Fabris F - Search Results

1

Relapsing thrombotic thrombocytopenic purpura with low ADAMTS13 antigen levels: An indication for splenectomy?

Lombardi AM, Pasquale ID, Businaro MA, Cortella I, Ferrari S, Fabris F, Vianello F. Lombardi AM, et al. Among authors: fabris f. Hematol Rep. 2019 Mar 19;11(1):7904. doi: 10.4081/hr.2019.7904. eCollection 2019 Feb 19. Hematol Rep. 2019. PMID: 30996851 Free PMC article.

2

Defective ADAMTS13 synthesis as a possible consequence of NASH in an obese patient with recurrent thrombotic thrombocytopenic purpura.

Lombardi AM, Fabris R, Berti de Marinis G, Marson P, Navaglia F, Plebani M, Vettor R, Fabris F. Lombardi AM, et al. Among authors: fabris r, fabris f. Eur J Haematol. 2014 Jun;92(6):497-501. doi: 10.1111/ejh.12273. Epub 2014 Feb 20. Eur J Haematol. 2014. PMID: 24460705

3

Serum Thrombopoietin and cMpl Expression in Thrombocytopenia of Different Etiologies.

Vianello F, Vettore S, Tezza F, Toni LD, Scandellari R, Sambado L, Treleani M, Fabris F. Vianello F, et al. Among authors: fabris f. Hematol Rep. 2014 Mar 26;6(1):4996. doi: 10.4081/hr.2014.4996. eCollection 2014 Jan 29. Hematol Rep. 2014. PMID: 24711916 Free PMC article.

4

Correlation between ADAMTS13 activity and neurological impairment in acute thrombotic microangiopathy patients.

Berti de Marinis G, Novello S, Ferrari S, Barzon I, Cortella I, Businaro MA, Fabris F, Lombardi AM. Berti de Marinis G, et al. Among authors: fabris f. J Thromb Thrombolysis. 2016 Nov;42(4):586-92. doi: 10.1007/s11239-016-1395-7. J Thromb Thrombolysis. 2016. PMID: 27379499

5

New heterozygous variant in GP1BB gene is responsible for an inherited form of macrothrombocytopenia.

Ferrari S, Lombardi AM, Cortella I, Businaro MA, Bertomoro A, Di Pasquale I, Fabris F. Ferrari S, et al. Among authors: fabris f. Br J Haematol. 2019 Mar;184(5):855-858. doi: 10.1111/bjh.15176. Epub 2018 Mar 12. Br J Haematol. 2019. PMID: 29527674 Free article. No abstract available.

6

Link between von Willebrand factor multimers, relapses and coronary microcirculation in patients with thrombotic thrombocytopenic purpura in remission.

Di Pasquale I, Budde U, Tona F, Bertomoro A, Lombardi AM, Famoso G, Bertozzi I, Dittmer R, Schneppenheim S, Fabris F. Di Pasquale I, et al. Among authors: fabris f. Thromb Res. 2019 Jan;173:42-47. doi: 10.1016/j.thromres.2018.11.005. Epub 2018 Nov 12. Thromb Res. 2019. PMID: 30471507

7

Spectrum of 5'UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected.

Ferrari S, Lombardi AM, Putti MC, Bertomoro A, Cortella I, Barzon I, Girolami A, Fabris F. Ferrari S, et al. Among authors: fabris f. Platelets. 2017 Sep;28(6):621-624. doi: 10.1080/09537104.2016.1267337. Epub 2017 Feb 16. Platelets. 2017. PMID: 28277066 Free article. No abstract available.

8

Thromboses and hemorrhages are common in MPN patients with high JAK2V617F allele burden.

Bertozzi I, Bogoni G, Biagetti G, Duner E, Lombardi AM, Fabris F, Randi ML. Bertozzi I, et al. Among authors: fabris f. Ann Hematol. 2017 Aug;96(8):1297-1302. doi: 10.1007/s00277-017-3040-8. Epub 2017 Jun 6. Ann Hematol. 2017. PMID: 28585070

9

Familial acquired thrombotic thrombocytopenic purpura: immunogenetic link with HLA-DRB1*11 and DQB1*03 antigens.

Lombardi AM, Pulini S, Passeri C, Iuliani O, Salutari P, Businaro A, Fabris F, Vianello F. Lombardi AM, et al. Among authors: fabris f. Br J Haematol. 2018 Oct;183(2):317-319. doi: 10.1111/bjh.14975. Epub 2017 Oct 26. Br J Haematol. 2018. PMID: 29076136 Free article. No abstract available.

10

Relevance of antiphospholipid antibody profile in the clinical outcome of ITP: a single-centre study.

Frison L, Lombardi A, Caputo I, Semenzato G, Fabris F, Vianello F. Frison L, et al. Among authors: fabris f. Hematology. 2019 Dec;24(1):134-138. doi: 10.1080/10245332.2018.1532649. Epub 2018 Oct 25. Hematology. 2019. PMID: 30355275 Free article.

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