-
1
-
-
0027458101
-
Prevalence of von Willebrand disease in children: A multiethnic study
-
DOI 10.1016/S0022-3476(05)80384-1
-
Werner E J., Broxson E H., Tucker E L., Giroux D S., Shults J, Abshire T C. Prevalence of von Willebrand disease in children: a multiethnic study. J Pediatr 1993 123 6 893-898 (Pubitemid 23353251)
-
(1993)
Journal of Pediatrics
, vol.123
, Issue.6
, pp. 893-898
-
-
Werner, E.J.1
Broxson, E.H.2
Tucker, E.L.3
Giroux, D.S.4
Shults, J.5
Abshire, T.C.6
-
2
-
-
73049112574
-
The prevalence of symptomatic von Willebrand disease in primary care practice
-
Bowman M, Hopman W M., Rapson D, Lillicrap D, James P. The prevalence of symptomatic von Willebrand disease in primary care practice. J Thromb Haemost 2010 8 1 213-216
-
(2010)
J Thromb Haemost
, vol.8
, Issue.1
, pp. 213-216
-
-
Bowman, M.1
Hopman, W.M.2
Rapson, D.3
Lillicrap, D.4
James, P.5
-
3
-
-
77953283530
-
A prospective evaluation of the prevalence of symptomatic von Willebrand disease (VWD) in a pediatric primary care population
-
Bowman M, Hopman W M., Rapson D, Lillicrap D, Silva M, James P. A prospective evaluation of the prevalence of symptomatic von Willebrand disease (VWD) in a pediatric primary care population. Pediatr Blood Cancer 2010 55 1 171-173
-
(2010)
Pediatr Blood Cancer
, vol.55
, Issue.1
, pp. 171-173
-
-
Bowman, M.1
Hopman, W.M.2
Rapson, D.3
Lillicrap, D.4
Silva, M.5
James, P.6
-
4
-
-
44249092303
-
Rare bleeding disorders
-
DOI 10.1111/j.1365-2516.2008.01751.x, State of the Art.XXVIII International Congress of the World Federation of Hemophilia
-
Peyvandi F, Cattaneo M, Inbal A, De Moerloose P, Spreafico M. Rare bleeding disorders. Haemophilia 2008 14 Suppl 3 202-210 (Pubitemid 351722403)
-
(2008)
Haemophilia
, vol.14
, Issue.SUPPL. 3
, pp. 202-210
-
-
Peyvandi, F.1
Cattaneo, M.2
Inbal, A.3
De Moerloose, P.4
Spreafico, M.5
-
5
-
-
41149168746
-
Inherited traits affecting platelet function
-
Salles I I., Feys H B., Iserbyt B F., De Meyer S F., Vanhoorelbeke K, Deckmyn H. Inherited traits affecting platelet function. Blood Rev 2008 22 3 155-172
-
(2008)
Blood Rev
, vol.22
, Issue.3
, pp. 155-172
-
-
Salles, I.I.1
Feys, H.B.2
Iserbyt, B.F.3
De Meyer, S.F.4
Vanhoorelbeke, K.5
Deckmyn, H.6
-
6
-
-
38949096839
-
Congenital disorders associated with platelet dysfunctions
-
DOI 10.1160/TH07-09-0568
-
Nurden P, Nurden A T. Congenital disorders associated with platelet dysfunctions. Thromb Haemost 2008 99 2 253-263 (Pubitemid 351230953)
-
(2008)
Thrombosis and Haemostasis
, vol.99
, Issue.2
, pp. 253-263
-
-
Nurden, P.1
Nurden, A.T.2
-
7
-
-
33646129692
-
Congenital platelet disorders: Overview of their mechanisms, diagnostic evaluation and treatment
-
Suppl 3
-
Hayward C P., Rao A K., Cattaneo M. Congenital platelet disorders: overview of their mechanisms, diagnostic evaluation and treatment. Haemophilia 2006 12 Suppl 3 128-136
-
(2006)
Haemophilia
, vol.12
, pp. 128-136
-
-
Hayward, C.P.1
Rao, A.K.2
Cattaneo, M.3
-
8
-
-
41149114176
-
Childhood Immune Thrombocytopenic Purpura: Diagnosis and Management
