Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
ADAMTS13 activity in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: relation to presenting features and clinical outcomes in a prospective cohort of 142 patients.
|
Blood
|
2003
|
3.88
|
2
|
Survival and relapse in patients with thrombotic thrombocytopenic purpura.
|
Blood
|
2009
|
3.18
|
3
|
von Willebrand factor-mediated platelet adhesion is critical for deep vein thrombosis in mouse models.
|
Blood
|
2010
|
2.82
|
4
|
Elevated nucleosome levels in systemic inflammation and sepsis.
|
Crit Care Med
|
2003
|
2.76
|
5
|
Von Willebrand factor-cleaving protease (ADAMTS13) in thrombocytopenic disorders: a severely deficient activity is specific for thrombotic thrombocytopenic purpura.
|
Blood
|
2002
|
1.93
|
6
|
Pancreatitis preceding acute episodes of thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: report of five patients with a systematic review of published reports.
|
Haematologica
|
2007
|
1.87
|
7
|
Circulating DNA and myeloperoxidase indicate disease activity in patients with thrombotic microangiopathies.
|
Blood
|
2012
|
1.87
|
8
|
Epitope mapping of ADAMTS13 autoantibodies in acquired thrombotic thrombocytopenic purpura.
|
Blood
|
2004
|
1.67
|
9
|
Rapid determination of anti-heparin/platelet factor 4 antibody titers in the diagnosis of heparin-induced thrombocytopenia.
|
Am J Med
|
2003
|
1.64
|
10
|
Stability of coagulation assays performed in plasma from citrated whole blood transported at ambient temperature.
|
Thromb Haemost
|
2008
|
1.50
|
11
|
Pregnancy outcomes following recovery from acquired thrombotic thrombocytopenic purpura.
|
Blood
|
2014
|
1.47
|
12
|
Diagnostic criteria for hematopoietic stem cell transplant-associated microangiopathy: results of a consensus process by an International Working Group.
|
Haematologica
|
2007
|
1.39
|
13
|
Cloning, expression, and functional characterization of the von Willebrand factor-cleaving protease (ADAMTS13).
|
Blood
|
2002
|
1.29
|
14
|
ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases.
|
Blood
|
2005
|
1.27
|
15
|
Decreasing frequency of plasma exchange complications in patients treated for thrombotic thrombocytopenic purpura-hemolytic uremic syndrome, 1996 to 2011.
|
Transfusion
|
2012
|
1.27
|
16
|
Fatal congenital thrombotic thrombocytopenic purpura with apparent ADAMTS13 inhibitor: in vitro inhibition of ADAMTS13 activity by hemoglobin.
|
Blood
|
2004
|
1.20
|
17
|
C1-inhibitor in patients with severe sepsis and septic shock: beneficial effect on renal dysfunction.
|
Crit Care Med
|
2002
|
1.14
|
18
|
Multiple major morbidities and increased mortality during long-term follow-up after recovery from thrombotic thrombocytopenic purpura.
|
Blood
|
2013
|
1.13
|
19
|
Clinical outcomes after platelet transfusions in patients with thrombotic thrombocytopenic purpura.
|
Transfusion
|
2009
|
1.09
|
20
|
Polypharmacy is associated with an increased risk of bleeding in elderly patients with venous thromboembolism.
|
J Gen Intern Med
|
2014
|
1.02
|
21
|
Elevated levels of plasma prekallikrein, high molecular weight kininogen and factor XI in coronary heart disease.
|
Atherosclerosis
|
2002
|
0.99
|
22
|
Is factor V Leiden a risk factor for thrombotic microangiopathies without severe ADAMTS 13 deficiency?
|
Thromb Haemost
|
2005
|
0.99
|
23
|
Evidence for a role of anti-ADAMTS13 autoantibodies despite normal ADAMTS13 activity in recurrent thrombotic thrombocytopenic purpura.
|
Haematologica
|
2011
|
0.99
|
24
|
Effect of low-molecular weight dextran sulfate on coagulation and platelet function tests.
|
Thromb Res
|
2002
|
0.98
|
25
|
ADAMTS13 activity in sickle cell disease.
|
Am J Hematol
|
2006
|
0.95
|
26
|
ADAMTS13 gene defects in two brothers with constitutional thrombotic thrombocytopenic purpura and normalization of von Willebrand factor-cleaving protease activity by recombinant human ADAMTS13.
