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Prothrombin and Factor V Mutations in Women with a History of Thrombosis during Pregnancy and the Puerperium

The New England journal of medicine, 2000-02, Vol.342 (6), p.374-380

2000

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Rotational thrombelastometry for the bedside monitoring of recombinant hirudin

Acta anaesthesiologica Scandinavica, 2008-03, Vol.52 (3), p.358-362

2008

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Rotation thromboelastography (ROTEM) parameters are influenced by age, gender, and oral contraception

Perfusion, 2011-07, Vol.26 (4), p.334-340

2011

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Monitoring of NOAC

Medizinische Klinik, Intensivmedizin und Notfallmedizin, 2017-03, Vol.112 (2), p.92-98

2017

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The G20210A prothrombin‐gene mutation and the plasminogen activator inhibitor (PAI‐1) 5G/5G genotype are associated with early onset of severe preeclampsia

Journal of thrombosis and haemostasis, 2005-04, Vol.3 (4), p.686-691

2005

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Prospective analysis after coronary-artery bypass grafting: platelet GP IIIa polymorphism (HPA-1b/PIA2) is a risk factor for bypass occlusion, myocardial infarction, and death

Thrombosis and haemostasis, 2000-03, Vol.83 (3), p.404-407

2000

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Polymorphism of platelet membrane glycoprotein IIIa: human platelet antigen 1b (HPA-1b/PlA2) is an inherited risk factor for premature myocardial infarction in coronary artery disease

Thrombosis and haemostasis, 1998-04, Vol.79 (4), p.731-735

1998

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Thrombophilia in pregnancy: venous thromboembolism, fetal loss, preeclampsia, intrauterine growth restriction

Hämostaseologie, 2008-12, Vol.28 (5), p.455

2008

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Associations between thrombophilic risk factors and determinants of atherosclerosis and inflammation in patients with non-arteritic anterior ischaemic optic neuropathy

Hämostaseologie, 2016, Vol.36 (1), p.46-54

2016

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Platelet-function analyzer closure times indicate shear stress-induced hemostatic abnormalities in patients with aortic valve stenosis and correlate with perioperative transfusion requirements

Perfusion, 2010-05, Vol.25 (3), p.153-158

2010

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Die Bedeutung thrombophiler Risikofaktoren bei Patienten mit arteriellen Thrombosen

Hämostaseologie, 2008, Vol.28 (3), p.120-129

Zotz, R. B.

2008

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Thrombophile Hämostasestörung in der Schwangerschaft: Thrombose, Abort, Präeklampsie, intrauterine Wachstumsretardierung

Hämostaseologie, 2008, Vol.28 (5), p.455-464

2008

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Antithrombotic prophylaxis for women with thrombophilia and pregnancy complications

Journal of thrombosis and haemostasis, 2004-07, Vol.2 (7), p.1182-1183

2004

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Monitoring von NOAK

Medizinische Klinik, Intensivmedizin und Notfallmedizin, 2017-03, Vol.112 (2), p.92-98

2017

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The international, prospective Glanzmann Thrombasthenia Registry: treatment and outcomes in surgical intervention

Haematologica (Roma), 2015-08, Vol.100 (8), p.1038

2015

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Thrombophilia and gestational venous thromboembolism

Thrombosis research, 2005-02, Vol.115 Suppl 1, p.99

2005

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Methylenetetrahydrofolate reductase gene polymorphism and glucocorticoid intake in children with ALL and aseptic osteonecrosis

Klinische Pädiatrie, 2003-11, Vol.215 (6), p.327-331

2003

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Rekombinanter Faktor VIIa bei Patienten mit Plättchenfunktionsstörungen oder Thrombozytopenien

Hämostaseologie, 2007, Vol.27 (4), p.251-262

2007

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Impact of thrombophilic risk factors in patients with arterial thromboses

Hämostaseologie, 2008, Vol.28 (3), p.120

Zotz, Rainer B

2008

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Genetic typing of human platelet antigen 1 (HPA‐1) by oligonucleotide ligation assay in a specific and reliable semi‐automated system

British journal of haematology, 1997-01, Vol.96 (1), p.198-203

1997

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Combined von Willebrand factor deficiency and factor XII deficiency

Thrombosis and haemostasis, 2000-03, Vol.83 (3), p.514-516

2000

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Das erworbene von-Willebrand-Syndrom

Deutsche medizinische Wochenschrift, 2004-07, Vol.129 (28/29), p.1581-1585

2004

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Interdisciplinary management of total knee replacement in a haemophilia patient with high-titre inhibitor and severe arthropathy complicated by an aneurysmatic bone cyst

Haemophilia : the official journal of the World Federation of Hemophilia, 2009-01, Vol.15 (1), p.377-379

2009

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Mutation in the gene coding for coagulation factor V and resistance to activated protein C: detection of the genetic mutation by oligonucleotide ligation assay using a semi-automated system

Thrombosis and haemostasis, 1996-07, Vol.76 (1), p.53-55

1996

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Prothrombin and Factor V Mutations in Women with a History of Thrombosis during Pregnancy and the Puerperium

Rotational thrombelastometry for the bedside monitoring of recombinant hirudin

Rotation thromboelastography (ROTEM) parameters are influenced by age, gender, and oral contraception

Monitoring of NOAC

The G20210A prothrombin‐gene mutation and the plasminogen activator inhibitor (PAI‐1) 5G/5G genotype are associated with early onset of severe preeclampsia

Prospective analysis after coronary-artery bypass grafting: platelet GP IIIa polymorphism (HPA-1b/PIA2) is a risk factor for bypass occlusion, myocardial infarction, and death

Polymorphism of platelet membrane glycoprotein IIIa: human platelet antigen 1b (HPA-1b/PlA2) is an inherited risk factor for premature myocardial infarction in coronary artery disease

Thrombophilia in pregnancy: venous thromboembolism, fetal loss, preeclampsia, intrauterine growth restriction

Associations between thrombophilic risk factors and determinants of atherosclerosis and inflammation in patients with non-arteritic anterior ischaemic optic neuropathy

Platelet-function analyzer closure times indicate shear stress-induced hemostatic abnormalities in patients with aortic valve stenosis and correlate with perioperative transfusion requirements

Die Bedeutung thrombophiler Risikofaktoren bei Patienten mit arteriellen Thrombosen

Thrombophile Hämostasestörung in der Schwangerschaft: Thrombose, Abort, Präeklampsie, intrauterine Wachstumsretardierung

Antithrombotic prophylaxis for women with thrombophilia and pregnancy complications

Monitoring von NOAK

The international, prospective Glanzmann Thrombasthenia Registry: treatment and outcomes in surgical intervention

Thrombophilia and gestational venous thromboembolism

Methylenetetrahydrofolate reductase gene polymorphism and glucocorticoid intake in children with ALL and aseptic osteonecrosis

Rekombinanter Faktor VIIa bei Patienten mit Plättchenfunktionsstörungen oder Thrombozytopenien

Impact of thrombophilic risk factors in patients with arterial thromboses

Genetic typing of human platelet antigen 1 (HPA‐1) by oligonucleotide ligation assay in a specific and reliable semi‐automated system

Therapy of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)

Combined von Willebrand factor deficiency and factor XII deficiency

Das erworbene von-Willebrand-Syndrom

Interdisciplinary management of total knee replacement in a haemophilia patient with high-titre inhibitor and severe arthropathy complicated by an aneurysmatic bone cyst

Mutation in the gene coding for coagulation factor V and resistance to activated protein C: detection of the genetic mutation by oligonucleotide ligation assay using a semi-automated system

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