Giliani S - Search Results

1

Characterization of T and B cell repertoire diversity in patients with RAG deficiency.

Lee YN, Frugoni F, Dobbs K, Tirosh I, Du L, Ververs FA, Ru H, Ott de Bruin L, Adeli M, Bleesing JH, Buchbinder D, Butte MJ, Cancrini C, Chen K, Choo S, Elfeky RA, Finocchi A, Fuleihan RL, Gennery AR, El-Ghoneimy DH, Henderson LA, Al-Herz W, Hossny E, Nelson RP, Pai SY, Patel NC, Reda SM, Soler-Palacin P, Somech R, Palma P, Wu H, Giliani S, Walter JE, Notarangelo LD. Lee YN, et al. Among authors: giliani s. Sci Immunol. 2016 Dec 16;1(6):eaah6109. doi: 10.1126/sciimmunol.aah6109. Epub 2016 Dec 16. Sci Immunol. 2016. PMID: 28783691 Free PMC article.

2

Application of molecular analysis to genetic counseling in the Wiskott-Aldrich syndrome (WAS).

Notarangelo LD, Candotti F, Parolini O, Mantuano E, Giliani S, Lanfranchi A, Albertini A. Notarangelo LD, et al. Among authors: giliani s. DNA Cell Biol. 1993 Sep;12(7):645-9. doi: 10.1089/dna.1993.12.645. DNA Cell Biol. 1993. PMID: 8397823

3

Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1).

Wengler GS, Giliani S, Fiorini M, Mella P, Mantuano E, Zanola A, Pollonini G, Eibl MM, Ugazio AG, Notarangelo LD, Parolini O. Wengler GS, et al. Among authors: giliani s. Br J Haematol. 1998 Jun;101(3):586-91. doi: 10.1046/j.1365-2141.1998.00721.x. Br J Haematol. 1998. PMID: 9633906 Free article.

4

Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome.

Facchetti F, Blanzuoli L, Vermi W, Notarangelo LD, Giliani S, Fiorini M, Fasth A, Stewart DM, Nelson DL. Facchetti F, et al. Among authors: giliani s. J Pathol. 1998 May;185(1):99-107. doi: 10.1002/(SICI)1096-9896(199805)185:1<99::AID-PATH48>3.0.CO;2-L. J Pathol. 1998. PMID: 9713366

5

Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterization.

Mella P, Imberti L, Brugnoni D, Pirovano S, Candotti F, Mazzolari E, Bettinardi A, Fiorini M, De Mattia D, Martire B, Plebani A, Notarangelo LD, Giliani S. Mella P, et al. Among authors: giliani s. Clin Immunol. 2000 Apr;95(1 Pt 1):39-50. doi: 10.1006/clim.2000.4842. Clin Immunol. 2000. PMID: 10794431

6

Missense mutations of the WASP gene cause intermittent X-linked thrombocytopenia.

Notarangelo LD, Mazza C, Giliani S, D'Aria C, Gandellini F, Ravelli C, Locatelli MG, Nelson DL, Ochs HD, Notarangelo LD. Notarangelo LD, et al. Among authors: giliani s. Blood. 2002 Mar 15;99(6):2268-9. doi: 10.1182/blood.v99.6.2268. Blood. 2002. PMID: 11877312 Free article.

7

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: giliani s. 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

8

Primary immune deficiencies unravel the molecular basis of immune response.

Notarangelo LD, Giliani S, Mazzolari E, Gulino AV. Notarangelo LD, et al. Among authors: giliani s. Rev Clin Exp Hematol. 2003 Mar;7(1):84-111. Rev Clin Exp Hematol. 2003. PMID: 14692236 Review.

9

Reconstitution of T-cell compartment after in utero stem cell transplantation: analysis of T-cell repertoire and thymic output.

Pirovano S, Notarangelo LD, Malacarne F, Mazzolari E, Porta F, Lanfranchi A, Giliani S, Zucca S, Pecorelli S, Albertini A, Ugazio AG, Imberti L. Pirovano S, et al. Among authors: giliani s. Haematologica. 2004 Apr;89(4):450-61. Haematologica. 2004. PMID: 15075079

10

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

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