Pål André Holme
- Group leader, professor; MD, PhD
- +47 23 07 36 11
Publications 2024
Human papilloma virus vaccine induced thrombocytopenia accompanied by a wide spectrum of reversible inflammatory responses - a case report
Scand J Clin Lab Invest, 84 (6), 425-427
DOI 10.1080/00365513.2024.2400663, PubMed 39264796
Moving towards Normalization of haemostasis and health equity: Evolving treatment goals for haemophilia A
Haemophilia, 30 (5), 1109-1114
DOI 10.1111/hae.15031, PubMed 38986684
Safety and efficacy of damoctocog alfa pegol prophylaxis in patients with severe haemophilia A: Results of an interventional, post-marketing study
Haemophilia, 30 (2), 388-394
DOI 10.1111/hae.14930, PubMed 38229269
Superior Prophylactic Effectiveness of a Recombinant FVIIIFc Over Standard Half-Life FVIII in Hemophilia A: A-SURE Study
Eur J Haematol (in press)
DOI 10.1111/ejh.14309, PubMed 39434416
The association between unemployment and treatment among adults with hemophilia
Res Pract Thromb Haemost, 8 (5), 102514
DOI 10.1016/j.rpth.2024.102514, PubMed 39188890
Damoctocog Alfa Pegol, a PEGylated B-domain Deleted Recombinant Extended Half-life Factor VIII for the Treatment of Hemophilia A: A Product Review
Drugs R D, 24 (3), 359-381
DOI 10.1007/s40268-024-00481-7, PubMed 39162954
Long-Term Efficacy and Safety of Damoctocog Alfa Pegol Prophylaxis in Patients with Haemophilia A Aged 12-<18 Years at Enrolment into PROTECT VIII
Acta Haematol, 1-10 (in press)
DOI 10.1159/000538702, PubMed 38599195
Publications 2023
Impact of timing of prophylaxis commencement, F8 genotype and age on factor consumption and health-related quality of life in patients with severe haemophilia A
Haemophilia, 29 (4), 1032-1038
DOI 10.1111/hae.14806, PubMed 37252898
Infrastructural considerations of implementing gene therapy for hemophilia in the Nordic context
Ther Adv Hematol, 14, 20406207231202306
DOI 10.1177/20406207231202306, PubMed 37859645
Real-world data in patients with congenital hemophilia and inhibitors: final data from the FEIBA Global Outcome (FEIBA GO) study
Ther Adv Hematol, 14, 20406207231184323
DOI 10.1177/20406207231184323, PubMed 37529276
Prevalence of COVID-19 related hospitalizations and mortality in adults aged ≥40 years with haemophilia: A survey from Europe
Haemophilia, 29 (3), 913-916
DOI 10.1111/hae.14761, PubMed 36802089
Report on 4 cases with decreased recovery due to neutralizing antibodies specific for PEGylated recombinant factor VIII
J Thromb Haemost, 21 (10), 2771-2775
DOI 10.1016/j.jtha.2023.07.019, PubMed 37543216
Elevated FVIII levels in hereditary hemorrhagic telangiectasia: Implications for clinical management
Laryngoscope Investig Otolaryngol, 9 (1), e1196
DOI 10.1002/lio2.1196, PubMed 38362186
Physical activity in Norwegian teenagers and young adults with haemophilia A compared to general population peers
Haemophilia, 29 (2), 658-667
DOI 10.1111/hae.14752, PubMed 36723510
Factors associated with physical activity in young people with haemophilia A on prophylaxis
Haemophilia, 29 (3), 900-909
DOI 10.1111/hae.14776, PubMed 36913380
Health-related quality of life and physical activity in Nordic patients with moderate haemophilia A and B (the MoHem study)
Haemophilia, 30 (1), 98-105
DOI 10.1111/hae.14899, PubMed 37983883
