-
1
-
-
84908503345
-
Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey
-
Gresele P, Harrison P, Bury L, Falcinelli E, Gachet C, Hayward C, Kenny D, Mezzano D, Mumford AD, Nugent D, Nurden AT, Orsini S, Cattaneo M. Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey. J Thromb Haemost 2014; 12: 1562-9.
-
(2014)
J Thromb Haemost
, vol.12
, pp. 1562-1569
-
-
Gresele, P.1
Harrison, P.2
Bury, L.3
Falcinelli, E.4
Gachet, C.5
Hayward, C.6
Kenny, D.7
Mezzano, D.8
Mumford, A.D.9
Nugent, D.10
Nurden, A.T.11
Orsini, S.12
Cattaneo, M.13
-
2
-
-
77955042267
-
Inherited disorders of platelet function and challenges to diagnosis of mucocutaneous bleeding
-
Israels SJ, El-Ekiaby M, Quiroga T, Mezzano D. Inherited disorders of platelet function and challenges to diagnosis of mucocutaneous bleeding. Haemophilia 2010; 16: 152-9.
-
(2010)
Haemophilia
, vol.16
, pp. 152-159
-
-
Israels, S.J.1
El-Ekiaby, M.2
Quiroga, T.3
Mezzano, D.4
-
3
-
-
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
-
4
-
-
33646129692
-
Congenital platelet disorders: overview of their mechanisms, diagnostic evaluation and treatment
-
Hayward CP, Rao AK, Cattaneo M. Congenital platelet disorders: overview of their mechanisms, diagnostic evaluation and treatment. Haemophilia 2006; 12: 128-36.
-
(2006)
Haemophilia
, vol.12
, pp. 128-136
-
-
Hayward, C.P.1
Rao, A.K.2
Cattaneo, M.3
-
5
-
-
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
-
6
-
-
0242495669
-
In vitro assays for evaluating platelet function
-
In: Gresele P, Page CP, Fuster V, Vermylen J, eds. Cambridge, UK: Cambridge University Press
-
Thiagarajan P, Wu KK. In vitro assays for evaluating platelet function. In: Gresele P, Page CP, Fuster V, Vermylen J, eds. Platelets in Thrombotic and Non-thrombotic Disorders. Pathophysiology, Pharmacology and Therapeutics. Cambridge, UK: Cambridge University Press, 2002: 459-70.
-
(2002)
Platelets in Thrombotic and Non-thrombotic Disorders. Pathophysiology, Pharmacology and Therapeutics
, pp. 459-470
-
-
Thiagarajan, P.1
Wu, K.K.2
-
7
-
-
84933513562
-
Laboratory investigation of platelets
-
In: Gresele P, Fuster V, Lopez JA, Page CP, Vermylen J, eds. Cambridge, UK: Cambridge University Press
-
Shantsila E, Watson T, Lip GYH. Laboratory investigation of platelets. In: Gresele P, Fuster V, Lopez JA, Page CP, Vermylen J, eds. Platelets in Hematologic and Cardiovascular Disorders: A Clinical Handbook. Cambridge, UK: Cambridge University Press, 2008: 124-46.
-
(2008)
Platelets in Hematologic and Cardiovascular Disorders: A Clinical Handbook
, pp. 124-146
-
-
Shantsila, E.1
Watson, T.2
Lip, G.Y.H.3
-
8
-
-
33645557848
-
Platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet function
-
Platelet Physiology Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
-
Hayward CP, Harrison P, Cattaneo M, Ortel TL, Rao AK, Platelet Physiology Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet function. J Thromb Haemost 2006; 4: 312-9.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 312-319
-
-
Hayward, C.P.1
Harrison, P.2
Cattaneo, M.3
Ortel, T.L.4
Rao, A.K.5
-
9
-
-
77955893209
-
Testing for inherited platelet defects in clinical laboratories in Germany, Austria and Switzerland. Results of a survey carried out by the Permanent Paediatric Group of the German Thrombosis and Hemostasis Research Society (GTH)
-
Streif W, Oliveri M, Weickardt S, Eberl W, Knoefler R, Thromkid Study Group of GTH. Testing for inherited platelet defects in clinical laboratories in Germany, Austria and Switzerland. Results of a survey carried out by the Permanent Paediatric Group of the German Thrombosis and Hemostasis Research Society (GTH). Platelets 2010; 21: 470-8.
