi P, Doria M. Casartelli N, et al. Among authors: di matteo g. J Virol. 2003 Nov;77(21):11536-45. doi: 10.1128/jvi.77.21.11536-11545.2003. J Virol. 2003. PMID: 14557639 Free PMC article.

3

Insight into B cell development and differentiation.

Moschese V, Orlandi P, Di Matteo G, Chini L, Carsetti R, Di Cesare S, Rossi P. Moschese V, et al. Among authors: di matteo g, di cesare s. Acta Paediatr Suppl. 2004 May;93(445):48-51. doi: 10.1111/j.1651-2227.2004.tb03056.x. Acta Paediatr Suppl. 2004. PMID: 15176720

4

Nuclear factor kappaB activity is increased in peripheral blood mononuclear cells of children affected by atopic and non-atopic eczema.

Angelini F, Di Matteo G, Balestrero S, Brunetti E, Mancino G, Rossi P, Galli E. Angelini F, et al. Among authors: di matteo g. Int J Immunopathol Pharmacol. 2007 Jan-Mar;20(1):59-67. doi: 10.1177/039463200702000107. Int J Immunopathol Pharmacol. 2007. PMID: 17346428 Free article.

5

Identification of a Btk mutation in a dysgammaglobulinemic patient with reduced B cells: XLA diagnosis or not?

Graziani S, Di Matteo G, Benini L, Di Cesare S, Chiriaco M, Chini L, Chianca M, De Iorio F, La Rocca M, Iannini R, Corrente S, Rossi P, Moschese V. Graziani S, et al. Among authors: di matteo g, di cesare s. Clin Immunol. 2008 Sep;128(3):322-8. doi: 10.1016/j.clim.2008.05.012. Clin Immunol. 2008. PMID: 18708023

6

Identification of deletion carriers in X-linked chronic granulomatous disease by real-time PCR.

Chiriaco M, Di Matteo G, Sinibaldi C, Giardina E, Nardone AM, Folgori L, D'Argenio P, Rossi P, Finocchi A. Chiriaco M, et al. Among authors: di matteo g. Genet Test Mol Biomarkers. 2009 Dec;13(6):785-9. doi: 10.1089/gtmb.2009.0074. Genet Test Mol Biomarkers. 2009. PMID: 19839755

7

Immune deficiency caused by impaired expression of nuclear factor-kappaB essential modifier (NEMO) because of a mutation in the 5' untranslated region of the NEMO gene.

Mooster JL, Cancrini C, Simonetti A, Rossi P, Di Matteo G, Romiti ML, Di Cesare S, Notarangelo L, Geha RS, McDonald DR. Mooster JL, et al. Among authors: di matteo g, di cesare s. J Allergy Clin Immunol. 2010 Jul;126(1):127-32.e7. doi: 10.1016/j.jaci.2010.04.026. Epub 2010 Jun 12. J Allergy Clin Immunol. 2010. PMID: 20542322 Free PMC article.

8

The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood.

Barroeta Seijas AB, Graziani S, Cancrini C, Finocchi A, Ferrari S, Miniero R, Conti F, Zuntini R, Chini L, Chiarello P, Bengala M, Rossi P, Moschese V, Di Matteo G. Barroeta Seijas AB, et al. Among authors: di matteo g. Int J Immunopathol Pharmacol. 2012 Apr-Jun;25(2):407-14. doi: 10.1177/039463201202500210. Int J Immunopathol Pharmacol. 2012. PMID: 22697072 Free article.

9

Chronic granulomatous disease presenting with salmonella brain abscesses.

Finocchi A, Claps A, Serafinelli J, Salfa I, Longo D, Di Matteo G, Aiuti A, Rossi P. Finocchi A, et al. Among authors: di matteo g. Pediatr Infect Dis J. 2014 May;33(5):525-8. doi: 10.1097/INF.0000000000000270. Pediatr Infect Dis J. 2014. PMID: 24445825

10

The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant.

Bellacchio E, Palma A, Corrente S, Di Girolamo F, Helen Kemp E, Di Matteo G, Comelli L, Carsetti R, Cascioli S, Cancrini C, Fierabracci A. Bellacchio E, et al. Among authors: di matteo g, di girolamo f. Gene. 2014 Oct 10;549(2):286-94. doi: 10.1016/j.gene.2014.07.064. Epub 2014 Jul 25. Gene. 2014. PMID: 25068407

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