Fasulo MR - Search Results

1

Hypercoagulability in splenectomized thalassemic patients detected by whole-blood thromboelastometry, but not by thrombin generation in platelet-poor plasma.

Tripodi A, Cappellini MD, Chantarangkul V, Padovan L, Fasulo MR, Marcon A, Mannucci PM. Tripodi A, et al. Among authors: fasulo mr. Haematologica. 2009 Nov;94(11):1520-7. doi: 10.3324/haematol.2009.010546. Epub 2009 Jul 31. Haematologica. 2009. PMID: 19648162 Free PMC article.

2

The thrombin generation assay distinguishes inhibitor from non-inhibitor patients with severe haemophilia A.

Mancuso ME, Chantarangkul V, Clerici M, Fasulo MR, Padovan L, Scalambrino E, Peyvandi F, Tripodi A, Santagostino E. Mancuso ME, et al. Among authors: fasulo mr. Haemophilia. 2016 Jul;22(4):e286-91. doi: 10.1111/hae.12927. Epub 2016 May 11. Haemophilia. 2016. PMID: 27166132

3

Low thrombin generation during major orthopaedic surgery fails to predict the bleeding risk in inhibitor patients treated with bypassing agents.

Mancuso ME, Chantarangkul V, Clerici M, Fasulo MR, Padovan L, Scalambrino E, Peyvandi F, Tripodi A, Santagostino E. Mancuso ME, et al. Among authors: fasulo mr. Haemophilia. 2016 Jul;22(4):e292-300. doi: 10.1111/hae.12939. Epub 2016 May 16. Haemophilia. 2016. PMID: 27197961

4

Novel human pathological mutations. Gene symbol: HBA2. Disease: Thalassemia alpha.

Refaldi C, Fasulo MR, Cesaretti C, Cappellini MD. Refaldi C, et al. Among authors: fasulo mr. Hum Genet. 2009 Aug;126(2):342. Hum Genet. 2009. PMID: 19694027 No abstract available.

5

Novel human pathological mutations. Gene symbol: HBB. Disease: haemoglobin variant.

Refaldi C, Cesaretti C, Fasulo MR, Cappellini MD. Refaldi C, et al. Among authors: fasulo mr. Hum Genet. 2009 Aug;126(2):343. Hum Genet. 2009. PMID: 19694029 No abstract available.

6

Absence of cardiac siderosis despite hepatic iron overload in Italian patients with thalassemia intermedia: an MRI T2* study.

Roghi A, Cappellini MD, Wood JC, Musallam KM, Patrizia P, Fasulo MR, Cesaretti C, Taher AT. Roghi A, et al. Among authors: fasulo mr. Ann Hematol. 2010 Jun;89(6):585-9. doi: 10.1007/s00277-009-0879-3. Epub 2009 Dec 17. Ann Hematol. 2010. PMID: 20016898

7

Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittent.

Di Pierro E, Besana V, Brancaleoni V, Fasulo MR, Cesaretti C, Cappellini MD. Di Pierro E, et al. Among authors: fasulo mr. Hum Genet. 2009 Apr;125(3):347. Hum Genet. 2009. PMID: 19320027 No abstract available.

8

Overview on practices in thalassemia intermedia management aiming for lowering complication rates across a region of endemicity: the OPTIMAL CARE study.

Taher AT, Musallam KM, Karimi M, El-Beshlawy A, Belhoul K, Daar S, Saned MS, El-Chafic AH, Fasulo MR, Cappellini MD. Taher AT, et al. Among authors: fasulo mr. Blood. 2010 Mar 11;115(10):1886-92. doi: 10.1182/blood-2009-09-243154. Epub 2009 Dec 23. Blood. 2010. PMID: 20032507 Free article.

9

Thrombin Generation Assay as a Laboratory Monitoring Tool during Bypassing Therapy in Patients with Hemophilia and Inhibitors.

Mancuso ME, Fasulo MR. Mancuso ME, et al. Among authors: fasulo mr. Semin Thromb Hemost. 2016 Feb;42(1):30-5. doi: 10.1055/s-0035-1564842. Epub 2015 Nov 23. Semin Thromb Hemost. 2016. PMID: 26595153 Review.

10

Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients.

Gorski MM, Blighe K, Lotta LA, Pappalardo E, Garagiola I, Mancini I, Mancuso ME, Fasulo MR, Santagostino E, Peyvandi F. Gorski MM, et al. Among authors: fasulo mr. Blood. 2016 Jun 9;127(23):2924-33. doi: 10.1182/blood-2015-12-685735. Epub 2016 Apr 8. Blood. 2016. PMID: 27060170 Free article.

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