Casini A - Search Results

1

A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec.

Pelland-Marcotte MC, Avram AT, Néron H, Demers C, Castilloux J, Gauthier J, Neerman-Arbez M, Casini A, Rivard GE. Pelland-Marcotte MC, et al. Among authors: casini a. Haemophilia. 2024 May;30(3):858-861. doi: 10.1111/hae.15006. Epub 2024 Apr 1. Haemophilia. 2024. PMID: 38561627 No abstract available.

2

Congenital fibrinogen disorders: an update.

de Moerloose P, Casini A, Neerman-Arbez M. de Moerloose P, et al. Among authors: casini a. Semin Thromb Hemost. 2013 Sep;39(6):585-95. doi: 10.1055/s-0033-1349222. Epub 2013 Jul 12. Semin Thromb Hemost. 2013. PMID: 23852822 Review.

3

Fibrinogen geneva II: a new congenitally abnormal fibrinogen alpha chain (Gly17Asp) with a review of similar mutations resulting in abnormal knob A.

Casini A, De Maistre E, Casini-Stuppi V, Fontana P, Neerman-Arbez M, de Moerloose P. Casini A, et al. Among authors: casini stuppi v. Blood Coagul Fibrinolysis. 2014 Apr;25(3):280-2. doi: 10.1097/MBC.0000000000000039. Blood Coagul Fibrinolysis. 2014. PMID: 24389539

4

FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations.

Casini A, Lukowski S, Quintard VL, Crutu A, Zak M, Regazzoni S, de Moerloose P, Neerman-Arbez M. Casini A, et al. Thromb Res. 2014 May;133(5):868-74. doi: 10.1016/j.thromres.2014.01.022. Epub 2014 Jan 25. Thromb Res. 2014. PMID: 24560896

5

Natural history of patients with congenital dysfibrinogenemia.

Casini A, Blondon M, Lebreton A, Koegel J, Tintillier V, de Maistre E, Gautier P, Biron C, Neerman-Arbez M, de Moerloose P. Casini A, et al. Blood. 2015 Jan 15;125(3):553-61. doi: 10.1182/blood-2014-06-582866. Epub 2014 Oct 15. Blood. 2015. PMID: 25320241 Free PMC article.

6

Successful pregnancy under fibrinogen substitution in a woman with congenital afibrinogenaemia complicated by a postpartum venous thrombosis.

Lebreton A, Casini A, Alhayek R, Kouteich KL, Neerman-Arbez M, de Moerloose P. Lebreton A, et al. Among authors: casini a. Haemophilia. 2015 Jan;21(1):e108-10. doi: 10.1111/hae.12584. Epub 2014 Dec 4. Haemophilia. 2015. PMID: 25471400 No abstract available.

7

Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management.

Casini A, Neerman-Arbez M, Ariëns RA, de Moerloose P. Casini A, et al. J Thromb Haemost. 2015 Jun;13(6):909-19. doi: 10.1111/jth.12916. Epub 2015 May 2. J Thromb Haemost. 2015. PMID: 25816717 Free article. Review.

8

Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature.

Casini A, Sokollik C, Lukowski SW, Lurz E, Rieubland C, de Moerloose P, Neerman-Arbez M. Casini A, et al. Haemophilia. 2015 Nov;21(6):820-7. doi: 10.1111/hae.12719. Epub 2015 May 20. Haemophilia. 2015. PMID: 25990487

9

Clinical Features and Management of Congenital Fibrinogen Deficiencies.

Casini A, de Moerloose P, Neerman-Arbez M. Casini A, et al. Semin Thromb Hemost. 2016 Jun;42(4):366-74. doi: 10.1055/s-0036-1571339. Epub 2016 Mar 28. Semin Thromb Hemost. 2016. PMID: 27019462 Review.

10

Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders.

Neerman-Arbez M, de Moerloose P, Casini A. Neerman-Arbez M, et al. Among authors: casini a. Semin Thromb Hemost. 2016 Jun;42(4):356-65. doi: 10.1055/s-0036-1571340. Epub 2016 Mar 28. Semin Thromb Hemost. 2016. PMID: 27019463 Review.

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