UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 406

Sortiert nach

von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein

Journal of thrombosis and haemostasis, 2011-07, Vol.9, p.209-215

2011

Volltextzugriff (PDF)

Acquired von Willebrand syndrome in congenital heart disease surgery: results from an observational case‐series

Journal of thrombosis and haemostasis, 2018-11, Vol.16 (11), p.2150-2158

2018

Volltextzugriff (PDF)

Deep intronic ‘mutations’ cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNA

Journal of thrombosis and haemostasis, 2013-09, Vol.11 (9), p.1679-1687

2013

Volltextzugriff (PDF)

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

Journal of thrombosis and haemostasis, 2006-10, Vol.4 (10), p.2103-2114

2006

Volltextzugriff (PDF)

Prospective evaluation of a pediatric bleeding questionnaire and the ISTH bleeding assessment tool in children and parents in routine clinical practice

Journal of thrombosis and haemostasis, 2012-07, Vol.10 (7), p.1335-1341

2012

Volltextzugriff (PDF)

A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD)

Journal of thrombosis and haemostasis, 2006-04, Vol.4 (4), p.766-773

2006

Volltextzugriff (PDF)

Shear‐induced unfolding activates von Willebrand factor A2 domain for proteolysis

Journal of thrombosis and haemostasis, 2009-12, Vol.7 (12), p.2096-2105

2009

Volltextzugriff (PDF)

Clopidogrel Resistance in Neurovascular Stenting: Correlations between Light Transmission Aggregometry, VerifyNow, and the Multiplate

American journal of neuroradiology : AJNR, 2015-10, Vol.36 (10), p.1953-1958

2015

Volltextzugriff (PDF)

Diagnosis of von Willebrand disease subtypes: implications for treatment

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-11, Vol.14 (s5), p.27-38

BUDDE, U.

2008

Volltextzugriff (PDF)

Diagnostic workup of patients with acquired von Willebrand syndrome: a retrospective single‐centre cohort study

Journal of thrombosis and haemostasis, 2008-04, Vol.6 (4), p.569-576

2008

Volltextzugriff (PDF)

Ex vivo human placental transfer study on recombinant Von Willebrand factor (rVWF)

Placenta (Eastbourne), 2021-08, Vol.111, p.69-75

2021

Volltextzugriff (PDF)

Identification and characterization of the elusive mutation causing the historical von Willebrand Disease type IIC Miami

Journal of thrombosis and haemostasis, 2016-09, Vol.14 (9), p.1725-1735

2016

Volltextzugriff (PDF)

An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS‐VWF study

Journal of thrombosis and haemostasis, 2018-08, Vol.16 (8), p.1604-1613

2018

Volltextzugriff (PDF)

Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM‐1VWD)

Journal of thrombosis and haemostasis, 2008-05, Vol.6 (5), p.762-771

2008

Volltextzugriff (PDF)

Inflammation-associated ADAMTS13 deficiency promotes formation of ultra-large von Willebrand factor

Haematologica (Roma), 2008-01, Vol.93 (1), p.137-140

2008

Volltextzugriff (PDF)

P-045: Dead fetus syndrome (DFS) in a high risk twin pregnancy – is laboratory testing for DIC useful?

Thrombosis research, 2017-03, Vol.151, p.S123-S124

2017

Volltextzugriff (PDF)

Lupus anticoagulants associated inhibitor against factor IX in a young patient with haemophilia B

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-09, Vol.22 (5), p.e437-e439

2016

Volltextzugriff (PDF)

Clopidogrel Resistance in Neurovascular Stenting: Correlations between Light Transmission Aggregometry, VerifyNow, and the Multiplate

American journal of neuroradiology : AJNR, 2015-10, Vol.36 (10), p.1953-1958

2015

Volltextzugriff (PDF)

Loss of high-molecular-weight von Willebrand factor multimers mainly affects platelet aggregation in patients with aortic stenosis

Thrombosis and haemostasis, 2010-02, Vol.103 (2), p.408

2010

Volltextzugriff (PDF)

In vivo von Willebrand factor size heterogeneity in spite of the clinical deficiency of ADAMTS‐13

