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...

How I treat the acquired von Willebrand syndrome

Blood, 2011-06, Vol.117 (25), p.6777-6785

2011

Volltextzugriff (PDF)

Activation-independent platelet adhesion and aggregation under elevated shear stress

Blood, 2006-09, Vol.108 (6), p.1903-1910

2006

Volltextzugriff (PDF)

An intact PDZ motif is essential for correct P2Y12 purinoceptor traffic in human platelets

Blood, 2011-11, Vol.118 (20), p.5641-5651

2011

Volltextzugriff (PDF)

Von Willebrand disease and other bleeding disorders in women: consensus on diagnosis and management from an international expert panel

American journal of obstetrics and gynecology, 2009-07, Vol.201 (1), p.12.e1-12.e8

2009

Volltextzugriff (PDF)

The impact of bleeding history, von Willebrand factor and PFA–100® on the diagnosis of type 1 von Willebrand disease: results from the European study MCMDM‐1VWD

British journal of haematology, 2010-11, Vol.151 (3), p.245-251

2010

Volltextzugriff (PDF)

Clinical use of Haemate(R) P in inherited von Willebrand's disease: a cohort study on 100 Italian patients

Haematologica (Roma), 2007-07, Vol.92 (7), p.944-951

2007

Volltextzugriff (PDF)

Evaluation and management of postpartum hemorrhage: consensus from an international expert panel

Transfusion, 2014-07, Vol.54 (7), p.1756-1768

2014

Volltextzugriff (PDF)

An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees

Blood, 2004-10, Vol.104 (8), p.2359-2367

2004

Volltextzugriff (PDF)

Bleeding tendency and efficacy of anti-haemorrhagic treatments in patients with type 1 von Willebrand disease and increased von Willebrand factor clearance

Thrombosis and haemostasis, 2011-04, Vol.105 (4), p.647-654

2011

Volltextzugriff (PDF)

Classification of inherited von Willebrand disease and implications in clinical practice

Thrombosis research, 2009-11, Vol.124, p.S2-S6

Federici, Augusto B

2009

Volltextzugriff (PDF)

Platelet morphological changes in 2 patients with von Willebrand disease type 3 caused by large homozygous deletions of the von Willebrand factor gene

Haematologica (Roma), 2009-11, Vol.94 (11), p.1627-1629

2009

Volltextzugriff (PDF)

Evaluation and management of acute menorrhagia in women with and without underlying bleeding disorders: consensus from an international expert panel

European journal of obstetrics & gynecology and reproductive biology, 2011-10, Vol.158 (2), p.124-134

2011

Volltextzugriff (PDF)

Acquired von Willebrand Syndrome: An Underdiagnosed and Misdiagnosed Bleeding Complication in Patients With Lymphoproliferative and Myeloproliferative Disorders

Seminars in hematology, 2006, Vol.43 (1), p.S48-S58

Federici, Augusto B.

2006

Volltextzugriff (PDF)

Abnormal VWF modifies megakaryocytopoiesis: studies of platelets and megakaryocyte cultures from patients with von Willebrand disease type 2B

Blood, 2010-04, Vol.115 (13), p.2649-2656

2010

Volltextzugriff (PDF)

Von Willebrand's disease in the year 2003: towards the complete identification of gene defects for correct diagnosis and treatment

Haematologica (Roma), 2003-01, Vol.88 (1), p.94

2003

Volltextzugriff (PDF)

Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European study

Blood, 2004-03, Vol.103 (6), p.2032-2038

2004

Volltextzugriff (PDF)

Management of inherited von Willebrand disease in 2007

Annals of medicine (Helsinki), 2007, Vol.39 (5), p.346-358

2007

Volltextzugriff (PDF)

Circulating and progenitor endothelial cells are abnormal in patients with different types of von Willebrand disease and correlate with markers of angiogenesis

American journal of hematology, 2011-08, Vol.86 (8), p.650-656

2011

Volltextzugriff (PDF)

Evaluation of the PFA-100 system in the diagnosis and therapeutic monitoring of patients with von Willebrand disease

Thrombosis and haemostasis, 1999-07, Vol.82 (1), p.35-39

1999

Volltextzugriff (PDF)

Molecular characterization, recombinant protein expression, and mRNA analysis of type 3 von Willebrand disease: Studies of an Italian cohort of 10 patients

