Search details
1.
Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects.
Blood
; 122(25): 4090-3, 2013 Dec 12.
Article
in English
| MEDLINE | ID: mdl-24100448
2.
Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel.
Blood
; 120(25): 5041-9, 2012 Dec 13.
Article
in English
| MEDLINE | ID: mdl-23002116
3.
Identification and characterization of a novel P2Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study.
Blood
; 113(17): 4110-3, 2009 Apr 23.
Article
in English
| MEDLINE | ID: mdl-19237732
4.
Haemostatic problems in acute promyelocytic leukaemia.
Blood Rev
; 20(6): 289-97, 2006 Nov.
Article
in English
| MEDLINE | ID: mdl-16757074
5.
The incidence of lymphoma in the UK haemophilia population between 1978 and 1999.
AIDS
; 16(13): 1803-7, 2002 Sep 06.
Article
in English
| MEDLINE | ID: mdl-12218393
6.
The impact of HIV on mortality rates in the complete UK haemophilia population.
AIDS
; 18(3): 525-33, 2004 Feb 20.
Article
in English
| MEDLINE | ID: mdl-15090806
7.
A novel thromboxane A2 receptor N42S variant results in reduced surface expression and platelet dysfunction.
Thromb Haemost
; 111(5): 923-32, 2014 May 05.
Article
in English
| MEDLINE | ID: mdl-24452735
8.
Unique heterozygous intron 22 inversion band pattern in a haemophilic male detected by long polymerase chain reaction (PCR).
Thromb Haemost
; 99(4): 774-5, 2008 Apr.
Article
in English
| MEDLINE | ID: mdl-18392336
9.
Von Willebrand disease.
Clin Med (Lond)
; 7(6): 629-32, 2007 Dec.
Article
in English
| MEDLINE | ID: mdl-18193717
10.
Pregnancy in platelet-type VWD: a case series.
Thromb Haemost
; 106(2): 386-7, 2011 Aug.
Article
in English
| MEDLINE | ID: mdl-21614417
11.
Distinguishing between type 2B and pseudo-von Willebrand disease and its clinical importance.
Br J Haematol
; 133(6): 664-6, 2006 Jun.
Article
in English
| MEDLINE | ID: mdl-16704444
12.
Inherited and de novo von Willebrand disease 'Vicenza' in UK families with the R1205H mutation: diagnostic pitfalls and new insights.
Br J Haematol
; 135(1): 91-6, 2006 Oct.
Article
in English
| MEDLINE | ID: mdl-16925796
13.
A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO.
Br J Haematol
; 135(5): 603-33, 2006 Dec.
Article
in English
| MEDLINE | ID: mdl-17107346
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