Brennan SO - Search Results

1

Human plasma fibrinogen is synthesized in the liver.

Tennent GA, Brennan SO, Stangou AJ, O'Grady J, Hawkins PN, Pepys MB. Tennent GA, et al. Among authors: brennan so. Blood. 2007 Mar 1;109(5):1971-4. doi: 10.1182/blood-2006-08-040956. Epub 2006 Nov 2. Blood. 2007. PMID: 17082318 Free article.

2

Hereditary amyloidosis with progressive peripheral neuropathy associated with apolipoprotein AI Gly26Arg: outcome of hepatorenal transplantation.

Testro AG, Brennan SO, Macdonell RA, Hawkins PN, Angus PW. Testro AG, et al. Among authors: brennan so. Liver Transpl. 2007 Jul;13(7):1028-31. doi: 10.1002/lt.21176. Liver Transpl. 2007. PMID: 17600344 Free article.

3

Fibrinogen Hillsborough: a novel gammaGly309Asp dysfibrinogen with impaired clotting.

Mullin JL, Brennan SO, Ganly PS, George PM. Mullin JL, et al. Among authors: brennan so. Blood. 2002 May 15;99(10):3597-601. doi: 10.1182/blood.v99.10.3597. Blood. 2002. PMID: 11986213 Free article.

4

Hypofibrinogenemia in an individual with 2 coding (gamma82 A-->G and Bbeta235 P-->L) and 2 noncoding mutations.

Brennan SO, Fellowes AP, Faed JM, George PM. Brennan SO, et al. Blood. 2000 Mar 1;95(5):1709-13. Blood. 2000. PMID: 10688828 Free article.

5

Severe hypodysfibrinogenemia in compound heterozygotes of the fibrinogen AalphaIVS4 + 1G>T mutation and an AalphaGln328 truncation (fibrinogen Keokuk).

Lefebvre P, Velasco PT, Dear A, Lounes KC, Lord ST, Brennan SO, Green D, Lorand L. Lefebvre P, et al. Among authors: brennan so. Blood. 2004 Apr 1;103(7):2571-6. doi: 10.1182/blood-2003-07-2316. Epub 2003 Nov 13. Blood. 2004. PMID: 14615374 Free article.

6

Homozygous truncation of the fibrinogen A alpha chain within the coiled coil causes congenital afibrinogenemia.

Fellowes AP, Brennan SO, Holme R, Stormorken H, Brosstad FR, George PM. Fellowes AP, et al. Among authors: brennan so. Blood. 2000 Jul 15;96(2):773-5. Blood. 2000. PMID: 10887149 Free article.

7

Novel fibrinogen mutation (gamma 313 Ser-->Asn) associated with hypofibrinogenemia in two unrelated families.

Meyer M, Bergmann F, Brennan SO. Meyer M, et al. Among authors: brennan so. Blood Coagul Fibrinolysis. 2006 Jan;17(1):63-7. doi: 10.1097/01.mbc.0000198053.73128.54. Blood Coagul Fibrinolysis. 2006. PMID: 16607083

8

Electrospray ionisation analysis of human fibrinogen.

Brennan SO. Brennan SO. Thromb Haemost. 1997 Sep;78(3):1055-8. Thromb Haemost. 1997. PMID: 9308753

9

Benign substitution (Aα289 Arg→Gln) in the αC region of human fibrinogen.

Brennan SO, Davis RL, Lowen R, Baker B. Brennan SO, et al. Blood Cells Mol Dis. 2010 Dec 15;45(4):336-7. doi: 10.1016/j.bcmd.2010.08.009. Epub 2010 Sep 25. Blood Cells Mol Dis. 2010. PMID: 20870435 No abstract available.

10

Novel fibrinogen gamma375 Arg-->Trp mutation (fibrinogen aguadilla) causes hepatic endoplasmic reticulum storage and hypofibrinogenemia.

Brennan SO, Maghzal G, Shneider BL, Gordon R, Magid MS, George PM. Brennan SO, et al. Hepatology. 2002 Sep;36(3):652-8. doi: 10.1053/jhep.2002.35063. Hepatology. 2002. PMID: 12198657

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