-
DOI 10.1016/j.pcl.2008.01.009, PII S0031395508000631
-
Blanchette V S., Bolton-Maggs P. Childhood immune thrombocytopenic purpura: diagnosis and management. Pediatr Clin North Am 2008 55 2 393-420, ix (Pubitemid 351442783)
-
(2008)
Pediatric Clinics of North America
, vol.55
, Issue.2
, pp. 393-420
-
-
Blanchette, V.1
Bolton-Maggs, P.2
-
10
-
-
17144445992
-
Delayed umbilical bleedinga presenting feature for factor XIII deficiency: Clinical features, genetics, and management
-
Anwar R, Minford A, Gallivan L, Trinh C H., Markham A F. Delayed umbilical bleedinga presenting feature for factor XIII deficiency: clinical features, genetics, and management. Pediatrics 2002 109 2 E32
-
(2002)
Pediatrics
, vol.109
, Issue.2
-
-
Anwar, R.1
Minford, A.2
Gallivan, L.3
Trinh, C.H.4
Markham, A.F.5
-
11
-
-
84863330934
-
-
In: Lee C. Berntorp E. Hoots K. eds. Textbook of Hemophilia. 2nd ed West, Sussex, UK Blackwell
-
Carcao M D., Blanchette V S. Work-up of a bleeding child. In: Lee C Berntorp E Hoots K eds. Textbook of Hemophilia. 2nd ed. West, Sussex, UK Blackwell 2010 118-126
-
(2010)
Work-up of A Bleeding Child
, pp. 118-126
-
-
Carcao, M.D.1
Blanchette, V.S.2
-
12
-
-
67849097372
-
Factor XI deficiency in humans
-
Suppl 1
-
Seligsohn U. Factor XI deficiency in humans. J Thromb Haemost 2009 7 Suppl 1 84-87
-
(2009)
J Thromb Haemost
, vol.7
, pp. 84-87
-
-
Seligsohn, U.1
-
14
-
-
0025804299
-
Bleeding/bruising symptomatology in children with and without bleeding disorders
-
Nosek-Cenkowska B, Cheang M S., Pizzi N J., Israels E D., Gerrard J M. Bleeding/bruising symptomatology in children with and without bleeding disorders. Thromb Haemost 1991 65 3 237-241
-
(1991)
Thromb Haemost
, vol.65
, Issue.3
, pp. 237-241
-
-
Nosek-Cenkowska, B.1
Cheang, M.S.2
Pizzi, N.J.3
Israels, E.D.4
Gerrard, J.M.5
-
15
-
-
33646146198
-
Laboratory issues in bleeding disorders
-
Suppl 3
-
Lillicrap D, Nair S C., Srivastava A, Rodeghiero F, Pabinger I, Federici A B. Laboratory issues in bleeding disorders. Haemophilia 2006 12 Suppl 3 68-75
-
(2006)
Haemophilia
, vol.12
, pp. 68-75
-
-
Lillicrap, D.1
Nair, S.C.2
Srivastava, A.3
Rodeghiero, F.4
Pabinger, I.5
Federici, A.B.6
-
16
-
-
44249116406
-
Relevance of quantitative assessment of bleeding in haemorrhagic disorders
-
DOI 10.1111/j.1365-2516.2008.01714.x, State of the Art.XXVIII International Congress of the World Federation of Hemophilia
-
Rodeghiero F, Kadir R A., Tosetto A, James P D. Relevance of quantitative assessment of bleeding in haemorrhagic disorders. Haemophilia 2008 14 Suppl 3 68-75 (Pubitemid 351722386)
-
(2008)
Haemophilia
, vol.14
, Issue.SUPPL. 3
, pp. 68-75
-
-
Rodeghiero, F.1
Kadir, R.A.2
Tosetto, A.3
James, P.D.4
-
17
-
-
29244439008
-
The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: An international, multicenter study
-
DOI 10.1111/j.1538-7836.2005.01663.x
-
Rodeghiero F, Castaman G, Tosetto A et al. The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: an international, multicenter study. J Thromb Haemost 2005 3 12 2619-2626 (Pubitemid 41819788)
