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...

Identification of novel FLT‐3 Asp835 mutations in adult acute myeloid leukaemia

British journal of haematology, 2001-06, Vol.113 (4), p.983-988

2001

Volltextzugriff (PDF)

FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group

British journal of haematology, 2000-10, Vol.111 (1), p.190-195

2000

Volltextzugriff (PDF)

Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD

Thrombosis research, 2010-09, Vol.126 (3), p.227-231

2010

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)

Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-05, Vol.10 (3), p.218-231

2004

Volltextzugriff (PDF)

The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-05, Vol.10 (3), p.199-217

2004

Volltextzugriff (PDF)

HLA Class II Profile: A Weak Determinant of Factor VIII Inhibitor Development in Severe Haemophilia A

Thrombosis and haemostasis, 1997, Vol.77 (2), p.234-237

1997

Volltextzugriff (PDF)

Precise carrier diagnosis in families with haemophilia A: use of conformation sensitive gel electrophoresis for mutation screening and polymorphism analysis

Thrombosis and haemostasis, 1998-04, Vol.79 (4), p.723-726

1998

Volltextzugriff (PDF)

Factor VIII Inhibitors in Mild and Moderate-severity Haemophilia A

Thrombosis and haemostasis, 1998, Vol.79 (4), p.762-766

1998

Volltextzugriff (PDF)

Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S

Blood, 2000-03, Vol.95 (6), p.1935-1941

2000

Volltextzugriff (PDF)

Genetic testing for von Willebrand disease: the case for

Journal of thrombosis and haemostasis, 2010-01, Vol.8 (1), p.13-16

2010

Volltextzugriff (PDF)

Antithrombins Wibble and Wobble (T85M/K) : Archetypal conformational diseases with in vivo latent-transition, thrombosis, and heparin activation

Blood, 1998-10, Vol.92 (8), p.2696-2706

1998

Volltextzugriff (PDF)

Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia

Thrombosis and haemostasis, 1997-12, Vol.78 (6), p.1426-1429

1997

Volltextzugriff (PDF)

In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-09, Vol.22 (5), p.e484-e487

2016

Volltextzugriff (PDF)

Genomic structure of human FLT3: implications for mutational analysis

British journal of haematology, 2001-06, Vol.113 (4), p.1076-1077

2001

Volltextzugriff (PDF)

A framework for genetic service provision for haemophilia and other inherited bleeding disorders

Haemophilia : the official journal of the World Federation of Hemophilia, 2005-03, Vol.11 (2), p.145-163

2005

Volltextzugriff (PDF)

Major structural defects in the antithrombin gene in four families with type I antithrombin deficiency--partial/complete deletions and rearrangement of the antithrombin gene

Thrombosis and haemostasis, 2000-05, Vol.83 (5), p.715-721

2000

Volltextzugriff (PDF)

A rapid method for haemophilia B mutation detection using conformation sensitive gel electrophoresis

British journal of haematology, 1999-03, