Tommasini A - Search Results

1

Genetic bases of C7 deficiency: systematic review and report of a novel deletion determining functional hemizygosity.

Balduit A, Bianco AM, Mangogna A, Zicari AM, Leonardi L, Cinicola BL, Capponi M, Tommasini A, Agostinis C, d'Adamo AP, Bulla R. Balduit A, et al. Among authors: tommasini a. Front Immunol. 2023 May 25;14:1192690. doi: 10.3389/fimmu.2023.1192690. eCollection 2023. Front Immunol. 2023. PMID: 37304269 Free PMC article.

2

Inflammation profile of four early onset Crohn patients.

Marcuzzi A, Girardelli M, Bianco AM, Martelossi S, Magnolato A, Tommasini A, Crovella S. Marcuzzi A, et al. Among authors: tommasini a. Gene. 2012 Feb 10;493(2):282-5. doi: 10.1016/j.gene.2011.11.043. Epub 2011 Dec 6. Gene. 2012. PMID: 22155628

3

A common genetic background could explain early-onset Crohn's disease.

Bianco AM, Zanin V, Girardelli M, Magnolato A, Martelossi S, Tommasini A, Marcuzzi A, Crovella S. Bianco AM, et al. Among authors: tommasini a. Med Hypotheses. 2012 Apr;78(4):520-2. doi: 10.1016/j.mehy.2012.01.023. Epub 2012 Feb 10. Med Hypotheses. 2012. PMID: 22309886

4

Evolutionary hypothesis of the Mevalonate Kinase Deficiency.

Vuch J, Marcuzzi A, Bianco AM, Tommasini A, Zanin V, Crovella S. Vuch J, et al. Among authors: tommasini a. Med Hypotheses. 2013 Jan;80(1):67-9. doi: 10.1016/j.mehy.2012.10.016. Epub 2012 Nov 17. Med Hypotheses. 2013. PMID: 23168296

5

Genetic and functional profiling of Crohn's disease: autophagy mechanism and susceptibility to infectious diseases.

Marcuzzi A, Bianco AM, Girardelli M, Tommasini A, Martelossi S, Monasta L, Crovella S. Marcuzzi A, et al. Among authors: tommasini a. Biomed Res Int. 2013;2013:297501. doi: 10.1155/2013/297501. Epub 2013 May 8. Biomed Res Int. 2013. PMID: 23738324 Free PMC article. Review.

6

Novel missense mutation in the NOD2 gene in a patient with early onset ulcerative colitis: causal or chance association?

Girardelli M, Vuch J, Tommasini A, Crovella S, Bianco AM. Girardelli M, et al. Among authors: tommasini a. Int J Mol Sci. 2014 Mar 3;15(3):3834-41. doi: 10.3390/ijms15033834. Int J Mol Sci. 2014. PMID: 24595243 Free PMC article.

7

F402L variant in NLRP12 in subjects with undiagnosed periodic fevers and in healthy controls.

De Pieri C, Vuch J, Athanasakis E, Severini GM, Crovella S, Bianco AM, Tommasini A. De Pieri C, et al. Among authors: tommasini a. Clin Exp Rheumatol. 2014 Nov-Dec;32(6):993-4. Epub 2014 Oct 20. Clin Exp Rheumatol. 2014. PMID: 25327218 No abstract available.

8

Genetic profiling of autoinflammatory disorders in patients with periodic fever: a prospective study.

De Pieri C, Vuch J, De Martino E, Bianco AM, Ronfani L, Athanasakis E, Bortot B, Crovella S, Taddio A, Severini GM, Tommasini A. De Pieri C, et al. Among authors: tommasini a. Pediatr Rheumatol Online J. 2015 Apr 10;13:11. doi: 10.1186/s12969-015-0006-z. eCollection 2015. Pediatr Rheumatol Online J. 2015. PMID: 25866490 Free PMC article.

9

Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results.

Bianco AM, Faletra F, Vozzi D, Girardelli M, Knowles A, Tommasini A, Zauli G, Marcuzzi A. Bianco AM, et al. Among authors: tommasini a. Mol Med Rep. 2015 Oct;12(4):6128-32. doi: 10.3892/mmr.2015.4215. Epub 2015 Aug 11. Mol Med Rep. 2015. PMID: 26300074

10

Fever tree revisited: From malaria to autoinflammatory diseases.

Pastore S, Vuch J, Bianco AM, Taddio A, Tommasini A. Pastore S, et al. Among authors: tommasini a. World J Clin Pediatr. 2015 Nov 8;4(4):106-12. doi: 10.5409/wjcp.v4.i4.106. eCollection 2015 Nov 8. World J Clin Pediatr. 2015. PMID: 26566482 Free PMC article. Review.

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