Girolami B - Search Results

1

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.

2

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.

3

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.

4

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

5

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.

6

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

7

Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and Thrombosis.

Girolami A, Cosi E, Ferrari S, Girolami B. Girolami A, et al. Among authors: girolami b. Clin Appl Thromb Hemost. 2018 Sep;24(6):845-849. doi: 10.1177/1076029618770741. Epub 2018 Apr 24. Clin Appl Thromb Hemost. 2018. PMID: 29690772 Free PMC article. Review.

8

Thrombotic Events in Homozygotes with a Proven or Highly Probable Arg304Gln Factor VII Mutation (FVII Padua)1): Only Limited Replacement Therapy is Needed in Case of Surgery.

Girolami A, Cosi E, Ferrari S, Girolami B, Randi ML. Girolami A, et al. Among authors: girolami b. Cardiovasc Hematol Disord Drug Targets. 2019;19(3):233-238. doi: 10.2174/1871529X19666190308114842. Cardiovasc Hematol Disord Drug Targets. 2019. PMID: 30854979

9

Increased Prevalence of Reported Cases of Congenital Prekallikrein Deficiency Among African Americans as Compared With the General Population of the United States.

Girolami A, Ferrari S, Cosi E, Girolami B. Girolami A, et al. Among authors: girolami b. Clin Appl Thromb Hemost. 2020 Jan-Dec;26:1076029620918301. doi: 10.1177/1076029620918301. Clin Appl Thromb Hemost. 2020. PMID: 32243188 Free PMC article. No abstract available.

10

Prevalence of Cardiovascular Disorders in African-Americans With Congenital Prekallikrein Deficiency Versus Caucasians-Americans With the Same Defect.

Girolami A, Ferrari S, Girolami B. Girolami A, et al. Among authors: girolami b. Clin Appl Thromb Hemost. 2020 Jan-Dec;26:1076029620972481. doi: 10.1177/1076029620972481. Clin Appl Thromb Hemost. 2020. PMID: 33176434 Free PMC article. No abstract available.

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