Journal of thrombosis and haemostasis, 2011-12, Vol.9 (12), p.2506-2508

2011

Volltextzugriff (PDF)

Acquired type 2A von Willebrand syndrome caused by aortic valve disease corrects during valve surgery

British journal of anaesthesia : BJA, 2011-04, Vol.106 (4), p.494-500

2011

Volltextzugriff (PDF)

Epidemiology and general guidelines of the management of acquired haemophilia and von Willebrand syndrome

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-07, Vol.14 (s3), p.49-55

2008

Volltextzugriff (PDF)

Large deletions identified in patients with von Willebrand disease using multiple ligation‐dependent probe amplification

Journal of thrombosis and haemostasis, 2011-05, Vol.9 (5), p.1083-1086

2011

Volltextzugriff (PDF)

Germline de novo mutations and linkage markers vs. DNA sequencing for carrier detection in von Willebrand disease

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-07, Vol.20 (4), p.e311-e317

2014

Volltextzugriff (PDF)

Interactions of von Willebrand factor and ADAMTS13 in von Willebrand disease and thrombotic thrombocytopenic purpura

Hämostaseologie, 2014, Vol.34 (3), p.215

2014

Volltextzugriff (PDF)

1 – 25 von 406

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(339)
Mit Volltextzugriff
(317)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(334)
Deutsch
(81)
Japanisch
(56)
Russisch
(1)

Erscheinungsjahr

n.n

Thema

Humans
(229)
Science & Technology
(227)
Life Sciences & Biomedicine
(208)
Male
(127)
Female
(120)
Hematology
(103)
Adult
(84)
Biological And Medical Sciences
(84)
Medical Sciences
(77)
Middle Aged
(66)
Cardiovascular System & Cardiology
(63)
Adolescent
(50)
Peripheral Vascular Disease
(49)
Aged
(47)
Child
(44)
Hematologic And Hematopoietic Diseases
(40)
Von Willebrand Factor
(40)
Von Willebrand Factor - Genetics
(35)
Platelet Diseases And Coagulopathies
(33)
Von Willebrand Factor - Metabolism
(33)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein

Acquired von Willebrand syndrome in congenital heart disease surgery: results from an observational case‐series

Deep intronic ‘mutations’ cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNA

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

Prospective evaluation of a pediatric bleeding questionnaire and the ISTH bleeding assessment tool in children and parents in routine clinical practice

A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD)

Shear‐induced unfolding activates von Willebrand factor A2 domain for proteolysis

Clopidogrel Resistance in Neurovascular Stenting: Correlations between Light Transmission Aggregometry, VerifyNow, and the Multiplate

Diagnosis of von Willebrand disease subtypes: implications for treatment

Diagnostic workup of patients with acquired von Willebrand syndrome: a retrospective single‐centre cohort study

Ex vivo human placental transfer study on recombinant Von Willebrand factor (rVWF)

Identification and characterization of the elusive mutation causing the historical von Willebrand Disease type IIC Miami

An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS‐VWF study

Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM‐1VWD)

Inflammation-associated ADAMTS13 deficiency promotes formation of ultra-large von Willebrand factor

P-045: Dead fetus syndrome (DFS) in a high risk twin pregnancy – is laboratory testing for DIC useful?

Lupus anticoagulants associated inhibitor against factor IX in a young patient with haemophilia B

Clopidogrel Resistance in Neurovascular Stenting: Correlations between Light Transmission Aggregometry, VerifyNow, and the Multiplate

Loss of high-molecular-weight von Willebrand factor multimers mainly affects platelet aggregation in patients with aortic stenosis

In vivo von Willebrand factor size heterogeneity in spite of the clinical deficiency of ADAMTS‐13

Acquired type 2A von Willebrand syndrome caused by aortic valve disease corrects during valve surgery

Epidemiology and general guidelines of the management of acquired haemophilia and von Willebrand syndrome

Large deletions identified in patients with von Willebrand disease using multiple ligation‐dependent probe amplification

Germline de novo mutations and linkage markers vs. DNA sequencing for carrier detection in von Willebrand disease

Interactions of von Willebrand factor and ADAMTS13 in von Willebrand disease and thrombotic thrombocytopenic purpura

Suchergebnisse filtern