American journal of hematology, 2012-09, Vol.87 (9), p.870-874

2012

Volltextzugriff (PDF)

Acquired von Willebrand syndrome type 2A in a JAK2-positive essential thrombocythaemia-affected member of a large von Willebrand disease family with a novel autosomal dominant A1716P mutation

Thrombosis and haemostasis, 2011-05, Vol.105 (5), p.921-924

2011

Volltextzugriff (PDF)

Von Willebrand factor and fibrinolytic parameters during the desmopressin test in patients with Cushing's disease

British journal of clinical pharmacology, 2011-01, Vol.71 (1), p.132-136

2011

Volltextzugriff (PDF)

Diagnosis and management of inherited von Willebrand disease in the next decade: panel discussion

Thrombosis research, 2009-11, Vol.124, p.S20-S21

2009

Volltextzugriff (PDF)

1 – 25 von 56

Suche als RSS-Feed

Aktive Filter

ThemaMedical Sciences

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(54)
Mit Volltextzugriff
(43)

Publikationsform

Artikel
(56)

Sprache

Englisch
(56)

Erscheinungsjahr

n.n

Thema

Biological And Medical Sciences
(56)
Humans
(50)
Hematologic And Hematopoietic Diseases
(43)
Life Sciences & Biomedicine
(37)
Science & Technology
(37)
Platelet Diseases And Coagulopathies
(36)
Hematology
(31)
Female
(24)
Male
(22)
Adult
(18)
Middle Aged
(16)
Von Willebrand Factor
(16)
Aged
(13)
Von Willebrand Diseases - Genetics
(13)
Adolescent
(12)
Von Willebrand Disease
(12)
Von Willebrand Factor - Genetics
(12)
Von Willebrand Factor - Metabolism
(12)
Child
(10)

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

How I treat the acquired von Willebrand syndrome

Activation-independent platelet adhesion and aggregation under elevated shear stress

An intact PDZ motif is essential for correct P2Y12 purinoceptor traffic in human platelets

Von Willebrand disease and other bleeding disorders in women: consensus on diagnosis and management from an international expert panel

The impact of bleeding history, von Willebrand factor and PFA–100® on the diagnosis of type 1 von Willebrand disease: results from the European study MCMDM‐1VWD

Clinical use of Haemate(R) P in inherited von Willebrand's disease: a cohort study on 100 Italian patients

Evaluation and management of postpartum hemorrhage: consensus from an international expert panel

An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees

Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD

Bleeding tendency and efficacy of anti-haemorrhagic treatments in patients with type 1 von Willebrand disease and increased von Willebrand factor clearance

Classification of inherited von Willebrand disease and implications in clinical practice

Platelet morphological changes in 2 patients with von Willebrand disease type 3 caused by large homozygous deletions of the von Willebrand factor gene

Evaluation and management of acute menorrhagia in women with and without underlying bleeding disorders: consensus from an international expert panel

Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: Molecular and Clinical Markers for the Diagnosis and Management of Type 1 VWD (MCMDM-1VWD)

Acquired von Willebrand Syndrome: An Underdiagnosed and Misdiagnosed Bleeding Complication in Patients With Lymphoproliferative and Myeloproliferative Disorders

Abnormal VWF modifies megakaryocytopoiesis: studies of platelets and megakaryocyte cultures from patients with von Willebrand disease type 2B

Von Willebrand's disease in the year 2003: towards the complete identification of gene defects for correct diagnosis and treatment

Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European study

Management of inherited von Willebrand disease in 2007

Circulating and progenitor endothelial cells are abnormal in patients with different types of von Willebrand disease and correlate with markers of angiogenesis

Evaluation of the PFA-100 system in the diagnosis and therapeutic monitoring of patients with von Willebrand disease

Molecular characterization, recombinant protein expression, and mRNA analysis of type 3 von Willebrand disease: Studies of an Italian cohort of 10 patients

Acquired von Willebrand syndrome type 2A in a JAK2-positive essential thrombocythaemia-affected member of a large von Willebrand disease family with a novel autosomal dominant A1716P mutation

Von Willebrand factor and fibrinolytic parameters during the desmopressin test in patients with Cushing's disease

Diagnosis and management of inherited von Willebrand disease in the next decade: panel discussion

Aktive Filter

Suchergebnisse filtern