Efficacy and safety of damoctocog alfa pegol prophylaxis in patients ⩾40 years with severe haemophilia A and comorbidities: post hoc analysis from the PROTECT VIII study
Ther Adv Hematol, 14, 20406207231166779
DOI 10.1177/20406207231166779, PubMed 37113811
von Willebrand factor, ADAMTS-13, and thrombospondin 1 in relation to clinical outcomes in elderly patients with a recent myocardial infarction
Res Pract Thromb Haemost, 7 (4), 100164
DOI 10.1016/j.rpth.2023.100164, PubMed 37255854
Publications 2022
Clinical outcome and adherence rate in Scandinavian patients with intermediate-intensity prophylaxis before and after the switch of standard half-life FVIII products to BAY 81-8973
Haemophilia, 28 (2), 223-229
DOI 10.1111/hae.14489, PubMed 35005818
Elevated NETs and Calprotectin Levels after ChAdOx1 nCoV-19 Vaccination Correlate with the Severity of Side Effects
Vaccines (Basel), 10 (8)
DOI 10.3390/vaccines10081267, PubMed 36016155
Factor IX antibodies and tolerance in hemophilia B in the Nordic countries - The impact of F9 variants and complications
Thromb Res, 217, 22-32
DOI 10.1016/j.thromres.2022.06.015, PubMed 35842956
Applicability of the European Society of Cardiology Guidelines on the management of acute coronary syndromes to older people with haemophilia A - A modified Delphi consensus by the ADVANCE Working Group
Haemophilia, 29 (1), 21-32
DOI 10.1111/hae.14674, PubMed 36271497
Bone mineral density in haemophilia - a multicentre study evaluating the impact of different replacement regimens
Haemophilia, 28 (2), 239-246
DOI 10.1111/hae.14487, PubMed 34994489
Surgical outcomes in patients with haemophilia A or B receiving extended half-life recombinant factor VIII and IX Fc fusion proteins: Real-world experience in the Nordic countries
Haemophilia, 28 (5), 713-719
DOI 10.1111/hae.14585, PubMed 35575446
Comparison of free-living physical activity measurements between ActiGraph GT3X-BT and Fitbit Charge 3 in young people with haemophilia
Haemophilia, 28 (6), e172-e180
DOI 10.1111/hae.14624, PubMed 35830613
Vaccine associated benign headache and cutaneous hemorrhage after ChAdOx1 nCoV-19 vaccine: A cohort study
J Stroke Cerebrovasc Dis, 32 (1), 106860
DOI 10.1016/j.jstrokecerebrovasdis.2022.106860, PubMed 36403363
Platelet function testing: Current practice among clinical centres in Northern Europe
Haemophilia, 28 (4), 642-648
DOI 10.1111/hae.14578, PubMed 35510959
Anti-PF4/polyanion antibodies in COVID-19 patients are associated with disease severity and pulmonary pathology
Platelets, 33 (4), 640-644
DOI 10.1080/09537104.2022.2042238, PubMed 35225150
Genetic Variation in ADAMTS13 is Related to VWF Levels, Atrial Fibrillation and Cerebral Ischemic Events
Clin Appl Thromb Hemost, 28, 10760296221141893
DOI 10.1177/10760296221141893, PubMed 36474435
Publications 2021
New Inhibitors in the Ageing Population: A Retrospective, Observational, Cohort Study of New Inhibitors in Older People with Hemophilia
Thromb Haemost, 122 (6), 905-912
DOI 10.1055/a-1642-4067, PubMed 34507368
Immune complexes, innate immunity, and NETosis in ChAdOx1 vaccine-induced thrombocytopenia
Eur Heart J, 42 (39), 4064-4072
DOI 10.1093/eurheartj/ehab506, PubMed 34405870
Immune tolerance induction in the era of emicizumab - still the first choice for patients with haemophilia A and inhibitors?