-
(2010)
Platelets
, vol.21
, pp. 470-478
-
-
Streif, W.1
Oliveri, M.2
Weickardt, S.3
Eberl, W.4
Knoefler, R.5
-
10
-
-
84859947727
-
Approaches to investigating common bleeding disorders: an evaluation of North American coagulation laboratory practices
-
Hayward CP, Moffat KA, Plumhoff E, Van Cott EM. Approaches to investigating common bleeding disorders: an evaluation of North American coagulation laboratory practices. Am J Hematol 2012; 87: S45-50.
-
(2012)
Am J Hematol
, vol.87
, pp. S45-S50
-
-
Hayward, C.P.1
Moffat, K.A.2
Plumhoff, E.3
Van Cott, E.M.4
-
11
-
-
15344344771
-
Variability in clinical laboratory practice in testing for disorders of platelet function: results of two surveys of the North American Specialized Coagulation Laboratory Association
-
Moffat KA, Ledford-Kraemer MR, Nichols WL, Hayward CP, North American Specialized Coagulation Laboratory Association. Variability in clinical laboratory practice in testing for disorders of platelet function: results of two surveys of the North American Specialized Coagulation Laboratory Association. Thromb Haemost 2005; 93: 549-53.
-
(2005)
Thromb Haemost
, vol.93
, pp. 549-553
-
-
Moffat, K.A.1
Ledford-Kraemer, M.R.2
Nichols, W.L.3
Hayward, C.P.4
-
12
-
-
33750546250
-
A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO
-
Bolton-Maggs PH, Chalmers EA, Collins PW, Harrison P, Kitchen S, Liesner RJ, Minford A, Mumford AD, Parapia LA, Perry DJ, Watson SP, Wilde JT, Williams MD, UKHCDO. A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO. Br J Haematol 2006; 135: 603-33.
-
(2006)
Br J Haematol
, vol.135
, pp. 603-633
-
-
Bolton-Maggs, P.H.1
Chalmers, E.A.2
Collins, P.W.3
Harrison, P.4
Kitchen, S.5
Liesner, R.J.6
Minford, A.7
Mumford, A.D.8
Parapia, L.A.9
Perry, D.J.10
Watson, S.P.11
Wilde, J.T.12
Williams, M.D.13
-
13
-
-
78649643870
-
Development of North American consensus guidelines for medical laboratories that perform and interpret platelet function testing using light transmission aggregometry
-
Hayward CP, Moffat KA, Raby A, Israels S, Plumhoff E, Flynn G, Zehnder JL. Development of North American consensus guidelines for medical laboratories that perform and interpret platelet function testing using light transmission aggregometry. Am J Clin Pathol 2010; 134: 955-63.
-
(2010)
Am J Clin Pathol
, vol.134
, pp. 955-963
-
-
Hayward, C.P.1
Moffat, K.A.2
Raby, A.3
Israels, S.4
Plumhoff, E.5
Flynn, G.6
Zehnder, J.L.7
-
14
-
-
80052574167
-
Guidelines for the laboratory investigation of heritable disorders of platelet function
-
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
-
15
-
-
69249209986
-
The level of laboratory testing required for diagnosis or exclusion of a platelet function disorder using platelet aggregation and secretion assays
-
Mezzano D, Quiroga T, Pereira J. The level of laboratory testing required for diagnosis or exclusion of a platelet function disorder using platelet aggregation and secretion assays. Semin Thromb Hemost 2009; 35: 242-54.
-
(2009)
Semin Thromb Hemost
, vol.35
, pp. 242-254
-
-
Mezzano, D.1
Quiroga, T.2
Pereira, J.3
-
16
-
-
77957851698
-
Diagnosis and management of inherited platelet disorders
-
Kirchmaier CM, Pillitteri D. Diagnosis and management of inherited platelet disorders. Transfus Med Hemother 2010; 37: 237-46.
-
(2010)
Transfus Med Hemother
, vol.37
, pp. 237-246
-
-
Kirchmaier, C.M.1
Pillitteri, D.2
-
17
-
-
77957843636
-
Current strategies in diagnosis of inherited storage pool defects
-
Sandrock K, Zieger B. Current strategies in diagnosis of inherited storage pool defects. Transfus Med Hemother 2010; 37: 248-58.
-
(2010)
Transfus Med Hemother
, vol.37
, pp. 248-258
-
-
Sandrock, K.1
Zieger, B.2
-
18
-
-
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
-
19
-
-
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
-
20
-
-
84903949963
-
Inherited platelet disorders including Glanzmann thrombasthenia and Bernard-Soulier syndrome
-
Diz-Kucukkaya R. Inherited platelet disorders including Glanzmann thrombasthenia and Bernard-Soulier syndrome. Hematology Am Soc Hematol Educ Program 2013; 2013: 268-75.
