Girolami A - Search Results

1

Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years).

Girolami A, Cosi E, Santarossa C, Ferrari S, Girolami B, Lombardi AM. Girolami A, et al. Among authors: girolami b. Eur J Haematol. 2016 Dec;97(6):547-553. doi: 10.1111/ejh.12767. Epub 2016 May 30. Eur J Haematol. 2016. PMID: 27124643

2

The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiency.

Girolami A, Candeo N, Vettore S, Lombardi AM, Girolami B. Girolami A, et al. Among authors: girolami b. J Thromb Thrombolysis. 2010 Apr;29(3):299-302. doi: 10.1007/s11239-009-0342-2. J Thromb Thrombolysis. 2010. PMID: 19412729 Review.

3

The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domain.

Girolami A, Allemand E, Scandellari R, Lombardi AM, Girolami B. Girolami A, et al. Among authors: girolami b. Hematology. 2009 Jun;14(3):177-81. doi: 10.1179/102453309X426173. Hematology. 2009. PMID: 19490765 Free article.

4

A cluster of factor XI-deficient patients due to a new mutation (Ile 436 Lys) in northeastern Italy.

Girolami A, Scarparo P, Bonamigo E, Santarossa L, Cristiani A, Moro S, Lombardi AM. Girolami A, et al. Eur J Haematol. 2012 Mar;88(3):229-36. doi: 10.1111/j.1600-0609.2011.01723.x. Epub 2011 Nov 17. Eur J Haematol. 2012. PMID: 21999818

5

Discrepant ratios of arterial vs. venous thrombosis in hemophilias A and B as compared to FVII deficiency.

Girolami A, Berti de Marinis G, Bertozzi I, Peroni E, Tasinato V, Lombardi AM. Girolami A, et al. Eur J Haematol. 2013 Aug;91(2):152-6. doi: 10.1111/ejh.12129. Epub 2013 May 24. Eur J Haematol. 2013. PMID: 23621110

6

Complex history of the discovery and characterization of congenital factor X deficiency.

Girolami A, Cosi E, Sambado L, Girolami B, Randi ML. Girolami A, et al. Among authors: girolami b. Semin Thromb Hemost. 2015 Jun;41(4):359-65. doi: 10.1055/s-0034-1544000. Epub 2015 Apr 14. Semin Thromb Hemost. 2015. PMID: 25875733 Review.

7

The Story of Serum Prothrombin Conversion Accelerator, Proconvertin, Stable Factor, Cothromboplastin, Prothrombin Accelerator or Autoprothrombin I, and Their Subsequent Merging into Factor VII.

Girolami A, Cosi E, Santarossa C, Ferrari S, Luigia Randi M. Girolami A, et al. Semin Thromb Hemost. 2015 Jun;41(4):366-73. doi: 10.1055/s-0035-1549851. Epub 2015 May 14. Semin Thromb Hemost. 2015. PMID: 25973586 Review.

8

Acquired Isolated FVII Deficiency: An Underestimated and Potentially Important Laboratory Finding.

Girolami A, Santarossa C, Cosi E, Ferrari S, Lombardi AM. Girolami A, et al. Clin Appl Thromb Hemost. 2016 Nov;22(8):705-711. doi: 10.1177/1076029615599440. Epub 2015 Aug 31. Clin Appl Thromb Hemost. 2016. PMID: 26329909 Free article. Review.

9

Factor X Friuli Coagulation Disorder: Almost 50 Years Later.

Girolami A, Cosi E, Santarossa C, Ferrari S, Girolami B, Lombardi AM. Girolami A, et al. Among authors: girolami b. Clin Appl Thromb Hemost. 2018 Jan;24(1):33-40. doi: 10.1177/1076029616686423. Epub 2016 Dec 29. Clin Appl Thromb Hemost. 2018. PMID: 28030967 Free PMC article. Review.

10

Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period.

Girolami A, Cosi E, Ferrari S, Girolami B, Lombardi AM. Girolami A, et al. Among authors: girolami b. Hematology. 2017 Jul;22(6):375-379. doi: 10.1080/10245332.2017.1286540. Epub 2017 Feb 8. Hematology. 2017. PMID: 28176610 Free article.

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