Girolami B - 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

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.

5

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.

6

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.

7

Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up study.

Girolami A, Santarossa C, Cosi E, Ferrari S, Lombardi AM, Girolami B. Girolami A, et al. Among authors: girolami b. Blood Coagul Fibrinolysis. 2017 Dec;28(8):623-626. doi: 10.1097/MBC.0000000000000648. Blood Coagul Fibrinolysis. 2017. PMID: 28665815

8

Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation period.

Girolami A, Ferrari S, Cosi E, Girolami B, Randi ML. Girolami A, et al. Among authors: girolami b. J Thromb Thrombolysis. 2019 Apr;47(3):481-485. doi: 10.1007/s11239-019-01819-8. J Thromb Thrombolysis. 2019. PMID: 30694429

9

The slow but progressive disappearance of the patients with the Pro343Ser (FX Friuli) mutation.

Girolami A, Ferrari S, Girolami B, Molaro G. Girolami A, et al. Among authors: girolami b. Br J Haematol. 2020 Oct;191(2):e50-e52. doi: 10.1111/bjh.16991. Epub 2020 Aug 4. Br J Haematol. 2020. PMID: 32748957 Free article. No abstract available.

10

Pregnancy and oral contraceptives in congenital bleeding disorders of the vitamin K-dependent coagulation factors.

Girolami A, Randi ML, Ruzzon E, Lombardi AM, Girolami B, Fabris F. Girolami A, et al. Among authors: girolami b. Acta Haematol. 2006;115(1-2):58-63. doi: 10.1159/000089467. Acta Haematol. 2006. PMID: 16424651

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