-
(2005)
Journal of Thrombosis and Haemostasis
, vol.3
, Issue.12
, pp. 2619-2626
-
-
Rodeghiero, F.1
Castaman, G.2
Tosetto, A.3
Batlle, J.4
Baudo, F.5
Cappelletti, A.6
Casana, P.7
De Bosch, N.8
Eikenboom, J.C.J.9
Federici, A.B.10
Lethagen, S.11
Linari, S.12
Srivastava, A.13
-
18
-
-
33644977050
-
A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: Results from a multicenter European study (MCMDM-1 VWD)
-
Tosetto A, Rodeghiero F, Castaman G et al. A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD). J Thromb Haemost 2006 4 4 766-773
-
(2006)
J Thromb Haemost
, vol.4
, Issue.4
, pp. 766-773
-
-
Tosetto, A.1
Rodeghiero, F.2
Castaman, G.3
-
19
-
-
67949091189
-
Evaluation of the diagnostic utility for von Willebrand disease of a pediatric bleeding questionnaire
-
Bowman M, Riddel J, Rand M L., Tosetto A, Silva M, James P D. Evaluation of the diagnostic utility for von Willebrand disease of a pediatric bleeding questionnaire. J Thromb Haemost 2009 7 8 1418-1421
-
(2009)
J Thromb Haemost
, vol.7
, Issue.8
, pp. 1418-1421
-
-
Bowman, M.1
Riddel, J.2
Rand, M.L.3
Tosetto, A.4
Silva, M.5
James, P.D.6
-
20
-
-
77953800564
-
Quantitation of bleeding symptoms in children with von Willebrand disease: Use of a standardized pediatric bleeding questionnaire
-
Biss T T., Blanchette V S., Clark D S. et al. Quantitation of bleeding symptoms in children with von Willebrand disease: use of a standardized pediatric bleeding questionnaire. J Thromb Haemost 2010 8 5 950-956
-
(2010)
J Thromb Haemost
, vol.8
, Issue.5
, pp. 950-956
-
-
Biss, T.T.1
Blanchette, V.S.2
Clark, D.S.3
-
21
-
-
77954506430
-
Use of a quantitative pediatric bleeding questionnaire to assess mucocutaneous bleeding symptoms in children with a platelet function disorder
-
Biss T T., Blanchette V S., Clark D S., Wakefield C D., James P D., Rand M L. Use of a quantitative pediatric bleeding questionnaire to assess mucocutaneous bleeding symptoms in children with a platelet function disorder. J Thromb Haemost 2010 8 6 1416-1419
-
(2010)
J Thromb Haemost
, vol.8
, Issue.6
, pp. 1416-1419
-
-
Biss, T.T.1
Blanchette, V.S.2
Clark, D.S.3
Wakefield, C.D.4
James, P.D.5
Rand, M.L.6
-
22
-
-
43149083497
-
Bleeding scores in inherited bleeding disorders: Clinical or research tools?
-
DOI 10.1111/j.1365-2516.2007.01648.x
-
Tosetto A, Castaman G, Rodeghiero F. Bleeding scores in inherited bleeding disorders: clinical or research tools? Haemophilia 2008 14 3 415-422 (Pubitemid 351638726)
-
(2008)
Haemophilia
, vol.14
, Issue.3
, pp. 415-422
-
-
Tosetto, A.1
Castaman, G.2
Rodeghiero, F.3
-
24
-
-
0038616078
-
Comparison of PFA-100 and bleeding time testing in pediatric paients with suspected hemorrhagic problems
-
DOI 10.1097/00043426-200306000-00009
-
Cariappa R, Wilhite T R., Parvin C A., Luchtman-Jones L. Comparison of PFA-100 and bleeding time testing in pediatric patients with suspected hemorrhagic problems. J Pediatr Hematol Oncol 2003 25 6 474-479 (Pubitemid 36682753)
-
(2003)
Journal of Pediatric Hematology/Oncology