Haemophilia, 28 (2), 215-222
DOI 10.1111/hae.14470, PubMed 34918839
Concomitant use of bypassing agents with emicizumab for people with haemophilia A and inhibitors undergoing surgery
Haemophilia, 27 (4), 519-530
DOI 10.1111/hae.14322, PubMed 33988293
Thrombosis and thrombocytopenia after HPV vaccination
J Thromb Haemost, 20 (3), 700-704
DOI 10.1111/jth.15604, PubMed 34817130
Haemophilia early arthropathy detection with ultrasound and haemophilia joint health score in the moderate haemophilia (MoHem) study
Haemophilia, 27 (2), e253-e259
DOI 10.1111/hae.14245, PubMed 33550602
Bleeding phenotype of patients with moderate haemophilia A and B assessed by thromboelastometry and thrombin generation
Haemophilia, 27 (5), 793-801
DOI 10.1111/hae.14355, PubMed 34106506
Confirmed long-term safety and efficacy of prophylactic treatment with BAY 94-9027 in severe haemophilia A: final results of the PROTECT VIII extension study
Haemophilia, 27 (3), e347-e356
DOI 10.1111/hae.14297, PubMed 33818853
Investigation of the Optimal Dose aPCC in Reversing the Effect of Factor Xa Inhibitors-An In Vitro Study
Clin Appl Thromb Hemost, 27, 10760296211021156
DOI 10.1177/10760296211021156, PubMed 34060371
The effect of emicizumab and bypassing agents in patients with hemophilia - An in vitro study
Res Pract Thromb Haemost, 5 (5), e12561
DOI 10.1002/rth2.12561, PubMed 34263107
Thrombosis and Thrombocytopenia after ChAdOx1 nCoV-19 Vaccination
N Engl J Med, 384 (22), 2124-2130
DOI 10.1056/NEJMoa2104882, PubMed 33835768
Vaccine Induced Immune Thrombotic Thrombocytopenia Causing a Severe Form of Cerebral Venous Thrombosis With High Fatality Rate: A Case Series
Front Neurol, 12, 721146
DOI 10.3389/fneur.2021.721146, PubMed 34393988
Publications 2020
Pharmacokinetics and pharmacodynamics of a recombinant fusion protein linking activated coagulation factor VII with human albumin (rVIIa-FP) in patients with congenital FVII deficiency
Hematology, 25 (1), 17-25
DOI 10.1080/16078454.2019.1700329, PubMed 31852380
Management of comorbidities in haemophilia
Haemophilia, 27 Suppl 3, 37-45
DOI 10.1111/hae.14013, PubMed 32476243
Joint health and treatment modalities in Nordic patients with moderate haemophilia A and B - The MoHem study
Haemophilia, 26 (5), 891-897
DOI 10.1111/hae.14114, PubMed 33021747
Macroscopic hematuria as a risk factor for hypertension in ageing people with hemophilia and a family history of hypertension
Medicine (Baltimore), 99 (9), e19339
DOI 10.1097/MD.0000000000019339, PubMed 32118768
Hematuria in aging men with hemophilia: Association with factor prophylaxis
Res Pract Thromb Haemost, 4 (2), 309-317
DOI 10.1002/rth2.12298, PubMed 32110762
Long-term outcomes of patients treated with rituximab as second-line treatment for adult immune thrombocytopenia - Follow-up of the RITP study
Br J Haematol, 191 (3), 460-465
DOI 10.1111/bjh.16672, PubMed 32342497
Publications 2019
[Surgical procedures in patients with severe haemophilia 1997–2014]
Tidsskr Nor Laegeforen, 139 (8)
DOI 10.4045/tidsskr.18.0592, PubMed 31062561
Surgical intervention in patients with severe bleeding disorder 1997-2014
Tidsskr. Nor. Laegeforen., 139 (8), 709-712
Fixed doses of N8-GP prophylaxis maintain moderate-to-mild factor VIII levels in the majority of patients with severe hemophilia A
Res Pract Thromb Haemost, 3 (3), 542-554
DOI 10.1002/rth2.12220, PubMed 31294338
BAY 94-9027 prophylaxis is efficacious and well tolerated for up to >5 years with extended dosing intervals: PROTECT VIII extension interim results
Haemophilia, 25 (6), 1011-1019
DOI 10.1111/hae.13853, PubMed 31621991
Evaluation of a standardized protocol for thrombin generation using the calibrated automated thrombogram: A Nordic study
Haemophilia, 25 (2), 334-342
DOI 10.1111/hae.13640, PubMed 30715788
The influence of rivaroxaban on markers of fibrinolysis and endothelial cell activation/injury in patients with venous thrombosis
Thromb Res, 177, 154-156
DOI 10.1016/j.thromres.2019.03.010, PubMed 30903875
Publications 2018
