Brennan SO - Search Results

1

Fibrinogen naples I (B beta A68T) nonsubstrate thrombin-binding capacities.

Meh DA, Mosesson MW, Siebenlist KR, Simpson-Haidaris PJ, Brennan SO, DiOrio JP, Thompson K, Di Minno G. Meh DA, et al. Among authors: brennan so. Thromb Res. 2001 Jul 1;103(1):63-73. doi: 10.1016/s0049-3848(01)00273-0. Thromb Res. 2001. PMID: 11434947

2

The amino acid sequence in fibrin responsible for high affinity thrombin binding.

Meh DA, Siebenlist KR, Brennan SO, Holyst T, Mosesson MW. Meh DA, et al. Among authors: brennan so. Thromb Haemost. 2001 Mar;85(3):470-4. Thromb Haemost. 2001. PMID: 11307817

3

Thromboelastographic phenotypes of fibrinogen and its variants: clinical and non-clinical implications.

Galanakis DK, Neerman-Arbez M, Brennan S, Rafailovich M, Hyder L, Travlou O, Papadakis E, Manco-Johnson MJ, Henschen A, Scharrer I. Galanakis DK, et al. Thromb Res. 2014 Jun;133(6):1115-23. doi: 10.1016/j.thromres.2014.03.026. Epub 2014 Mar 11. Thromb Res. 2014. PMID: 24679643 Free article.

4

A novel mutation in the fibrinogen γ-chain 216 Gly>Glu causes hypofibrinogenemia.

Marchi R, Brennan S, Mijares ME. Marchi R, et al. Thromb Res. 2016 Nov;147:61-62. doi: 10.1016/j.thromres.2016.09.025. Epub 2016 Sep 22. Thromb Res. 2016. PMID: 27676255 No abstract available.

5

Hypodysfibrinogenaemia and thrombosis in association with a new fibrinogen γ chain with two mutations (γ114Tyr→His, and γ320Asp deleted).

Brennan SO, Chitlur M. Brennan SO, et al. Thromb Haemost. 2013 Jun;109(6):1180-2. doi: 10.1160/TH13-01-0068. Epub 2013 Mar 7. Thromb Haemost. 2013. PMID: 23467727 No abstract available.

6

A novel fibrinogen mutation: FGA g. 3057 C > T (p. Arg104 > Cys) impairs fibrinogen secretion.

Marchi R, Linares M, Rojas H, Ruiz-Sáez A, Meyer M, Casini A, Brennan SO. Marchi R, et al. Among authors: brennan so. BMC Hematol. 2017 Dec 22;17:22. doi: 10.1186/s12878-017-0086-8. eCollection 2017. BMC Hematol. 2017. PMID: 29299315 Free PMC article.

7

A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia.

Marchi R, Brennan S, Meyer M, Rojas H, Kanzler D, De Agrela M, Ruiz-Saez A. Marchi R, et al. Blood Cells Mol Dis. 2013 Mar;50(3):177-81. doi: 10.1016/j.bcmd.2012.11.010. Epub 2012 Dec 23. Blood Cells Mol Dis. 2013. PMID: 23266225

8

Hypofibrinogenaemia associated with novel Aα126Val→Asp mutation in the fibrinogen coiled coil.

Brennan SO, Brennan S, Laurie AD. Brennan SO, et al. Thromb Haemost. 2017 Oct 5;117(10):2000-2002. doi: 10.1160/TH17-04-0270. Epub 2017 Aug 17. Thromb Haemost. 2017. PMID: 28816342 No abstract available.

9

Thrombosis in association with a novel substitution (γ346Gly→Val) at an absolutely conserved site in the fibrinogen γ chain.

Brennan SO, Zebeljan D, Ho LL. Brennan SO, et al. Thromb Haemost. 2013 Apr;109(4):757-8. doi: 10.1160/TH12-11-0832. Epub 2013 Jan 24. Thromb Haemost. 2013. PMID: 23348147 No abstract available.

10

Fibrinogen Dusart presenting as recurrent thromboses in the hepatic portal system.

Shen YM, Trang V, Sarode R, Brennan S. Shen YM, et al. Blood Coagul Fibrinolysis. 2014 Jun;25(4):392-4. doi: 10.1097/MBC.0000000000000045. Blood Coagul Fibrinolysis. 2014. PMID: 24384913

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