, vol.25
, Issue.6
, pp. 474-479
-
-
Cariappa, R.1
Wilhite, T.R.2
Parvin, C.A.3
Luchtman-Jones, L.4
-
25
-
-
0033935043
-
Comparison of the O'Brien filter test and the PFA-100 platelet analyzer in the laboratory diagnosis of von Willebrand's disease
-
Schlammadinger A, Kerenyi A, Muszbek L, Boda Z. Comparison of the O'Brien filter test and the PFA-100 platelet analyzer in the laboratory diagnosis of von Willebrand's disease. Thromb Haemost 2000 84 1 88-92 (Pubitemid 30433674)
-
(2000)
Thrombosis and Haemostasis
, vol.84
, Issue.1
, pp. 88-92
-
-
Schlammadinger, A.1
Kerenyi, A.2
Muszbek, L.3
Boda, Z.4
-
26
-
-
0141428992
-
Comparison of PFA-100 testing and bleeding time for detecting platelet hypofunction and von Willebrand disease in clinical practice
-
Posan E, McBane R D., Grill D E., Motsko C L., Nichols W L. Comparison of PFA-100 testing and bleeding time for detecting platelet hypofunction and von Willebrand disease in clinical practice. Thromb Haemost 2003 90 3 483-490 (Pubitemid 37138774)
-
(2003)
Thrombosis and Haemostasis
, vol.90
, Issue.3
, pp. 483-490
-
-
Posan, E.1
McBane II, R.D.2
Grill, D.E.3
Motsko, C.L.4
Nichols, W.L.5
-
27
-
-
13244279572
-
Template bleeding time and PFA-100® have low sensitivity to screen patients with hereditary mucocutaneous hemorrhages: Comparative study in 148 patients
-
DOI 10.1111/j.1538-7836.2004.00693.x
-
Quiroga T, Goycoolea M, Muñoz B et al. Template bleeding time and PFA-100 have low sensitivity to screen patients with hereditary mucocutaneous hemorrhages: comparative study in 148 patients. J Thromb Haemost 2004 2 6 892-898 (Pubitemid 40185736)
-
(2004)
Journal of Thrombosis and Haemostasis
, vol.2
, Issue.6
, pp. 892-898
-
-
Quiroga, T.1
Goycoolea, M.2
Munoz, B.3
Morales, M.4
Aranda, E.5
Panes, O.6
Pereira, J.7
Mezzano, D.8
-
28
-
-
0029011142
-
Description of an in vitro platelet function analyzerPFA-100
-
Suppl 2
-
Kundu S K., Heilmann E J., Sio R, Garcia C, Davidson R M., Ostgaard R A. Description of an in vitro platelet function analyzerPFA-100. Semin Thromb Hemost 1995 21 Suppl 2 106-112
-
(1995)
Semin Thromb Hemost
, vol.21
, pp. 106-112
-
-
Kundu, S.K.1
Heilmann, E.J.2
Sio, R.3
Garcia, C.4
Davidson, R.M.5
Ostgaard, R.A.6
-
29
-
-
0032712889
-
Use of a novel platelet function analyzer (PFA-100(TM)) with high sensitivity to disturbances in von Willebrand factor to screen for von Willebrand's disease and other disorders
-
DOI 10.1002/(SICI)1096-8652(1999 11)62:3<165::AI D-AJH6>3.0.CO;2-C
-
Favaloro E J., Facey D, Henniker A. Use of a novel platelet function analyzer (PFA-100) with high sensitivity to disturbances in von Willebrand factor to screen for von Willebrand's disease and other disorders. Am J Hematol 1999 62 3 165-174 (Pubitemid 29521764)
-
(1999)
American Journal of Hematology
, vol.62
, Issue.3
, pp. 165-174
-
-
Favaloro, E.J.1
Facey, D.2
Henniker, A.3
-
30
-
-
0032959927
-
Can the Platelet Function Analyzer (PFA(TM))-100 test substitute for the template bleeding time in routine clinical practice?
