Pignata C - Search Results

1

Novel STAT1 gain-of-function mutation and suppurative infections.

Giardino G, Somma D, Cirillo E, Ruggiero G, Terrazzano G, Rubino V, Ursini MV, Vairo D, Badolato R, Carsetti R, Leonardi A, Puel A, Pignata C. Giardino G, et al. Among authors: pignata c. Pediatr Allergy Immunol. 2016 Mar;27(2):220-3. doi: 10.1111/pai.12496. Epub 2015 Dec 15. Pediatr Allergy Immunol. 2016. PMID: 26467763 No abstract available.

2

Brain migration disorder and T-cell activation deficiency associated with abnormal signaling through TCR/CD3 complex and hyperactivity of Fyn tyrosine kinase.

Del Giudice E, Gaetaniello L, Matrecano E, Cosentini E, Ursini MV, Racioppi L, Arrigo G, Pignata C. Del Giudice E, et al. Among authors: pignata c. Neuropediatrics. 2000 Oct;31(5):265-8. doi: 10.1055/s-2000-9234. Neuropediatrics. 2000. PMID: 11204284

3

Abnormal GH receptor signaling in children with idiopathic short stature.

Salerno M, Balestrieri B, Matrecano E, Officioso A, Rosenfeld RG, Di Maio S, Fimiani G, Ursini MV, Pignata C. Salerno M, et al. Among authors: pignata c. J Clin Endocrinol Metab. 2001 Aug;86(8):3882-8. doi: 10.1210/jcem.86.8.7759. J Clin Endocrinol Metab. 2001. PMID: 11502828

4

The structure of human STAT5A and B genes reveals two regions of nearly identical sequence and an alternative tissue specific STAT5B promoter.

Ambrosio R, Fimiani G, Monfregola J, Sanzari E, De Felice N, Salerno MC, Pignata C, D'Urso M, Ursini MV. Ambrosio R, et al. Among authors: pignata c. Gene. 2002 Feb 20;285(1-2):311-8. doi: 10.1016/s0378-1119(02)00421-3. Gene. 2002. PMID: 12039059

5

Atypical X-linked SCID phenotype associated with growth hormone hyporesponsiveness.

Ursini MV, Gaetaniello L, Ambrosio R, Matrecano E, Apicella AJ, Salerno MC, Pignata C. Ursini MV, et al. Among authors: pignata c. Clin Exp Immunol. 2002 Sep;129(3):502-9. doi: 10.1046/j.1365-2249.2002.01823.x. Clin Exp Immunol. 2002. PMID: 12197892 Free PMC article.

6

Atypical features of familial hemophagocytic lymphohistiocytosis.

Busiello R, Adriani M, Locatelli F, Galgani M, Fimiani G, Clementi R, Ursini MV, Racioppi L, Pignata C. Busiello R, et al. Among authors: pignata c. Blood. 2004 Jun 15;103(12):4610-2. doi: 10.1182/blood-2003-10-3551. Epub 2004 Jan 22. Blood. 2004. PMID: 14739222 Free article.

7

Ancestral founder mutation of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy population.

Adriani M, Martinez-Mir A, Fusco F, Busiello R, Frank J, Telese S, Matrecano E, Ursini MV, Christiano AM, Pignata C. Adriani M, et al. Among authors: pignata c. Ann Hum Genet. 2004 May;68(Pt 3):265-8. doi: 10.1046/j.1529-8817.2004.00091.x. Ann Hum Genet. 2004. PMID: 15180707

8

A91V perforin variation in healthy subjects and FHLH patients.

Busiello R, Fimiani G, Miano MG, Aricò M, Santoro A, Ursini MV, Pignata C. Busiello R, et al. Among authors: pignata c. Int J Immunogenet. 2006 Apr;33(2):123-5. doi: 10.1111/j.1744-313X.2006.00582.x. Int J Immunogenet. 2006. PMID: 16611257

9

In ataxia-teleangiectasia betamethasone response is inversely correlated to cerebellar atrophy and directly to antioxidative capacity.

Russo I, Cosentino C, Del Giudice E, Broccoletti T, Amorosi S, Cirillo E, Aloj G, Fusco A, Costanzo V, Pignata C. Russo I, et al. Among authors: pignata c. Eur J Neurol. 2009 Jun;16(6):755-9. doi: 10.1111/j.1468-1331.2009.02600.x. Eur J Neurol. 2009. PMID: 19475758

10

Altered signaling through IL-12 receptor in children with very high serum IgE levels.

Fusco A, Vigliano I, Palamaro L, Cirillo E, Aloj G, Piscopo G, Giardino G, Pignata C. Fusco A, et al. Among authors: pignata c. Cell Immunol. 2010;265(1):74-9. doi: 10.1016/j.cellimm.2010.07.005. Epub 2010 Jul 21. Cell Immunol. 2010. PMID: 20696422

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