-
(2013)
Hematology Am Soc Hematol Educ Program
, vol.2013
, pp. 268-275
-
-
Diz-Kucukkaya, R.1
-
21
-
-
84872275085
-
Inherited thrombocytopenias: an approach to diagnosis and management
-
Geddis AE. Inherited thrombocytopenias: an approach to diagnosis and management. Int J Lab Hematol 2013; 35: 14-25.
-
(2013)
Int J Lab Hematol
, vol.35
, pp. 14-25
-
-
Geddis, A.E.1
-
22
-
-
84892404997
-
Genetic sequence analysis of inherited bleeding diseases
-
Peyvandi F, Kunicki T, Lillicrap D. Genetic sequence analysis of inherited bleeding diseases. Blood 2013; 122: 3423-31.
-
(2013)
Blood
, vol.122
, pp. 3423-3431
-
-
Peyvandi, F.1
Kunicki, T.2
Lillicrap, D.3
-
23
-
-
84903976193
-
Laboratory diagnostics of inherited platelet disorders
-
Carubbi C, Masselli E, Nouvenne A, Russo D, Galli D, Mirandola P, Gobbi G, Vitale M. Laboratory diagnostics of inherited platelet disorders. Clin Chem Lab Med 2014; 52: 1091-106.
-
(2014)
Clin Chem Lab Med
, vol.52
, pp. 1091-1106
-
-
Carubbi, C.1
Masselli, E.2
Nouvenne, A.3
Russo, D.4
Galli, D.5
Mirandola, P.6
Gobbi, G.7
Vitale, M.8
-
24
-
-
79961094789
-
Inherited platelet disorders: a clinical approach to diagnosis and management
-
Cox K, Price V, Kahr WH. Inherited platelet disorders: a clinical approach to diagnosis and management. Expert Rev Hematol 2011; 4: 455-72.
-
(2011)
Expert Rev Hematol
, vol.4
, pp. 455-472
-
-
Cox, K.1
Price, V.2
Kahr, W.H.3
-
25
-
-
84898057733
-
What is the role of genetic testing in the investigation of patients with suspected platelet function disorders?
-
Daly ME, Leo VC, Lowe GC, Watson SP, Morgan NV. What is the role of genetic testing in the investigation of patients with suspected platelet function disorders? Br J Haematol 2014; 165: 193-203.
-
(2014)
Br J Haematol
, vol.165
, pp. 193-203
-
-
Daly, M.E.1
Leo, V.C.2
Lowe, G.C.3
Watson, S.P.4
Morgan, N.V.5
-
26
-
-
77956493323
-
ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders
-
Rodeghiero F, Tosetto A, Abshire T, Arnold DM, Coller B, James P, Neunert C, Lillicrap D, ISTH/SSC joint VWF, 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
-
27
-
-
34250696130
-
How to estimate bleeding risk in mild bleeding disorders
-
Rodeghiero F, Tosetto A, Castaman G. How to estimate bleeding risk in mild bleeding disorders. J Thromb Haemost 2007; 5: 157-66.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 157-166
-
-
Rodeghiero, F.1
Tosetto, A.2
Castaman, G.3
-
28
-
-
84883786964
-
Utility of the ISTH bleeding assessment tool in predicting platelet defects in participants with suspected inherited platelet function disorders
-
Lowe GC, Lordkipanidzé M, Watson SP, 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
-
29
-
-
84868541229
-
Drugs that affect platelet function
-
Scharf RE. Drugs that affect platelet function. Semin Thromb Hemost 2012; 38: 865-83.
-
(2012)
Semin Thromb Hemost
, vol.38
, pp. 865-883
-
-
Scharf, R.E.1
-
31
-
-
84863446168
-
Prospective evaluation of a pediatric bleeding questionnaire and the ISTH bleeding assessment tool in children and parents in routine clinical practice
-
Bidlingmaier C, Grote V, Budde U, Olivieri M, Kurnik K. Prospective evaluation of a pediatric bleeding questionnaire and the ISTH bleeding assessment tool in children and parents in routine clinical practice. J Thromb Haemost 2012; 10: 1335-41.
