Moratto D - Search Results

1

Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity.

Lougaris V, Moratto D, Baronio M, Lorenzini T, Rossi S, Gazzurelli L, Bondioni MP, Plebani A. Lougaris V, et al. Among authors: moratto d. Clin Immunol. 2019 Aug;205:153-155. doi: 10.1016/j.clim.2018.11.014. Epub 2018 Nov 28. Clin Immunol. 2019. PMID: 30500415

2

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: moratto d. J Pediatr. 2003 Feb;142(2):194-6. doi: 10.1067/mpd.2003.41. J Pediatr. 2003. PMID: 12584544

3

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: moratto d. 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.

4

Combined decrease of defined B and T cell subsets in a group of common variable immunodeficiency patients.

Moratto D, Gulino AV, Fontana S, Mori L, Pirovano S, Soresina A, Meini A, Imberti L, Notarangelo LD, Plebani A, Badolato R. Moratto D, et al. Clin Immunol. 2006 Nov;121(2):203-14. doi: 10.1016/j.clim.2006.07.003. Epub 2006 Sep 7. Clin Immunol. 2006. PMID: 16962827

5

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. Among authors: moratto d. 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

6

Simultaneous quantification of recent thymic T-cell and bone marrow B-cell emigrants in patients with primary immunodeficiency undergone to stem cell transplantation.

Sottini A, Ghidini C, Zanotti C, Chiarini M, Caimi L, Lanfranchi A, Moratto D, Porta F, Imberti L. Sottini A, et al. Among authors: moratto d. Clin Immunol. 2010 Aug;136(2):217-27. doi: 10.1016/j.clim.2010.04.005. Epub 2010 May 10. Clin Immunol. 2010. PMID: 20452829

7

Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients.

Tassone L, Moratto D, Vermi W, De Francesco M, Notarangelo LD, Porta F, Lougaris V, Facchetti F, Plebani A, Badolato R. Tassone L, et al. Among authors: moratto d. Blood. 2010 Dec 2;116(23):4870-3. doi: 10.1182/blood-2010-03-272096. Epub 2010 Aug 24. Blood. 2010. PMID: 20736454 Free article.

8

SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function.

Giacomelli M, Tamassia N, Moratto D, Bertolini P, Ricci G, Bertulli C, Plebani A, Cassatella M, Bazzoni F, Badolato R. Giacomelli M, et al. Among authors: moratto d. Eur J Immunol. 2011 Oct;41(10):3075-84. doi: 10.1002/eji.201141721. Epub 2011 Sep 6. Eur J Immunol. 2011. PMID: 21792878 Free article.

9

A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP.

Lanzi G, Moratto D, Vairo D, Masneri S, Delmonte O, Paganini T, Parolini S, Tabellini G, Mazza C, Savoldi G, Montin D, Martino S, Tovo P, Pessach IM, Massaad MJ, Ramesh N, Porta F, Plebani A, Notarangelo LD, Geha RS, Giliani S. Lanzi G, et al. Among authors: moratto d. J Exp Med. 2012 Jan 16;209(1):29-34. doi: 10.1084/jem.20110896. Epub 2012 Jan 9. J Exp Med. 2012. PMID: 22231303 Free PMC article.

10

Prenatal presentation and postnatal evolution of a patient with Jansen metaphyseal dysplasia with a novel missense mutation in PTH1R.

Savoldi G, Izzi C, Signorelli M, Bondioni MP, Romani C, Lanzi G, Moratto D, Verdoni L, Pinotti M, Prefumo F, Superti-Furga A, Pilotta A. Savoldi G, et al. Among authors: moratto d. Am J Med Genet A. 2013 Oct;161A(10):2614-9. doi: 10.1002/ajmg.a.36115. Epub 2013 Aug 15. Am J Med Genet A. 2013. PMID: 23950054

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