Giliani SC - Search Results

1

When a Nontuberculous Mycobacterial Infection Reveals an Error of Immunity: A Single Center's Experience.

Morreale A, Dotta L, Vairo D, Bazzana T, Lougaris V, Soresina A, Plebani A, Giliani SC, Porta F, Matteelli A, Redaelli De Zinis LO, Badolato R. Morreale A, et al. Among authors: giliani sc. Pediatr Infect Dis J. 2022 May 1;41(5):427-429. doi: 10.1097/INF.0000000000003461. Pediatr Infect Dis J. 2022. PMID: 35086117

2

Combined immunodeficiencies due to defects in signal transduction: defects of the gammac-JAK3 signaling pathway as a model.

Notarangelo LD, Giliani S, Mella P, Schumacher RF, Mazza C, Savoldi G, Rodriguez-Pérez C, Badolato R, Mazzolari E, Porta F, Candotti F, Ugazio AG. Notarangelo LD, et al. Immunobiology. 2000 Aug;202(2):106-19. doi: 10.1016/s0171-2985(00)80058-3. Immunobiology. 2000. PMID: 10993286 Review.

3

Mutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgM.

Ferrari S, Giliani S, Insalaco A, Al-Ghonaium A, Soresina AR, Loubser M, Avanzini MA, Marconi M, Badolato R, Ugazio AG, Levy Y, Catalan N, Durandy A, Tbakhi A, Notarangelo LD, Plebani A. Ferrari S, et al. Proc Natl Acad Sci U S A. 2001 Oct 23;98(22):12614-9. doi: 10.1073/pnas.221456898. Proc Natl Acad Sci U S A. 2001. PMID: 11675497 Free PMC article.

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. 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

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria?

Buzi F, Badolato R, Mazza C, Giliani S, Notarangelo LD, Radetti G, Plebani A, Notarangelo LD. Buzi F, et al. J Clin Endocrinol Metab. 2003 Jul;88(7):3146-8. doi: 10.1210/jc.2002-021495. J Clin Endocrinol Metab. 2003. PMID: 12843157

6

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. Eur J Pediatr. 2004 Dec;163(12):704-8. doi: 10.1007/s00431-004-1540-8. Eur J Pediatr. 2004. PMID: 15372234

7

Hematopoietic stem cell transplantation in Omenn syndrome: a single-center experience.

Mazzolari E, Moshous D, Forino C, De Martiis D, Offer C, Lanfranchi A, Giliani S, Imberti L, Pasic S, Ugazio AG, Porta F, Notarangelo LD. Mazzolari E, et al. Bone Marrow Transplant. 2005 Jul;36(2):107-14. doi: 10.1038/sj.bmt.1705017. Bone Marrow Transplant. 2005. PMID: 15908971

8

Single-center analysis of long-term outcome after hematopoietic cell transplantation in children with congenital severe T cell immunodeficiency.

Mazzolari E, de Martiis D, Forino C, Lanfranchi A, Giliani S, Marzollo R, Airò P, Imberti L, Porta F, Notarangelo LD. Mazzolari E, et al. Immunol Res. 2009;44(1-3):4-17. doi: 10.1007/s12026-008-8022-4. Immunol Res. 2009. PMID: 18592143

9

Defect of regulatory T cells in patients with Omenn syndrome.

Cassani B, Poliani PL, Moratto D, Sobacchi C, Marrella V, Imperatori L, Vairo D, Plebani A, Giliani S, Vezzoni P, Facchetti F, Porta F, Notarangelo LD, Villa A, Badolato R. Cassani B, et al. J Allergy Clin Immunol. 2010 Jan;125(1):209-16. doi: 10.1016/j.jaci.2009.10.023. J Allergy Clin Immunol. 2010. PMID: 20109747

10

Different molecular behavior of CD40 mutants causing hyper-IgM syndrome.

Lanzi G, Ferrari S, Vihinen M, Caraffi S, Kutukculer N, Schiaffonati L, Plebani A, Notarangelo LD, Fra AM, Giliani S. Lanzi G, et al. Blood. 2010 Dec 23;116(26):5867-74. doi: 10.1182/blood-2010-03-274241. Epub 2010 Aug 11. Blood. 2010. PMID: 20702779 Free article.

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