STIM1 R304W causes muscle degeneration and impaired platelet activation in mice
Cell Calcium, 76, 87-100
DOI 10.1016/j.ceca.2018.10.001, PubMed 30390422
Continuous infusion of simoctocog alfa in haemophilia A patients undergoing surgeries
Haemophilia, 25 (1), 54-59
DOI 10.1111/hae.13625, PubMed 30394617
The elevated prevalence of risk factors for chronic liver disease among ageing people with hemophilia and implications for treatment
Medicine (Baltimore), 97 (39), e12551
DOI 10.1097/MD.0000000000012551, PubMed 30278553
The impact of rivaroxaban on primary hemostasis in patients with venous thrombosis
Platelets, 31 (1), 43-47
DOI 10.1080/09537104.2018.1557618, PubMed 30569801
Activated prothrombin complex concentrate to reverse the factor Xa inhibitor (apixaban) effect before emergency surgery: a case series
J Med Case Rep, 12 (1), 138
DOI 10.1186/s13256-018-1660-9, PubMed 29764497
Publications 2017
The second Team Haemophilia Education Meeting, 2016, Frankfurt, Germany
Eur J Haematol, 98 Suppl 85, 1-15
DOI 10.1111/ejh.12828, PubMed 28101938
Continuous infusion of coagulation factor concentrates during intensive treatment
Haemophilia, 24 (1), 24-32
DOI 10.1111/hae.13331, PubMed 28873263
The association between health utility and joint status among people with severe haemophilia A: findings from the KAPPA register
Haemophilia, 23 (3), e180-e187
DOI 10.1111/hae.13231, PubMed 28393468
The reversal effect of prothrombin complex concentrate (PCC), activated PCC and recombinant activated factor VII against anticoagulation of Xa inhibitor
Thromb J, 15, 6
DOI 10.1186/s12959-017-0129-1, PubMed 28239301
The reversal effect of prothrombin complex concentrate (PCC), activated PCC and recombinant activated factor VII in apixaban-treated patients in vitro
Res Pract Thromb Haemost, 1 (1), 49-56
DOI 10.1002/rth2.12015, PubMed 30046673
Publications 2016
Complement activation is a crucial pathogenic factor in catastrophic antiphospholipid syndrome
Rheumatology (Oxford), 55 (7), 1337-9
DOI 10.1093/rheumatology/kew040, PubMed 27105662
How to compare cardiovascular disease and risk factors in elderly patients with haemophilia with the general population
Haemophilia, 22 (5), e406-16
DOI 10.1111/hae.13069, PubMed 27650262
Post-thrombotic syndrome after catheter-directed thrombolysis for deep vein thrombosis (CaVenT): 5-year follow-up results of an open-label, randomised controlled trial
Lancet Haematol, 3 (2), e64-71
DOI 10.1016/S2352-3026(15)00248-3, PubMed 26853645
Evaluation of the utility of the ISTH-BAT in haemophilia carriers: a multinational study
Haemophilia, 22 (6), 912-918
DOI 10.1111/hae.13089, PubMed 27868369
Publications 2015
Presentation and management of acute coronary syndromes among adult persons with haemophilia: results of an international, retrospective, 10-year survey
Haemophilia, 21 (5), 589-97
DOI 10.1111/hae.12652, PubMed 25689278
Rituximab as second-line treatment for adult immune thrombocytopenia (the RITP trial): a multicentre, randomised, double-blind, placebo-controlled trial
Lancet, 385 (9978), 1653-61
DOI 10.1016/S0140-6736(14)61495-1, PubMed 25662413
Hypertension, haematuria and renal functioning in haemophilia - a cross-sectional study in Europe
Haemophilia, 22 (2), 248-255
DOI 10.1111/hae.12847, PubMed 27880029
Should anti-inhibitor coagulant complex and tranexamic acid be used concomitantly?
Haemophilia, 21 (6), 709-14
DOI 10.1111/hae.12723, PubMed 26036756
Publications 2014
[Allogeneic stem-cell transplantation in adults 1985-2012: results and development]
Tidsskr Nor Laegeforen, 134 (16), 1569-75
DOI 10.4045/tidsskr.13.1415, PubMed 25178233
Adaptation of trustworthy guidelines developed using the GRADE methodology: a novel five-step process
Chest, 146 (3), 727-734
DOI 10.1378/chest.13-2828, PubMed 25180723
A dominant STIM1 mutation causes Stormorken syndrome
Hum Mutat, 35 (5), 556-64
DOI 10.1002/humu.22544, PubMed 24619930
Monitoring bypassing agent therapy - a prospective crossover study comparing thromboelastometry and thrombin generation assay