-
Francis J, Francis D, Larson L, Helms E, Garcia M. Can the Platelet Function Analyzer (PFA)-100 test substitute for the template bleeding time in routine clinical practice? Platelets 1999 10 2-3 132-136 (Pubitemid 29182281)
-
(1999)
Platelets
, vol.10
, Issue.2-3
, pp. 132-136
-
-
Francis, J.1
Francis, D.2
Larson, L.3
Helms, E.4
Garcia, M.5
-
31
-
-
7144227947
-
The Platelet Function Analyzer (PFA-100®): A novel in-vitro system for evaluation of primary haemostasis in children
-
DOI 10.1046/j.1365-2141.1998.00656.x
-
Carcao M D., Blanchette V S., Dean J A. et al. The Platelet Function Analyzer (PFA-100): a novel in-vitro system for evaluation of primary haemostasis in children. Br J Haematol 1998 101 1 70-73 (Pubitemid 28197777)
-
(1998)
British Journal of Haematology
, vol.101
, Issue.1
, pp. 70-73
-
-
Carcao, M.D.1
Blanchette, V.S.2
Dean, J.A.3
He, L.4
Kern, M.A.5
Stain, A.M.6
Sparling, C.R.7
Stephens, D.8
Ryan, G.9
Freedman, J.10
Rand, M.L.11
-
32
-
-
34249778101
-
Diagnostic performance of the platelet function analyzer (PFA-100®) for the detection of disorders of primary haemostasis in patients with a bleeding history - A systematic review and meta-analysis
-
DOI 10.1080/09537100601100366, PII 779128096
-
Karger R, Donner-Banzhoff N, Müller H H., Kretschmer V, Hunink M. Diagnostic performance of the platelet function analyzer (PFA-100) for the detection of disorders of primary haemostasis in patients with a bleeding history-a systematic review and meta-analysis. Platelets 2007 18 4 249-260 (Pubitemid 46854816)
-
(2007)
Platelets
, vol.18
, Issue.4
, pp. 249-260
-
-
Karger, R.1
Donner-Banzhoff, N.2
Muller, H.-H.3
Kretschmer, V.4
Hunink, M.5
-
33
-
-
33645557848
-
Platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet function
-
Hayward C P., Harrison P, Cattaneo M, Ortel T L., Rao A K. Platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet function. J Thromb Haemost 2006 4 312-319
-
(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
-
34
-
-
33646794952
-
Platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet functiona rebuttal
-
Kratzer M AA, Kretschmer V. Platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet functiona rebuttal. J Thromb Haemost 2006 4 1429-1431
-
(2006)
J Thromb Haemost
, vol.4
, pp. 1429-1431
-
-
Kratzer, M.A.1
Kretschmer, V.2
-
35
-
-
33646800154
-
More on: Platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet function
-
6
-
Koscielny J, Kiesewetter H, von Tempelhoff G F. More on: platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet function. J Thromb Haemost 2006 4 6 1426-1427, discussion 14281434
-
(2006)
J Thromb Haemost
, vol.4
, pp. 1426-1427
-
-
Koscielny, J.1
Kiesewetter, H.2
Von Tempelhoff, G.F.3
-
36
-
-
0031568828
-
A new method for quantitative analysis of whole blood platelet interaction with extracellular matrix under flow conditions
-
DOI 10.1016/S0049-3848(97)00014-5, PII S0049384897000145
-
Varon D, Dardik R, Shenkman B et al. A new method for quantitative analysis of whole blood platelet interaction with extracellular matrix under flow conditions. Thromb Res 1997 85 4 283-294 (Pubitemid 27143804)
-
(1997)
Thrombosis Research
, vol.85
, Issue.4
, pp. 283-294
-
-
Varon, D.1
Dardik, R.2
Shenkman, B.3
Kotev-Emeth, S.4
Farzame, N.5
Tamarin, I.6
Savion, N.7
-
37
-
-
77449152531
-
Evaluation of children with a suspected bleeding disorder applying the Impact-R [Cone and Plate(Let) Analyzer]
-
Revel-Vilk S, Varon D, Shai E et al. Evaluation of children with a suspected bleeding disorder applying the Impact-R [Cone And Plate(Let) Analyzer]. J Thromb Haemost 2009 7 1990-1996
-
