Publications by authors named "Robin Lowen"

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Benign substitution (Aα289 Arg→Gln) in the αC region of human fibrinogen.
Stephen O Brennan, Ryan L Davis, Robin Lowen, Bart Baker

Blood Cells Mol Dis· December 2010

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Deletion of five residues from the coiled coil of fibrinogen (Bbeta Asn167_Glu171del) associated with bleeding and hypodysfibrinogenemia.
Stephen O Brennan, Ryan L Davis, Robin Lowen, Anna Ruskova

Haematologica· April 2009

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Novel fibrinogen Aalpha chain mutation associated with afibrinogenaemia.
Linda Saravanan, Stephen Brennan, Peter George, Robin Lowen, Mark Kirkland

Pathology· October 2007

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Congenital hypodysfibrinogenaemia (Fibrinogen Des Moines) due to a gamma320Asp deletion at the Ca2+ binding site.
Stephen O Brennan, Ryan L Davis, Michael W Mosesson, Irene Hernandez, Robin Lowen

Thromb Haemost· August 2007

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Dysfibrinogenemia (fibrinogen Wilmington) due to a novel Aalpha chain truncation causing decreased plasma expression and impaired fibrin polymerisation.
Stephen O Brennan, Michael W Mosesson, Robin Lowen, Christopher Frantz

Thromb Haemost· July 2006

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Hypofibrinogenaemia resulting from novel single nucleotide deletion at codon Bbeta58 (3404del A) associated with thrombotic stroke in infancy.
Stephen O Brennan, Michael W Mosesson, Robin Lowen, Kevin R Siebenlist, Alison Matsunaga

Thromb Haemost· April 2006

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