UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

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)

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)

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)

Platelet‐dependent von Willebrand factor activity. Nomenclature and methodology: communication from the SSC of the ISTH

Journal of thrombosis and haemostasis, 2015-07, Vol.13 (7), p.1345-1350

2015

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)

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)

High-dose chemotherapy (HDCT) with auto-SCT in children with atypical teratoid/rhabdoid tumors (AT/RT): a report from the European Rhabdoid Registry (EU-RHAB)

Bone marrow transplantation (Basingstoke), 2014-03, Vol.49 (3), p.370-375

2014

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)

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)

Phenotypic and genotypic characterization of 10 Finnish patients with von Willebrand disease type 3: discovery of two main mutations

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-11, Vol.19 (6), p.e344-e348

2013

Volltextzugriff (PDF)

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

Hämostaseologie, 2014, Vol.34 (3), p.215-225

2014

Volltextzugriff (PDF)

Glial papillary tumour of the spinal cord with SMARCB1/INI1‐loss and favourable long‐term outcome

Neuropathology and applied neurobiology, 2018-02, Vol.44 (2), p.229-232

2018

Volltextzugriff (PDF)

Laboratory diagnosis of von Willebrand disease

Hämostaseologie, 2010-11, Vol.30 (4), p.203-206

2010

Volltextzugriff (PDF)

Delayed Diagnosis of Platelet-type von Willebrand Disease in a 72-year-old Lady

Klinische Padiatrie, 2015-05, Vol.227 (3), p.171

2015

Volltextzugriff (PDF)

Identification of novel NOTCH1 mutations: Increasing our knowledge of the NOTCH signaling pathway

Pediatric blood & cancer, 2014-05, Vol.61 (5), p.788-796

2014

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)

Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patient

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-07, Vol.19 (4), p.e261-e264

2013

Volltextzugriff (PDF)

Platelet-type von Willebrand Disease: Diagnostic Challenges. Flaws and Pitfalls Experienced in the THROMKID Quality Project

Klinische Padiatrie, 2015-05, Vol.227 (3), p.131-136

2015

Volltextzugriff (PDF)

Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry

Hämostaseologie, 2013, Vol.33 (2), p.138-143

2013

Volltextzugriff (PDF)

Feasibility of intensive multimodal therapy in infants affected by rhabdoid tumors - experience of the EU-RHAB registry

Klinische Padiatrie, 2014-05, Vol.226 (3), p.143-148

2014

Volltextzugriff (PDF)

An Alu‐mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary

Journal of thrombosis and haemostasis, 2008-10, Vol.6 (10), p.1729-1735

2008

Volltextzugriff (PDF)

A common 253‐kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3

Journal of thrombosis and haemostasis, 2007-04, Vol.5 (4), p.722-728

2007

Volltextzugriff (PDF)

Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD

Journal of thrombosis and haemostasis, 2006-04, Vol.4 (4), p.774-782

2006

Volltextzugriff (PDF)

Reduced von Willebrand factor secretion is associated with loss of Weibel–Palade body formation

Journal of thrombosis and haemostasis, 2012-05, Vol.10 (5), p.951-958

2012

Volltextzugriff (PDF)

Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype

Journal of thrombosis and haemostasis, 2010-09, Vol.8 (9), p.2011-2016

2010

Volltextzugriff (PDF)

1 – 25 von 149

Suche als RSS-Feed

Aktive Filter

ThemaHumans

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(146)
Mit Volltextzugriff
(107)

Publikationsform

Artikel
(149)

Sprache

Englisch
(138)
Deutsch
(12)

Erscheinungsjahr

n.n

Thema

Science & Technology
(122)
Life Sciences & Biomedicine
(120)
Male
(73)
Hematology
(72)
Female
(62)
Biological And Medical Sciences
(58)
Medical Sciences
(54)
Child
(49)
Von Willebrand Factor - Genetics
(41)
Mutation
(37)
Child, Preschool
(36)
Von Willebrand Diseases - Genetics
(35)
Adult
(34)
Cardiovascular System & Cardiology
(33)
Peripheral Vascular Disease
(32)
Phenotype
(32)
Adolescent
(31)
Hematologic And Hematopoietic Diseases
(31)
Infant
(29)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

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

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

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

Platelet‐dependent von Willebrand factor activity. Nomenclature and methodology: communication from the SSC of the ISTH

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

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

High-dose chemotherapy (HDCT) with auto-SCT in children with atypical teratoid/rhabdoid tumors (AT/RT): a report from the European Rhabdoid Registry (EU-RHAB)

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

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)

Phenotypic and genotypic characterization of 10 Finnish patients with von Willebrand disease type 3: discovery of two main mutations

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

Glial papillary tumour of the spinal cord with SMARCB1/INI1‐loss and favourable long‐term outcome

Laboratory diagnosis of von Willebrand disease

Delayed Diagnosis of Platelet-type von Willebrand Disease in a 72-year-old Lady

Identification of novel NOTCH1 mutations: Increasing our knowledge of the NOTCH signaling pathway

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

Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patient

Platelet-type von Willebrand Disease: Diagnostic Challenges. Flaws and Pitfalls Experienced in the THROMKID Quality Project

Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry

Feasibility of intensive multimodal therapy in infants affected by rhabdoid tumors - experience of the EU-RHAB registry

An Alu‐mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary

A common 253‐kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3

Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD

Reduced von Willebrand factor secretion is associated with loss of Weibel–Palade body formation

Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype

Aktive Filter

Suchergebnisse filtern