-
(2012)
J Thromb Haemost
, vol.10
, pp. 1335-1341
-
-
Bidlingmaier, C.1
Grote, V.2
Budde, U.3
Olivieri, M.4
Kurnik, K.5
-
33
-
-
36349021373
-
Usefulness of PFA-100 testing in the diagnostic screening of patients with suspected abnormalities of hemostasis: comparison with the bleeding time
-
Podda GM, Bucciarelli P, Lussana F, Lecchi A, Cattaneo M. Usefulness of PFA-100 testing in the diagnostic screening of patients with suspected abnormalities of hemostasis: comparison with the bleeding time. J Thromb Haemost 2007; 5: 2393-8.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 2393-2398
-
-
Podda, G.M.1
Bucciarelli, P.2
Lussana, F.3
Lecchi, A.4
Cattaneo, M.5
-
34
-
-
84892373418
-
Usefulness of the INNOVANCE PFA P2Y test cartridge for the detection of patients with congenital defects of the platelet P2Y12 receptor for adenosine diphosphate
-
Scavone M, Germanovich K, Femia EA, Cattaneo M. Usefulness of the INNOVANCE PFA P2Y test cartridge for the detection of patients with congenital defects of the platelet P2Y12 receptor for adenosine diphosphate. Thromb Res 2014; 133: 254-6.
-
(2014)
Thromb Res
, vol.133
, pp. 254-256
-
-
Scavone, M.1
Germanovich, K.2
Femia, E.A.3
Cattaneo, M.4
-
35
-
-
34247354643
-
Spectrum of Von Willebrand disease and inherited platelet function disorders amongst Indian bleeders
-
Gupta PK, Charan VD, Saxena R. Spectrum of Von Willebrand disease and inherited platelet function disorders amongst Indian bleeders. Ann Hematol 2007; 86: 403-7.
-
(2007)
Ann Hematol
, vol.86
, pp. 403-407
-
-
Gupta, P.K.1
Charan, V.D.2
Saxena, R.3
-
36
-
-
0043260603
-
A simple method for measuring clot retraction
-
MacFarlane RG. A simple method for measuring clot retraction. Lancet 1939; 233: 1199-201.
-
(1939)
Lancet
, vol.233
, pp. 1199-1201
-
-
MacFarlane, R.G.1
-
37
-
-
0028832243
-
Studies on the haemostatic defect in a complicated syndrome. An inverse Scott syndrome platelet membrane abnormality?
-
Stormorken H, Holmsen H, Sund R, Sakariassen KS, Hovig T, Jellum E, Solum O. Studies on the haemostatic defect in a complicated syndrome. An inverse Scott syndrome platelet membrane abnormality? Thromb Haemost 1995; 74: 1244-51.
-
(1995)
Thromb Haemost
, vol.74
, pp. 1244-1251
-
-
Stormorken, H.1
Holmsen, H.2
Sund, R.3
Sakariassen, K.S.4
Hovig, T.5
Jellum, E.6
Solum, O.7
-
38
-
-
45749138315
-
Inherited human cPLA(2alpha) deficiency is associated with impaired eicosanoid biosynthesis, small intestinal ulceration, and platelet dysfunction
-
Adler DH, Cogan JD, Phillips JA III, Schnetz-Boutaud N, Milne GL, Iverson T, Stein JA, Brenner DA, Morrow JD, Boutaud O, Oates JA. Inherited human cPLA(2alpha) deficiency is associated with impaired eicosanoid biosynthesis, small intestinal ulceration, and platelet dysfunction. J Clin Invest 2008; 118: 2121-31.
-
(2008)
J Clin Invest
, vol.118
, pp. 2121-2131
-
-
Adler, D.H.1
Cogan, J.D.2
Phillips, J.A.3
Schnetz-Boutaud, N.4
Milne, G.L.5
Iverson, T.6
Stein, J.A.7
Brenner, D.A.8
Morrow, J.D.9
Boutaud, O.10
Oates, J.A.11
-
39
-
-
0034943053
-
Characterization of a partial prostaglandin endoperoxide H synthase-1 deficiency in a patient with a bleeding disorder
-
Dubé JN, Drouin J, Aminian M, Plant MH, Laneuville O. Characterization of a partial prostaglandin endoperoxide H synthase-1 deficiency in a patient with a bleeding disorder. Br J Haematol 2001; 113: 878-85.
-
(2001)
Br J Haematol
, vol.113
, pp. 878-885
-
-
Dubé, J.N.1
Drouin, J.2
Aminian, M.3
Plant, M.H.4
Laneuville, O.5
-
40
-
-
0019440982
-
Familial bleeding tendency with partial platelet thromboxane synthetase deficiency: reorientation of cyclic endoperoxide metabolism
-
Defreyn G, Machin SJ, Carreras LO, Dauden MV, Chamone DA, Vermylen J. Familial bleeding tendency with partial platelet thromboxane synthetase deficiency: reorientation of cyclic endoperoxide metabolism. Br J Haematol 1981; 49: 29-41.
