Suffritti C - Search Results

1

Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: functional and structural correlates.

Pappalardo E, Caccia S, Suffritti C, Tordai A, Zingale LC, Cicardi M. Pappalardo E, et al. Among authors: suffritti c. Mol Immunol. 2008 Aug;45(13):3536-44. doi: 10.1016/j.molimm.2008.05.007. Epub 2008 Jun 30. Mol Immunol. 2008. PMID: 18586324

2

Ongoing contact activation in patients with hereditary angioedema.

Konings J, Cugno M, Suffritti C, Ten Cate H, Cicardi M, Govers-Riemslag JW. Konings J, et al. Among authors: suffritti c. PLoS One. 2013 Aug 27;8(8):e74043. doi: 10.1371/journal.pone.0074043. eCollection 2013. PLoS One. 2013. PMID: 24013493 Free PMC article. Clinical Trial.

3

Pharmacokinetics of plasma-derived C1-esterase inhibitor after subcutaneous versus intravenous administration in subjects with mild or moderate hereditary angioedema: the PASSION study.

Martinez-Saguer I, Cicardi M, Suffritti C, Rusicke E, Aygören-Pürsün E, Stoll H, Rossmanith T, Feussner A, Kalina U, Kreuz W. Martinez-Saguer I, et al. Among authors: suffritti c. Transfusion. 2014 Jun;54(6):1552-61. doi: 10.1111/trf.12501. Epub 2013 Nov 24. Transfusion. 2014. PMID: 24266596 Free PMC article. Clinical Trial.

4

High-molecular-weight kininogen cleavage correlates with disease states in the bradykinin-mediated angioedema due to hereditary C1-inhibitor deficiency.

Suffritti C, Zanichelli A, Maggioni L, Bonanni E, Cugno M, Cicardi M. Suffritti C, et al. Clin Exp Allergy. 2014 Dec;44(12):1503-14. doi: 10.1111/cea.12293. Clin Exp Allergy. 2014. PMID: 24552232

5

Presentation, diagnosis and treatment of angioedema without wheals: a retrospective analysis of a cohort of 1058 patients.

Mansi M, Zanichelli A, Coerezza A, Suffritti C, Wu MA, Vacchini R, Stieber C, Cichon S, Cicardi M. Mansi M, et al. Among authors: suffritti c. J Intern Med. 2015 May;277(5):585-93. doi: 10.1111/joim.12304. Epub 2014 Sep 27. J Intern Med. 2015. PMID: 25196353 Free article.

6

Pathophysiology of Hereditary Angioedema.

Caccia S, Suffritti C, Cicardi M. Caccia S, et al. Among authors: suffritti c. Pediatr Allergy Immunol Pulmonol. 2014 Dec 1;27(4):159-163. doi: 10.1089/ped.2014.0425. Pediatr Allergy Immunol Pulmonol. 2014. PMID: 25538858 Free PMC article. Review.

7

Efficacy of on-demand treatment in reducing morbidity in patients with hereditary angioedema due to C1 inhibitor deficiency.

Zanichelli A, Mansi M, Azin GM, Wu MA, Periti G, Casazza G, Vacchini R, Suffritti C, Cicardi M. Zanichelli A, et al. Among authors: suffritti c. Allergy. 2015 Dec;70(12):1553-8. doi: 10.1111/all.12731. Epub 2015 Sep 30. Allergy. 2015. PMID: 26304015

8

High prevalence of splenic marginal zone lymphoma among patients with acquired C1 inhibitor deficiency.

Castelli R, Wu MA, Arquati M, Zanichelli A, Suffritti C, Rossi D, Cicardi M. Castelli R, et al. Among authors: suffritti c. Br J Haematol. 2016 Mar;172(6):902-8. doi: 10.1111/bjh.13908. Epub 2016 Jan 5. Br J Haematol. 2016. PMID: 26728240 Free article.

9

Elevated plasma levels of vascular permeability factors in C1 inhibitor-deficient hereditary angioedema.

Loffredo S, Bova M, Suffritti C, Borriello F, Zanichelli A, Petraroli A, Varricchi G, Triggiani M, Cicardi M, Marone G. Loffredo S, et al. Among authors: suffritti c. Allergy. 2016 Jul;71(7):989-96. doi: 10.1111/all.12862. Epub 2016 Mar 17. Allergy. 2016. PMID: 26873113

10

Plasmin is a natural trigger for bradykinin production in patients with hereditary angioedema with factor XII mutations.

de Maat S, Björkqvist J, Suffritti C, Wiesenekker CP, Nagtegaal W, Koekman A, van Dooremalen S, Pasterkamp G, de Groot PG, Cicardi M, Renné T, Maas C. de Maat S, et al. Among authors: suffritti c. J Allergy Clin Immunol. 2016 Nov;138(5):1414-1423.e9. doi: 10.1016/j.jaci.2016.02.021. Epub 2016 Apr 6. J Allergy Clin Immunol. 2016. PMID: 27130860

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