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A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss.
Stritt S, Nurden P, Turro E, Greene D, Jansen SB, Westbury SK, Petersen R, Astle WJ, Marlin S, Bariana TK, Kostadima M, Lentaigne C, Maiwald S, Papadia S, Kelly AM, Stephens JC, Penkett CJ, Ashford S, Tuna S, Austin S, Bakchoul T, Collins P, Favier R, Lambert MP, Mathias M, Millar CM, Mapeta R, Perry DJ, Schulman S, Simeoni I, Thys C; BRIDGE-BPD Consortium; Gomez K, Erber WN, Stirrups K, Rendon A, Bradley JR, van Geet C, Raymond FL, Laffan MA, Nurden AT, Nieswandt B, Richardson S, Freson K, Ouwehand WH, Mumford AD. Stritt S, et al. Among authors: laffan ma. Blood. 2016 Jun 9;127(23):2903-14. doi: 10.1182/blood-2015-10-675629. Epub 2016 Feb 24. Blood. 2016. PMID: 26912466 Free article.
Recombinant FVIIa in the management of uncontrolled hemorrhage.
O'Connell NM, Perry DJ, Hodgson AJ, O'Shaughnessy DF, Laffan MA, Smith OP. O'Connell NM, et al. Among authors: laffan ma. Transfusion. 2003 Dec;43(12):1711-6. doi: 10.1046/j.0041-1132.2003.00577.x. Transfusion. 2003. PMID: 14641868
Hunting for the mutation in inherited thrombophilia.
Gomez K, Laffan MA. Gomez K, et al. Among authors: laffan ma. Blood Coagul Fibrinolysis. 2004 Mar;15(2):125-7. doi: 10.1097/00001721-200403000-00002. Blood Coagul Fibrinolysis. 2004. PMID: 15090998 Review.
Two novel mutations in severe factor VII deficiency.
Gomez K, Laffan MA, Kemball-Cook G, Pasi J, Layton M, Singer JD, Tuddenham EG, McVey JH. Gomez K, et al. Among authors: laffan ma. Br J Haematol. 2004 Jul;126(1):105-10. doi: 10.1111/j.1365-2141.2004.04997.x. Br J Haematol. 2004. PMID: 15198740 Free article.
262 results