-
1
-
-
84880578527
-
Genotyping and phenotyping of platelet function disorders
-
on behalf of the GAPP consortium.
-
Watson SP, Lowe GC, Lordkipanidzé M, Morgan NV; on behalf of the GAPP consortium. Genotyping and phenotyping of platelet function disorders. J Thromb Haemost 2013; 11 (Suppl. 1): 351-63.
-
(2013)
J Thromb Haemost
, vol.11
, Issue.SUPPL. 1
, pp. 351-363
-
-
Watson, S.P.1
Lowe, G.C.2
Lordkipanidzé, M.3
Morgan, N.V.4
-
2
-
-
84876497746
-
Is my patient a bleeder? A diagnostic framework for mild bleeding disorders
-
Quiroga T, Mezzano D. Is my patient a bleeder? A diagnostic framework for mild bleeding disorders. Hematology Am Soc Hematol Educ Program 2012; 2012: 466-74.
-
(2012)
Hematology Am Soc Hematol Educ Program
, vol.2012
, pp. 466-474
-
-
Quiroga, T.1
Mezzano, D.2
-
3
-
-
0021351638
-
Platelet function testing: an improved approach utilizing lumi-aggregation and an interactive computer system
-
Miller JL. Platelet function testing: an improved approach utilizing lumi-aggregation and an interactive computer system. Am J Clin Pathol 1984; 81: 471-6.
-
(1984)
Am J Clin Pathol
, vol.81
, pp. 471-476
-
-
Miller, J.L.1
-
4
-
-
0023608663
-
Patients with a prolonged bleeding time and normal aggregation tests may have storage pool deficiency: studies on one hundred six patients
-
Nieuwenhuis HK, Akkerman JW, Sixma JJ. Patients with a prolonged bleeding time and normal aggregation tests may have storage pool deficiency: studies on one hundred six patients. Blood 1987; 70: 620-3.
-
(1987)
Blood
, vol.70
, pp. 620-623
-
-
Nieuwenhuis, H.K.1
Akkerman, J.W.2
Sixma, J.J.3
-
5
-
-
84871027512
-
Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel
-
Dawood BB, Lowe GC, Lordkipanidzé M, Bem D, Daly ME, Makris M, Mumford A, Wilde JT, Watson SP. Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel. Blood 2012; 120: 5041-9.
-
(2012)
Blood
, vol.120
, pp. 5041-5049
-
-
Dawood, B.B.1
Lowe, G.C.2
Lordkipanidzé, M.3
Bem, D.4
Daly, M.E.5
Makris, M.6
Mumford, A.7
Wilde, J.T.8
Watson, S.P.9
-
6
-
-
34247606049
-
High prevalence of bleeders of unknown cause among patients with inherited mucocutaneous bleeding. A prospective study of 280 patients and 299 controls
-
Quiroga T, Goycoolea M, Panes O, Aranda E, Martínez C, Belmont S, Muñoz B, Zúñiga P, Pereira J, Mezzano D. High prevalence of bleeders of unknown cause among patients with inherited mucocutaneous bleeding. A prospective study of 280 patients and 299 controls. Haematologica 2007; 92: 357-65.
-
(2007)
Haematologica
, vol.92
, pp. 357-365
-
-
Quiroga, T.1
Goycoolea, M.2
Panes, O.3
Aranda, E.4
Martínez, C.5
Belmont, S.6
Muñoz, B.7
Zúñiga, P.8
Pereira, J.9
Mezzano, D.10
-
7
-
-
80052574167
-
Guidelines for the laboratory investigation of heritable disorders of platelet function
-
British Committee for Standards in Haematology.
-
Harrison P, Mackie I, Mumford A, Briggs C, Liesner R, Winter M, Machin S; British Committee for Standards in Haematology. Guidelines for the laboratory investigation of heritable disorders of platelet function. Br J Haematol 2011; 155: 30-44.
-
(2011)
Br J Haematol
, vol.155
, pp. 30-44
-
-
Harrison, P.1
Mackie, I.2
Mumford, A.3
Briggs, C.4
Liesner, R.5
Winter, M.6
Machin, S.7
-
8
-
-
85043081840
-
-
WO 2008107724 A2 University of Nottingham, patent application number PCT/GB2008/050169, stabilisation of biological cell markers.
-
Fox SC, May JA, Heptinstall S. WO 2008107724 A2 University of Nottingham, patent application number PCT/GB2008/050169, stabilisation of biological cell markers. 2008.
-
(2008)
-
-
Fox, S.C.1
May, J.A.2
Heptinstall, S.3
-
9
-
-
77956493323
-
ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders
-
ISTH/SSC joint VWF and Perinatal/Pediatric Hemostasis Subcommittees Working Group.
-
Rodeghiero F, Tosetto A, Abshire T, Arnold DM, Coller B, James P, Neunert C, Lillicrap D; ISTH/SSC joint VWF and Perinatal/Pediatric Hemostasis Subcommittees Working Group. ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders. J Thromb Haemost 2010; 8: 2063-5.