-
(1981)
Br J Haematol
, vol.49
, pp. 29-41
-
-
Defreyn, G.1
Machin, S.J.2
Carreras, L.O.3
Dauden, M.V.4
Chamone, D.A.5
Vermylen, J.6
-
42
-
-
46749112199
-
An evaluation of methods for determining reference intervals for light transmission platelet aggregation tests on samples with normal or reduced platelet counts
-
Hayward CP, Moffat KA, Pai M, Liu Y, Seecharan J, McKay H, Webert KE, Cook RJ, Heddle NM. An evaluation of methods for determining reference intervals for light transmission platelet aggregation tests on samples with normal or reduced platelet counts. Thromb Haemost 2008; 100: 134-45.
-
(2008)
Thromb Haemost
, vol.100
, pp. 134-145
-
-
Hayward, C.P.1
Moffat, K.A.2
Pai, M.3
Liu, Y.4
Seecharan, J.5
McKay, H.6
Webert, K.E.7
Cook, R.J.8
Heddle, N.M.9
-
43
-
-
84905455420
-
A loss of function screen of identified genome-wide association study Loci reveals new genes controlling hematopoiesis
-
Bielczyk-Maczyńska E, Serbanovic-Canic J, Ferreira L, Soranzo N, Stemple DL, Ouwehand WH, Cvejic A. A loss of function screen of identified genome-wide association study Loci reveals new genes controlling hematopoiesis. PLoS Genet 2014; 10: e1004450.
-
(2014)
PLoS Genet
, vol.10
, pp. e1004450
-
-
Bielczyk-Maczyńska, E.1
Serbanovic-Canic, J.2
Ferreira, L.3
Soranzo, N.4
Stemple, D.L.5
Ouwehand, W.H.6
Cvejic, A.7
-
44
-
-
77949281858
-
Phenotypic approaches to gene mapping in platelet function disorders - identification of new variant of P2Y12, TxA2 and GPVI receptors
-
Watson S, Daly M, Dawood B, Gissen P, Makris M, Mundell S, Wilde J, Mumford A. Phenotypic approaches to gene mapping in platelet function disorders - identification of new variant of P2Y12, TxA2 and GPVI receptors. Hamostaseologie 2010; 30: 29-38.
-
(2010)
Hamostaseologie
, vol.30
, pp. 29-38
-
-
Watson, S.1
Daly, M.2
Dawood, B.3
Gissen, P.4
Makris, M.5
Mundell, S.6
Wilde, J.7
Mumford, A.8
-
45
-
-
0038777336
-
Inherited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle Piastrine
-
Balduini CL, Cattaneo M, Fabris F, Gresele P, Iolascon A, Pulcinelli FM, Savoia A, Italian Gruppo di Studio delle Piastrine. Inherited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle Piastrine. Haematologica 2003; 88: 582-92.
-
(2003)
Haematologica
, vol.88
, pp. 582-592
-
-
Balduini, C.L.1
Cattaneo, M.2
Fabris, F.3
Gresele, P.4
Iolascon, A.5
Pulcinelli, F.M.6
Savoia, A.7
-
46
-
-
6344281238
-
Application of a diagnostic algorithm for inherited thrombocytopenias to 46 consecutive patients
-
Noris P, Pecci A, Di Bari F, Di Stazio MT, Di Pumpo M, Ceresa IF, Arezzi N, Ambaglio C, Savoia A, Balduini CL. Application of a diagnostic algorithm for inherited thrombocytopenias to 46 consecutive patients. Haematologica 2004; 89: 1219-25.
-
(2004)
Haematologica
, vol.89
, pp. 1219-1225
-
-
Noris, P.1
Pecci, A.2
Di Bari, F.3
Di Stazio, M.T.4
Di Pumpo, M.5
Ceresa, I.F.6
Arezzi, N.7
Ambaglio, C.8
Savoia, A.9
Balduini, C.L.10
-
47
-
-
84865222824
-
International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country
-
Glembotsky AC, Marta RF, Pecci A, De Rocco D, Gnan C, Espasandin YR, Goette NP, Negro F, Noris P, Savoia A, Balduini CL, Molinas FC, Heller PG. International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country. J Thromb Haemost 2012; 10: 1653-61.
-
(2012)
J Thromb Haemost
, vol.10
, pp. 1653-1661
-
-
Glembotsky, A.C.1
Marta, R.F.2
Pecci, A.3
De Rocco, D.4
Gnan, C.5
Espasandin, Y.R.6
Goette, N.P.7
Negro, F.8
Noris, P.9
Savoia, A.10
Balduini, C.L.11
Molinas, F.C.12
Heller, P.G.13
|