Haemophilia, 21 (2), 275-283
DOI 10.1111/hae.12570, PubMed 25521720
[A man in his 80s with muscle stiffness and skin bleeding]
Tidsskr Nor Laegeforen, 134 (10), 1058-61
DOI 10.4045/tidsskr.13.0817, PubMed 24865732
[Antithrombotic therapy in surgery]
Tidsskr Nor Laegeforen, 134 (9), 925
DOI 10.4045/tidsskr.13.1580, PubMed 24828716
Publications 2013
Increased volume of distribution for recombinant activated factor VII and longer plasma-derived factor VII half-life may explain their long lasting prophylactic effect
Thromb Res, 132 (2), 256-62
DOI 10.1016/j.thromres.2013.05.027, PubMed 23834817
Tranexamic acid as adjunct therapy to bypassing agents in haemophilia A patients with inhibitors
Haemophilia, 20 (3), 369-75
DOI 10.1111/hae.12318, PubMed 24251535
Use of thromboelastography and thrombin generation assay to predict clinical phenotype in patients with severe FVII deficiency
Haemophilia, 20 (1), 141-6
DOI 10.1111/hae.12256, PubMed 23992369
Pharmacodynamics of recombinant activated factor VII and plasma-derived factor VII in a cohort of severe FVII deficient patients
Thromb Res, 132 (1), 116-22
DOI 10.1016/j.thromres.2013.04.021, PubMed 23731565
Haemophilic arthropathy: long-term outcomes in 107 primary total knee arthroplasties
Knee, 21 (1), 147-50
DOI 10.1016/j.knee.2013.09.010, PubMed 24156923
Publications 2012
Continuous infusion in haemophilia: current practice in Europe
Haemophilia, 18 (5), 753-9
DOI 10.1111/j.1365-2516.2012.02810.x, PubMed 22530687
Combined treatment with APCC (FEIBA®) and tranexamic acid in patients with haemophilia A with inhibitors and in patients with acquired haemophilia A--a two-centre experience
Haemophilia, 18 (4), 544-9
DOI 10.1111/j.1365-2516.2012.02748.x, PubMed 22348384
Publications 2011
Long-term outcome after additional catheter-directed thrombolysis versus standard treatment for acute iliofemoral deep vein thrombosis (the CaVenT study): a randomised controlled trial
Lancet, 379 (9810), 31-8
DOI 10.1016/S0140-6736(11)61753-4, PubMed 22172244
Recurrent venous thrombosis, post-thrombotic syndrome and quality of life after catheter-directed thrombolysis in severe proximal deep vein thrombosis
J Thromb Haemost, 9 (6), 1261-3
DOI 10.1111/j.1538-7836.2011.04298.x, PubMed 21489133
Nordic Haemophilia Council's practical guidelines on diagnosis and management of von Willebrand disease
Semin Thromb Hemost, 37 (5), 495-502
DOI 10.1055/s-0031-1281034, PubMed 22102192
rFVIIa administered by continuous infusion during surgery in patients with severe congenital FVII deficiency
Haemophilia, 17 (5), 764-70
DOI 10.1111/j.1365-2516.2011.02596.x, PubMed 21707871
Recovery, survival, and function of transfused platelets and detection of platelet engraftment after allogeneic stem cell transplantation
Transfusion, 52 (6), 1321-32
DOI 10.1111/j.1537-2995.2011.03442.x, PubMed 22084943
Publications 2010
Non-genetic risk factors and the development of inhibitors in haemophilia: a comprehensive review and consensus report
Haemophilia, 16 (5), 747-66
DOI 10.1111/j.1365-2516.2010.02231.x, PubMed 20398077
[Immune thrombocytopenia--pathophysiology and treatment]
Tidsskr Nor Laegeforen, 130 (21), 2120-3
DOI 10.4045/tidsskr.09.1119, PubMed 21052113
Publications 2009
European curriculum for thrombosis and haemostasis
Haemophilia, 15 (1), 337-44
DOI 10.1111/j.1365-2516.2008.01836.x, PubMed 19149857
Catheter-directed thrombolysis vs. anticoagulant therapy alone in deep vein thrombosis: results of an open randomized, controlled trial reporting on short-term patency
J Thromb Haemost, 7 (8), 1268-75
DOI 10.1111/j.1538-7836.2009.03464.x, PubMed 19422443
Home treatment with bypassing products in inhibitor patients: a 7.5-year experience
Haemophilia, 15 (3), 727-32
DOI 10.1111/j.1365-2516.2009.02017.x, PubMed 19320748
FEIBA prophylaxis in haemophilia patients: a clinical update and treatment recommendations
Haemophilia, 16 (1), 80-9
DOI 10.1111/j.1365-2516.2009.02104.x, PubMed 19780845
Catheter-directed thrombolysis for treatment of deep venous thrombosis in the upper extremities