-
(2010)
J Thromb Haemost
, vol.8
, pp. 2063-2065
-
-
Rodeghiero, F.1
Tosetto, A.2
Abshire, T.3
Arnold, D.M.4
Coller, B.5
James, P.6
Neunert, C.7
Lillicrap, D.8
-
10
-
-
84883786964
-
Utility of the ISTH Bleeding Assessment Tool in predicting platelet defects in participants with suspected inherited platelet function disorders
-
on behalf of the UK GAPP study group.
-
Lowe GC, Lordkipanidzé M, Watson SP; on behalf of the UK GAPP study group. Utility of the ISTH Bleeding Assessment Tool in predicting platelet defects in participants with suspected inherited platelet function disorders. J Thromb Haemost 2013; 11: 1663-8.
-
(2013)
J Thromb Haemost
, vol.11
, pp. 1663-1668
-
-
Lowe, G.C.1
Lordkipanidzé, M.2
Watson, S.P.3
-
11
-
-
67651154318
-
Measurement of platelet P-selectin for remote testing of platelet function during treatment with clopidogrel and/or aspirin
-
Fox SC, May JA, Shah A, Neubert U, Heptinstall S. Measurement of platelet P-selectin for remote testing of platelet function during treatment with clopidogrel and/or aspirin. Platelets 2009; 20: 250-9.
-
(2009)
Platelets
, vol.20
, pp. 250-259
-
-
Fox, S.C.1
May, J.A.2
Shah, A.3
Neubert, U.4
Heptinstall, S.5
-
12
-
-
84875941591
-
Microsatellite markers as a rapid approach for autozygosity mapping in Hermansky-Pudlak syndrome: identification of the second HPS7 mutation in a patient presenting late in life
-
UK GAPP collaborative.
-
Lowe GC, Sánchez Guiu I, Chapman O, Rivera J, Lordkipanidzé M, Dovlatova N, Wilde J, Watson SP, Morgan NV; UK GAPP collaborative. Microsatellite markers as a rapid approach for autozygosity mapping in Hermansky-Pudlak syndrome: identification of the second HPS7 mutation in a patient presenting late in life. Thromb Haemost 2013; 109: 766-8.
-
(2013)
Thromb Haemost
, vol.109
, pp. 766-768
-
-
Lowe, G.C.1
Sánchez Guiu, I.2
Chapman, O.3
Rivera, J.4
Lordkipanidzé, M.5
Dovlatova, N.6
Wilde, J.7
Watson, S.P.8
Morgan, N.V.9
-
13
-
-
0033007616
-
Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the beta 3A subunit of the AP-3 adaptor
-
Dell'Angelica EC, Shotelersuk V, Aguilar RC, Gahl WA, Bonifacino JS. Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the beta 3A subunit of the AP-3 adaptor. Mol Cell 1999; 3: 11-21.
-
(1999)
Mol Cell
, vol.3
, pp. 11-21
-
-
Dell'Angelica, E.C.1
Shotelersuk, V.2
Aguilar, R.C.3
Gahl, W.A.4
Bonifacino, J.S.5
-
14
-
-
70249101426
-
Results of a worldwide survey on the assessment of platelet function by light transmission aggregometry: a report from the platelet physiology subcommittee of the SSC of the ISTH
-
Cattaneo M, Hayward CP, Moffat KA, Pugliano MT, Liu Y, Michelson AD. Results of a worldwide survey on the assessment of platelet function by light transmission aggregometry: a report from the platelet physiology subcommittee of the SSC of the ISTH. J Thromb Haemost 2009; 7: 1029.
-
(2009)
J Thromb Haemost
, vol.7
, pp. 1029
-
-
Cattaneo, M.1
Hayward, C.P.2
Moffat, K.A.3
Pugliano, M.T.4
Liu, Y.5
Michelson, A.D.6
-
15
-
-
84883825698
-
Recommendations for the standardization of light transmission aggregometry: a consensus of the working party from the platelet physiology subcommittee of SSC/ISTH
-
Cattaneo M, Cerletti C, Harrison P, Hayward CP, Kenny D, Nugent D, Nurden P, Rao AK, Schmaier AH, Watson SP, Lussana F, Pugliano MT, Michelson AD. Recommendations for the standardization of light transmission aggregometry: a consensus of the working party from the platelet physiology subcommittee of SSC/ISTH. J Thromb Haemost 2013; 11: 1183-9.
-
(2013)
J Thromb Haemost
, vol.11
, pp. 1183-1189
-
-
Cattaneo, M.1
Cerletti, C.2
Harrison, P.3
Hayward, C.P.4
Kenny, D.5
Nugent, D.6
Nurden, P.7
Rao, A.K.8
Schmaier, A.H.9
Watson, S.P.10
Lussana, F.11
Pugliano, M.T.12
Michelson, A.D.13
|