|
Br J Haematol
|
2003
|
0.92
|
27
|
Different disparities of gender and race among the thrombotic thrombocytopenic purpura and hemolytic-uremic syndromes.
|
Am J Hematol
|
2010
|
0.92
|
28
|
D-dimers predict stroke subtype when assessed early.
|
Cerebrovasc Dis
|
2009
|
0.92
|
29
|
von Willebrand factor-cleaving protease (ADAMTS-13) activity determination in the diagnosis of thrombotic microangiopathies: the Swiss experience.
|
Semin Hematol
|
2004
|
0.92
|
30
|
Cognitive deficits after recovery from thrombotic thrombocytopenic purpura.
|
Transfusion
|
2009
|
0.92
|
31
|
Platelets: thrombotic thrombocytopenic purpura.
|
Hematology Am Soc Hematol Educ Program
|
2002
|
0.91
|
32
|
Initial experience from a double-blind, placebo-controlled, clinical outcome study of ARC1779 in patients with thrombotic thrombocytopenic purpura.
|
Am J Hematol
|
2012
|
0.91
|
33
|
Frequency and significance of HIV infection among patients diagnosed with thrombotic thrombocytopenic purpura.
|
Clin Infect Dis
|
2009
|
0.91
|
34
|
Blood group O and black race are independent risk factors for thrombotic thrombocytopenic purpura associated with severe ADAMTS13 deficiency.
|
Transfusion
|
2011
|
0.90
|
35
|
The Swiss cohort of elderly patients with venous thromboembolism (SWITCO65+): rationale and methodology.
|
J Thromb Thrombolysis
|
2013
|
0.90
|
36
|
Thrombotic microangiopathic syndromes associated with drugs, HIV infection, hematopoietic stem cell transplantation and cancer.
|
Presse Med
|
2012
|
0.88
|
37
|
The Oklahoma Thrombotic Thrombocytopenic Purpura-Hemolytic Uremic Syndrome Registry: the Swiss connection.
|
Eur J Haematol
|
2008
|
0.87
|
38
|
Dosing lepirudin in patients with heparin-induced thrombocytopenia and normal or impaired renal function: a single-center experience with 68 patients.
|
Blood
|
2008
|
0.86
|
39
|
A common origin of the 4143insA ADAMTS13 mutation.
|
Thromb Haemost
|
2006
|
0.86
|
40
|
Acquired thrombotic thrombocytopenic purpura: ADAMTS13 activity, anti-ADAMTS13 autoantibodies and risk of recurrent disease.
|
Haematologica
|
2008
|
0.86
|
41
|
Familial acquired thrombotic thrombocytopenic purpura: ADAMTS13 inhibitory autoantibodies in identical twins.
|
Blood
|
2004
|
0.86
|
42
|
Contact system activation in human sepsis - 47kD HK, a marker of sepsis severity?
|
Swiss Med Wkly
|
2008
|
0.85
|
43
|
A first case of congenital TTP on the African continent due to a new homozygous mutation in the catalytic domain of ADAMTS13.
|
Ann Hematol
|
2008
|
0.85
|
44
|
Titre of anti-heparin/PF4-antibodies and extent of in vivo activation of the coagulation and fibrinolytic systems.
|
Thromb Haemost
|
2004
|
0.85
|
45
|
Plasma therapy in thrombotic thrombocytopenic purpura: review of the literature and the Bern experience in a subgroup of patients with severe acquired ADAMTS-13 deficiency.
|
Semin Hematol
|
2004
|
0.84
|
46
|
Use of the pentasaccharide fondaparinux as an anticoagulant during haemodialysis.
|
Thromb Haemost
|
2007
|
0.84
|
47
|
Sporadic bloody diarrhoea-associated thrombotic thrombocytopenic purpura-haemolytic uraemic syndrome: an adult and paediatric comparison.
|
Br J Haematol
|
2008
|
0.84
|
48
|
Rituximab for acute plasma-refractory thrombotic thrombocytopenic purpura. A case report and concise review of the literature.
|
Swiss Med Wkly
|
2007
|
0.81
|
49
|
Factor XIII in severe sepsis and septic shock.
|
Thromb Res
|
2006
|
0.81
|
50
|
Prekallikrein deficiency: the characteristic normalization of the severely prolonged aPTT following increased preincubation time is due to autoactivation of factor XII.
