Ferrari S - Search Results

1

Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T).

Girolami A, Minoldo S, Ferrari S, Colussi D, Lombardi AM, Guglielmone H. Girolami A, et al. Among authors: ferrari s. Cardiovasc Hematol Disord Drug Targets. 2017;17(2):136-141. doi: 10.2174/1871529X17666170908105839. Cardiovasc Hematol Disord Drug Targets. 2017. PMID: 28891452

2

Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is needed.

Girolami A, Ferrari S, Cosi E, Girolami B, Lombardi AM. Girolami A, et al. Among authors: ferrari s. Hematology. 2018 Mar;23(2):105-110. doi: 10.1080/10245332.2017.1359900. Epub 2017 Aug 1. Hematology. 2018. PMID: 28762299 Free article. Review.

3

A structure-function analysis in patients with prekallikrein deficiency.

Girolami A, Ferrari S, Cosi E, Lombardi AM. Girolami A, et al. Among authors: ferrari s. Hematology. 2018 Jul;23(6):346-350. doi: 10.1080/10245332.2017.1405572. Epub 2017 Nov 22. Hematology. 2018. PMID: 29165051 Free article.

4

Factor X Deficiency Due to a Compound Heterozygosis Between a New Mutation (Gla72Asp) in Exon 2 and an Already Known one (Gly154Arg) in Exon 5: Factor X Mar Del Plata1).

Girolami A, de Paoletti DNG, Nenkies ML, Ferrari S, Guglielmone H. Girolami A, et al. Among authors: ferrari s. Cardiovasc Hematol Disord Drug Targets. 2019;19(2):169-173. doi: 10.2174/1871529X19666181212103944. Cardiovasc Hematol Disord Drug Targets. 2019. PMID: 30539705

5

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: ferrari s. Cardiovasc Hematol Disord Drug Targets. 2019;19(3):233-238. doi: 10.2174/1871529X19666190308114842. Cardiovasc Hematol Disord Drug Targets. 2019. PMID: 30854979

6

A family with factor X deficiency from Argentina: a compound heterozygosis because of the combination of a new mutation (Gln138Arg) with an already known one (Glu350Lys).

Girolami A, Molina MA, Galletti ML, Ferrari S, Sambado L, Guglielmone H. Girolami A, et al. Among authors: ferrari s. Blood Coagul Fibrinolysis. 2016 Sep;27(6):732-6. doi: 10.1097/MBC.0000000000000563. Blood Coagul Fibrinolysis. 2016. PMID: 27031279

7

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: ferrari s. Eur J Haematol. 2016 Dec;97(6):547-553. doi: 10.1111/ejh.12767. Epub 2016 May 30. Eur J Haematol. 2016. PMID: 27124643

8

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: ferrari s. 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.

9

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: ferrari s. Hematology. 2017 Jul;22(6):375-379. doi: 10.1080/10245332.2017.1286540. Epub 2017 Feb 8. Hematology. 2017. PMID: 28176610 Free article.

10

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: ferrari s. Blood Coagul Fibrinolysis. 2017 Dec;28(8):623-626. doi: 10.1097/MBC.0000000000000648. Blood Coagul Fibrinolysis. 2017. PMID: 28665815

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