Cardiovasc Intervent Radiol, 32 (5), 980-7
DOI 10.1007/s00270-009-9655-y, PubMed 19641959
Publications 2008
[Allogeneic stem cell transplantation in acute myelogenous leukemia]
Tidsskr Nor Laegeforen, 128 (15), 1681-2; author reply 1682
PubMed 18704137
[Allogeneic stem cell transplantation in adults with acute lymphoblastic leukaemia]
Tidsskr Nor Laegeforen, 128 (22), 2563-6
PubMed 19023351
[A 40-year old woman with dizziness and vomiting]
Tidsskr Nor Laegeforen, 128 (12), 1413-5
PubMed 18584769
Hypercoagulability in patients with haematological neoplasia: no apparent initiation by tissue factor
Thromb Haemost, 99 (6), 1040-8
DOI 10.1160/TH07-09-0541, PubMed 18521506
Publications 2007
Catheter-directed Venous Thrombolysis in acute iliofemoral vein thrombosis--the CaVenT study: rationale and design of a multicenter, randomized, controlled, clinical trial (NCT00251771)
Am Heart J, 154 (5), 808-14
DOI 10.1016/j.ahj.2007.07.010, PubMed 17967583
[Deficient thrombosis prophylaxis]
Tidsskr Nor Laegeforen, 127 (9), 1176
PubMed 17479132
Factor eight inhibitor bypass activity (FEIBA) in the management of bleeds in hemophilia patients with high-titer inhibitors
Vasc Health Risk Manag, 3 (4), 527-31
PubMed 17969383
Publications 2005
Acquired haemophilia: management of bleeds and immune therapy to eradicate autoantibodies
Haemophilia, 11 (5), 510-5
DOI 10.1111/j.1365-2516.2005.01136.x, PubMed 16128896
Publications 1998
Enhanced activation of platelets with abnormal release of RANTES in human immunodeficiency virus type 1 infection
FASEB J, 12 (1), 79-89
DOI 10.1096/fasebj.12.1.79, PubMed 9438413
Microvesicles bind soluble fibrinogen, adhere to immobilized fibrinogen and coaggregate with platelets
Thromb Haemost, 79 (2), 389-94
PubMed 9493596
Shear-induced platelet activation and platelet microparticle formation in native human blood
Thromb Res, 92 (6 Suppl 2), S33-41
DOI 10.1016/s0049-3848(98)00158-3, PubMed 9886908
Publications 1997
Shear-induced platelet activation and platelet microparticle formation at blood flow conditions as in arteries with a severe stenosis
Arterioscler Thromb Vasc Biol, 17 (4), 646-53
DOI 10.1161/01.atv.17.4.646, PubMed 9108776
Publications 1996
Studies on human platelet-derived microvesicles: with special reference to their mode of formation, procoagulant properties and clinical relevance
Research Institute for Internal Medicine, Rikshospitalet,University of Oslo, Oslo, 1 b. (flere pag.)
BIBSYS 970050607, ISBN 82-7722-063-4
Glycoprotein IIb-IIIa on platelet-derived microparticles, and microparticle structures studied by electron microscopy, confocal laser microscopy and crossed radio-immunoelectrophoresis
Platelets, 7 (4), 207-14
DOI 10.3109/09537109609023580, PubMed 21043689
Publications 1995
Platelet-derived microvesicles and activated platelets express factor Xa activity
Blood Coagul Fibrinolysis, 6 (4), 302-10
DOI 10.1097/00001721-199506000-00002, PubMed 7548677
Stimulated Glanzmann's thrombasthenia platelets produced microvesicles. Microvesiculation correlates better to exposure of procoagulant surface than to activation of GPIIb-IIIa
Thromb Haemost, 74 (6), 1533-40
PubMed 8772233
The Fluid-phase SC5b-9 Terminal Complement Complex Binds to the GPIIb/IIIa Complex of Thrombin-stimulated Human Blood Platelets Inhibiting Platelet Aggregation
Platelets, 6 (3), 160-8
DOI 10.3109/09537109509013269, PubMed 21043620
Detection of biotinylated proteins in crossed immunoelectrophoresis gels: studies on platelet membrane receptors and microparticles
Electrophoresis, 16 (8), 1408-13
DOI 10.1002/elps.11501601233, PubMed 8529606
Publications 1994
Demonstration of platelet-derived microvesicles in blood from patients with activated coagulation and fibrinolysis using a filtration technique and western blotting
Thromb Haemost, 72 (5), 666-71
PubMed 7900071
Publications 1993
The difference between platelet and plasma FXIII used to study the mechanism of platelet microvesicle formation
Thromb Haemost, 70 (4), 681-6
PubMed 8115996