(2009)
J Thromb Haemost
, vol.7
, pp. 1990-1996
-
-
Revel-Vilk, S.1
Varon, D.2
Shai, E.3
-
38
-
-
10744229532
-
Thrombin generation in platelet-poor plasma is normal in patients with hereditary mucocutaneous haemorrhages
-
DOI 10.1159/000071639
-
Quiroga T, Goycoolea M, Giesen P L. et al. Thrombin generation in platelet-poor plasma is normal in patients with hereditary mucocutaneous haemorrhages. Pathophysiol Haemost Thromb 2003 33 1 30-35 (Pubitemid 37449293)
-
(2003)
Pathophysiology of Haemostasis and Thrombosis
, vol.33
, Issue.1
, pp. 30-35
-
-
Quiroga, T.1
Goycoolea, M.2
Giesen, P.L.A.3
Morales, M.4
Munoz, B.5
Aranda, E.6
Rodriguez, S.7
Panes, O.8
Martinez, C.9
Pereira, J.10
Mezzano, D.11
-
39
-
-
29244452910
-
The influence of the haematocrit on primary haemostasis in vitro
-
DOI 10.1160/TH05-06-0424
-
Eugster M, Reinhart W H. The influence of the haematocrit on primary haemostasis in vitro. Thromb Haemost 2005 94 6 1213-1218 (Pubitemid 41819618)
-
(2005)
Thrombosis and Haemostasis
, vol.94
, Issue.6
, pp. 1213-1218
-
-
Eugster, M.1
Reinhart, W.H.2
-
40
-
-
0036280910
-
Assessment of thrombocytopenic disorders using the platelet function analyzer (PFA-100®)
-
DOI 10.1046/j.1365-2141.2002.03511.x
-
Carcao M D., Blanchette V S., Stephens D et al. Assessment of thrombocytopenic disorders using the Platelet Function Analyzer (PFA-100). Br J Haematol 2002 117 4 961-964 (Pubitemid 34639263)
-
(2002)
British Journal of Haematology
, vol.117
, Issue.4
, pp. 961-964
-
-
Carcao, M.D.1
Blanchette, V.S.2
Stephens, D.3
He, L.4
Wakefield, C.D.5
Butchart, S.6
Christie, D.J.7
Rand, M.L.8
-
41
-
-
43249098361
-
Evidence-based diagnosis of type 1 von Willebrand disease: A Bayes theorem approach
-
8
-
Tosetto A, Castaman G, Rodeghiero F. Evidence-based diagnosis of type 1 von Willebrand disease: a Bayes theorem approach. Blood 2008 111 8 3998-4003
-
(2008)
Blood
, vol.111
, pp. 3998-4003
-
-
Tosetto, A.1
Castaman, G.2
Rodeghiero, F.3
-
42
-
-
4444364103
-
Rare bleeding disorder registry: Deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias
-
DOI 10.1111/j.1538-7836.2003.t01-1-00553.x
-
Acharya S S., Coughlin A, Dimichele D M., North American Rare Bleeding Disorder Study Group. Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost 2004 2 2 248-256 (Pubitemid 40186038)
-
(2004)
Journal of Thrombosis and Haemostasis
, vol.2
, Issue.2
, pp. 248-256
-
-
Acharya, S.S.1
Coughlin, A.2
Dimichele, D.M.3
Jublirer, S.J.4
Arden, D.5
Anderson, V.6
Biega, C.7
Bartolomeo, A.8
Bernstein, Z.9
Sweeney, J.10
Belling, L.11
Cohen, A.R.12
Butler, R.13
Cripe, T.14
DiMichele, D.15
Davis, C.16
Del Toro, G.17
Ewing, N.18
Forster, A.19
Flug, F.20
Bray, G.21
Guelcher, C.22
Green, D.23
Griggs, S.24
Serauer, C.L.25
Hawk, S.M.26
Harber, C.27
Husted, M.28
Haag, B.29
Heffner, M.30
Jayabose, S.31
Kasper, C.32
Kouides, P.A.33
Phatak, P.34
Kulzer, L.35
Konkle, B.36
Killian-Spence, R.37
Johnson, M.38
Kitchens, C.S.39
Lipton, R.A.40
Freeman-Nord, B.41
LynnPayne, M.42
Nugent, D.43
McDaniel, M.44
Maier, P.J.45
Massey, G.V.46
Moczygemba, D.47
Bockenstedt, P.L.48
Mathis, D.49
Marcus, J.50
Fligman, I.51
Ortiz, I.52
Sheth, S.53
Stewart, K.54
Gilchrist, G.L.55
Schmidt, K.56
Seeler, R.A.57
Joist, H.58
Becherer, P.59
Spath, M.60
Sennett, M.61
Shurin, S.62
Mitchell, D.63
Fahner, J.B.64
Sandon-Kleiboer, B.65
Turner, C.66
Burkatt, P.T.67
Tancabelic, J.68
Haliburton, J.69
Tarantino, M.70
Burnett, D.71
Kalwinsky, D.K.72
Uncaphin, D.73
Blatt, P.M.74
Wagner, M.75
White, E.76
Cohen, A.J.77
Whitworth-Smith, K.78
Warrier, I.79
Broxson, E.80
Davignon, G.81
Grass, C.82
Teitel, J.83
Poon, M.C.84
Israels, S.85
more..