|
Thromb Res
|
2002
|
0.81
|
51
|
Design and establishment of a biobank in a multicenter prospective cohort study of elderly patients with venous thromboembolism (SWITCO65+).
|
J Thromb Thrombolysis
|
2013
|
0.80
|
52
|
Rapid exclusion or confirmation of heparin-induced thrombocytopenia: a single-center experience with 1,291 patients.
|
Haematologica
|
2011
|
0.80
|
53
|
Splenectomy in relapsing and plasma-refractory acquired thrombotic thrombocytopenic purpura.
|
Haematologica
|
2004
|
0.80
|
54
|
Evaluation of a Platelet Function Analyser (PFA-100) in patients with a bleeding tendency.
|
Swiss Med Wkly
|
2002
|
0.79
|
55
|
Hemostatic risk factors in ischemic stroke.
|
Thromb Haemost
|
2003
|
0.78
|
56
|
Role of ADAMTS13 in the pathogenesis, diagnosis, and treatment of thrombotic thrombocytopenic purpura.
|
Hematology Am Soc Hematol Educ Program
|
2012
|
0.78
|
57
|
Massive muscle haematoma three months after starting vitamin K antagonist therapy for deep-vein thrombosis in an antithrombin deficient patient: another case of factor IX propeptide mutation.
|
Thromb Haemost
|
2011
|
0.77
|
58
|
Assays of von Willebrand factor-cleaving protease: a test for diagnosis of familial and acquired thrombotic thrombocytopenic purpura.
|
Semin Thromb Hemost
|
2002
|
0.77
|
59
|
Rumpel-Leede sign in thrombocytopenia due to Epstein-Barr virus-induced mononucleosis.
|
Br J Haematol
|
2009
|
0.77
|
60
|
The von Willebrand factor-cleaving protease (ADAMTS-13) and the diagnosis of thrombotic thrombocytopenic purpura (TTP).
|
Pathophysiol Haemost Thromb
|
2005
|
0.76
|
61
|
Effective therapy with tranexamic acid in a case of chronic disseminated intravascular coagulation with acquired alpha2-antiplasmin deficiency associated with AL amyloidosis.
|
Thromb Haemost
|
2009
|
0.76
|
62
|
Hemophilia A pseudoaneurysm in a patient with high responding inhibitors complicating total knee arthroplasty: embolization: a cost-reducing alternative to medical therapy.
|
Cardiovasc Intervent Radiol
|
2006
|
0.76
|
63
|
Discrepant activity levels of von Willebrand factor-cleaving protease (ADAMTS-13) in congenital thrombotic thrombocytopenic purpura.
|
Blood
|
2003
|
0.75
|
64
|
Thromboembolism in patients with congenital afibrinogenaemia. Long-term observational data and systematic review.
|
Thromb Haemost
|
2016
|
0.75
|
65
|
On the dosing of lepirudin.
|
Br J Clin Pharmacol
|
2011
|
0.75
|
66
|
Prospective cross-sectional study of haemostatic factors in patients with and without coronary artery disease.
|
Blood Coagul Fibrinolysis
|
2003
|
0.75
|
67
|
Low-dose recombinant factor VIIa for massive bleeding: a single centre observational cohort study with 73 patients.
|
Swiss Med Wkly
|
2011
|
0.75
|
68
|
The impact of congenital thrombotic thrombocytopenic purpura on pregnancy complications.
|
Thromb Haemost
|
2014
|
0.75
|
69
|
Concomitant treatment with lamivudine renders cladribine inactive by inhibition of its phosphorylation.
|
Br J Haematol
|
2008
|
0.75
|
70
|
[Thrombotic thrombocytopenic purpura--an often missed diagnosis].
|
Rev Med Suisse
|
2014
|
0.75
|
71
|
Derivation and validation of a novel bleeding risk score for elderly patients with venous thromboembolism on extended anticoagulation.
|
Thromb Haemost
|
2017
|
0.75
|
72
|
May-Thurner syndrome: missed diagnosis and missed early treatment?
|
Hamostaseologie
|
2017
|
0.75
|
73
|
Congenital thrombotic thrombocytopenic purpura caused by new compound heterozygous mutations of the ADAMTS13 gene.
|
Eur J Haematol
|
2013
|
0.75
|