Girolami A - 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

A new mutation (Arg251Trp) in the Ca2+ binding site of factor X protease domain appears to be responsible for the defect in the extrinsic pathway activation of factor X Padua.

Girolami A, Vianello F, Cabrio L, Lombardi AM. Girolami A, et al. Clin Appl Thromb Hemost. 2004 Jan;10(1):5-8. doi: 10.1177/107602960401000102. Clin Appl Thromb Hemost. 2004. PMID: 14979399 Free article.

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

Considerations on a tentative classification of FVII deficiency suited for practical clinical purposes.

Girolami A, Treleani M, Scarparo P, Bonamigo E, Lombardi AM. Girolami A, et al. Clin Appl Thromb Hemost. 2012 Nov;18(6):654-7. doi: 10.1177/1076029611434529. Epub 2012 Mar 12. Clin Appl Thromb Hemost. 2012. PMID: 22411998 Free article.

5

Myocardial infarctions and other acute coronary syndromes in rare congenital bleeding disorders: a critical analysis of all reported cases.

Girolami A, Ferrari S, Sambado L, Peroni E, Cosi E. Girolami A, et al. Clin Appl Thromb Hemost. 2015 May;21(4):359-64. doi: 10.1177/1076029614548056. Epub 2014 Aug 25. Clin Appl Thromb Hemost. 2015. PMID: 25155499 Free article. Review.

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

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

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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