1-4 of 4
Henry G Watson
Close
Sort by
Journal Articles

Characterizing the United Kingdom Congenital Thrombotic Thrombocytopenic Purpura Population

Ferras Alwan, MBBS, Chiara Vendramin, Ri Liesner, Tina Dutt, Amanda Clark, Jayashree Motwani, Will Lester, Vickie McDonald, Rachel Rayment, Nichola Cooper, MA, MD MRCP, FRCPath, Richard Gooding, Hamish Lyall, Tina Biss, MD, Joost van Veen, Henry G Watson, John-Paul Westwood, Mari Thomas, Marie Scully
Journal: Blood
Blood (2017) 130 (Supplement 1): 3616.
https://doi.org/10.1182/blood.V130.Suppl_1.3616.3616
Published: 2017
Journal Articles

Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9

Brief Report
Klaus Schmitz-Abe, Szymon J. Ciesielski, Paul J. Schmidt, Dean R. Campagna, Fedik Rahimov, Brenda A. Schilke, Marloes Cuijpers, Klaus Rieneck, Birgitte Lausen, Michael L. Linenberger, Anoop K. Sendamarai, Chaoshe Guo, Inga Hofmann, Peter E. Newburger, Dana Matthews, Akiko Shimamura, Pieter J. L. M. Snijders, Meghan C. Towne, Charlotte M. Niemeyer, Henry G. Watson, Morten H. Dziegiel, Matthew M. Heeney, Alison May, Sylvia S. Bottomley, Dorine W. Swinkels, Kyriacos Markianos, Elizabeth A. Craig, Mark D. Fleming
Journal: Blood
Blood (2015) 126 (25): 2734–2738.
https://doi.org/10.1182/blood-2015-09-659854
Published: 2015
Includes: Supplemental data
Journal Articles

Mapping helper T-cell epitopes on platelet membrane glycoprotein IIIa in chronic autoimmune thrombocytopenic purpura

Hosea Sukati, Henry G. Watson, Stanislaw J. Urbaniak, Robert N. Barker
Journal: Blood
Blood (2007) 109 (10): 4528–4538.
https://doi.org/10.1182/blood-2006-09-044388
Published: 2007
Journal Articles

Platelet and Coagulation Activation in Myeloproliferative Diseases (MPD), and Relationship to JAK2(V617F) Mutation Status and Clonality.

Beverley J. Robertson, Colin Urquhart, Isobel Ford, Henry G. Watson, Mark Vickers, Michael Greaves
Journal: Blood
Blood (2006) 108 (11): 4082.
https://doi.org/10.1182/blood.V108.11.4082.4082
Published: 2006