-
43
-
-
65349161613
-
Major differences in bleeding symptoms between factor VII deficiency and hemophilia B
-
International Factor VII Deficiency Study Group 5
-
Bernardi F, Dolce A, Pinotti M et al, International Factor VII Deficiency Study Group. Major differences in bleeding symptoms between factor VII deficiency and hemophilia B. J Thromb Haemost 2009 7 5 774-779
-
(2009)
J Thromb Haemost
, vol.7
, pp. 774-779
-
-
Bernardi, F.1
Dolce, A.2
Pinotti, M.3
-
44
-
-
33745632764
-
Bleeding in carriers of hemophilia
-
DOI 10.1182/blood-2005-09-3879
-
Plug I, Mauser-Bunschoten E P., Bröcker-Vriends A H. et al. Bleeding in carriers of hemophilia. Blood 2006 108 1 52-56 (Pubitemid 43990612)
-
(2006)
Blood
, vol.108
, Issue.1
, pp. 52-56
-
-
Plug, I.1
Mauser-Bunschoten, E.P.2
Brocker-Vriends, A.H.J.T.3
Van Amstel, H.K.P.4
Van Der Bom, J.G.5
Van Diemen-Homan, J.E.M.6
Willemse, J.7
Rosendaal, F.R.8
-
45
-
-
55949088269
-
Factor XIII deficiency
-
6
-
Hsieh L, Nugent D. Factor XIII deficiency. Haemophilia 2008 14 6 1190-1200
-
(2008)
Haemophilia
, vol.14
, pp. 1190-1200
-
-
Hsieh, L.1
Nugent, D.2
-
46
-
-
67749130935
-
Combined factor v and factor VIII deficiency
-
4
-
Spreafico M, Peyvandi F. Combined factor V and factor VIII deficiency. Semin Thromb Hemost 2009 35 4 390-399
-
(2009)
Semin Thromb Hemost
, vol.35
, pp. 390-399
-
-
Spreafico, M.1
Peyvandi, F.2
-
47
-
-
83055187115
-
1
-
DOI 10.1111/j.1365-2516.2007.01643.x
-
Nichols W L., Hultin M B., James A H. et al. von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA). Haemophilia 2008 14 2 171-232 (Pubitemid 351343618)
-
(2008)
Haemophilia
, vol.14
, Issue.2
, pp. 171-232
-
-
Nichols, W.L.1
Hultin, M.B.2
James, A.H.3
Manco-Johnson, M.J.4
Montgomery, R.R.5
Ortel, T.L.6
Rick, M.E.7
Sadler, J.E.8
Weinstein, M.9
Yawn, B.P.10
-
48
-
-
33846201270
-
The gray platelet syndrome: Clinical spectrum of the disease
-
DOI 10.1016/j.blre.2005.12.003, PII S0268960X05000718
-
Nurden A T., Nurden P. The gray platelet syndrome: clinical spectrum of the disease. Blood Rev 2007 21 1 21-36 (Pubitemid 46097190)
-
(2007)
Blood Reviews
, vol.21
, Issue.1
, pp. 21-36
-
-
Nurden, A.T.1
Nurden, P.2
-
50
-
-
0042808205
-
Inherited defects in platelet signaling mechanisms
-
4
-
Rao A K. Inherited defects in platelet signaling mechanisms. J Thromb Haemost 2003 1 4 671-681
-
(2003)
J Thromb Haemost
, vol.1
, pp. 671-681
-
-
Rao, A.K.1
-
51
-
-
67650581556
-
Recent advances in understanding the pathophysiology of Wiskott-Aldrich syndrome
-
25
-
Bosticardo M, Marangoni F, Aiuti A, Villa A, Grazia Roncarolo M. Recent advances in understanding the pathophysiology of Wiskott-Aldrich syndrome. Blood 2009 113 25 6288-6295
-
(2009)
Blood
, vol.113
, pp. 6288-6295
-
-
Bosticardo, M.1
Marangoni, F.2
Aiuti, A.3
Villa, A.4
Grazia Roncarolo, M.5
-
52
-
-
77951460081
-
X-linked thrombocytopenia (XLT) due to WAS mutations: Clinical characteristics, long-term outcome, and treatment options
-
16
-
Albert M H., Bittner T C., Nonoyama S et al. X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options. Blood 2010 115 16 3231-3238
-
(2010)
Blood
, vol.115
, pp. 3231-3238
-
-
Albert, M.H.1
Bittner, T.C.2
Nonoyama, S.3
-
53
-
-
74849107151
-
Insights into familial platelet disorder with propensity to myeloid malignancy (FPD/AML)
-
2
-
