Giliani S - Search Results

1

Adult-onset manifestation of idiopathic T-cell lymphopenia due to a heterozygous RAG1 mutation.

Abraham RS, Recher M, Giliani S, Walter JE, Lee YN, Frugoni F, Maddox DE, Kirmani S, Notarangelo LD. Abraham RS, et al. Among authors: giliani s. J Allergy Clin Immunol. 2013 May;131(5):1421-3. doi: 10.1016/j.jaci.2012.09.016. Epub 2012 Nov 2. J Allergy Clin Immunol. 2013. PMID: 23122631 Free PMC article. No abstract available.

2

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

3

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.

4

Damaging-agent sensitivity of Artemis-deficient cell lines.

Musio A, Marrella V, Sobacchi C, Rucci F, Fariselli L, Giliani S, Lanzi G, Notarangelo LD, Delia D, Colombo R, Vezzoni P, Villa A. Musio A, et al. Among authors: giliani s. Eur J Immunol. 2005 Apr;35(4):1250-6. doi: 10.1002/eji.200425555. Eur J Immunol. 2005. PMID: 15770702 Free article.

5

Omenn syndrome in an infant with IL7RA gene mutation.

Giliani S, Bonfim C, de Saint Basile G, Lanzi G, Brousse N, Koliski A, Malvezzi M, Fischer A, Notarangelo LD, Le Deist F. Giliani S, et al. J Pediatr. 2006 Feb;148(2):272-4. doi: 10.1016/j.jpeds.2005.10.004. J Pediatr. 2006. PMID: 16492442

6

Lack of iNKT cells in patients with combined immune deficiency due to hypomorphic RAG mutations.

Matangkasombut P, Pichavant M, Saez DE, Giliani S, Mazzolari E, Finocchi A, Villa A, Sobacchi C, Cortes P, Umetsu DT, Notarangelo LD. Matangkasombut P, et al. Among authors: giliani s. Blood. 2008 Jan 1;111(1):271-4. doi: 10.1182/blood-2007-06-096487. Epub 2007 Sep 21. Blood. 2008. PMID: 17890453 Free PMC article.

7

Immunodeficiencies due to defects of class-switch recombination.

Notarangelo LD, Lanzi G, Toniati P, Giliani S. Notarangelo LD, et al. Among authors: giliani s. Immunol Res. 2007;38(1-3):68-77. doi: 10.1007/s12026-007-0023-1. Immunol Res. 2007. PMID: 17917012

8

Variability of clinical and laboratory features among patients with ribonuclease mitochondrial RNA processing endoribonuclease gene mutations.

Kavadas FD, Giliani S, Gu Y, Mazzolari E, Bates A, Pegoiani E, Roifman CM, Notarangelo LD. Kavadas FD, et al. Among authors: giliani s. J Allergy Clin Immunol. 2008 Dec;122(6):1178-84. doi: 10.1016/j.jaci.2008.07.036. Epub 2008 Sep 19. J Allergy Clin Immunol. 2008. PMID: 18804272

9

Cartilage-hair hypoplasia: molecular basis and heterogeneity of the immunological phenotype.

Notarangelo LD, Roifman CM, Giliani S. Notarangelo LD, et al. Among authors: giliani s. Curr Opin Allergy Clin Immunol. 2008 Dec;8(6):534-9. doi: 10.1097/ACI.0b013e328310fe7d. Curr Opin Allergy Clin Immunol. 2008. PMID: 18978468 Review.

10

Novel presentation of Omenn syndrome in association with aniridia.

Sheehan WJ, Delmonte OM, Miller DT, Roberts AE, Bonilla FA, Morra M, Giliani S, Pai SY, Notarangelo LD, Oettgen HC. Sheehan WJ, et al. Among authors: giliani s. J Allergy Clin Immunol. 2009 Apr;123(4):966-9. doi: 10.1016/j.jaci.2008.12.007. J Allergy Clin Immunol. 2009. PMID: 19178939 Free PMC article.

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