Owen C. Insights into familial platelet disorder with propensity to myeloid malignancy (FPD/AML). Leuk Res 2010 34 2 141-142
-
(2010)
Leuk Res
, vol.34
, pp. 141-142
-
-
Owen, C.1
-
54
-
-
66949177954
-
Advances in the understanding of congenital amegakaryocytic thrombocytopenia
-
1
-
Ballmaier M, Germeshausen M. Advances in the understanding of congenital amegakaryocytic thrombocytopenia. Br J Haematol 2009 146 1 3-16
-
(2009)
Br J Haematol
, vol.146
, pp. 3-16
-
-
Ballmaier, M.1
Germeshausen, M.2
-
55
-
-
0842330260
-
Inherited thrombocytopenias: Toward a molecular understanding of disorders of platelet production
-
DOI 10.1097/00008480-200402000-00005
-
Geddis A E., Kaushansky K. Inherited thrombocytopenias: toward a molecular understanding of disorders of platelet production. Curr Opin Pediatr 2004 16 1 15-22 (Pubitemid 38168156)
-
(2004)
Current Opinion in Pediatrics
, vol.16
, Issue.1
, pp. 15-22
-
-
Geddis, A.E.1
Kaushansky, K.2
-
57
-
-
37349121856
-
Bernard-Soulier syndrome: An inherited platelet disorder
-
Pham A, Wang J. Bernard-Soulier syndrome: an inherited platelet disorder. Arch Pathol Lab Med 2007 131 12 1834-1836 (Pubitemid 350294586)
-
(2007)
Archives of Pathology and Laboratory Medicine
, vol.131
, Issue.12
, pp. 1834-1836
-
-
Pham, A.1
Wang, J.2
-
58
-
-
23944466027
-
Macrothrombocytopenia in velocardiofacial syndrome
-
3
-
Pallotta R, Evangelista V, Margaglione M, Bucci I, Saponari A. Macrothrombocytopenia in velocardiofacial syndrome. J Thromb Haemost 2005 3 3 601-603
-
(2005)
J Thromb Haemost
, vol.3
, pp. 601-603
-
-
Pallotta, R.1
Evangelista, V.2
Margaglione, M.3
Bucci, I.4
Saponari, A.5
-
59
-
-
43149092271
-
Phenotypic identification of platelet-type von Willebrand disease and its discrimination from type 2B von Willebrand disease: A question of 2B or not 2B? A story of nonidentical twins? or two sides of a multidenominational or multifaceted primary-hemostasis coin
-
1
-
Favaloro E J. Phenotypic identification of platelet-type von Willebrand disease and its discrimination from type 2B von Willebrand disease: a question of 2B or not 2B? A story of nonidentical twins? Or two sides of a multidenominational or multifaceted primary-hemostasis coin? Semin Thromb Hemost 2008 34 1 113-127
-
(2008)
Semin Thromb Hemost
, vol.34
, pp. 113-127
-
-
Favaloro, E.J.1
-
60
-
-
0016782782
-
Mediterranean macrothrombocytopenia
-
2
-
Behrens W E. Mediterranean macrothrombocytopenia. Blood 1975 46 2 199-208
-
(1975)
Blood
, vol.46
, pp. 199-208
-
-
Behrens, W.E.1
-
61
-
-
84255202651
-
-
Pagon R. A. Bird T. D. Dolan C. R. Stephens K. eds. GeneReviews [Internet] University of Washington, Seattle, 2006
-
Kacena M A., Kirk J, Chou S T., Weiss M J., Raskind W H. GATA1-related X-linked cytopenia. In: Pagon R A. Bird T D. Dolan C R. Stephens K eds. GeneReviews [Internet]. University of Washington, Seattle, 2006
-
GATA1-related X-linked Cytopenia
-
-
Kacena, M.A.1
Kirk, J.2
Chou, S.T.3
Weiss, M.J.4
Raskind, W.H.5
-
62
-
-
78649744166
-
Gray platelet syndrome: Natural history of a large patient cohort and locus assignment to chromosome 3p
-
23
-
Gunay-Aygun M, Zivony-Elboum Y, Gumruk F et al. Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p. Blood 2010 116 23 4990-5001
-
(2010)
Blood
, vol.116
, pp. 4990-5001
-
-
Gunay-Aygun, M.1
Zivony-Elboum, Y.2
Gumruk, F.3
|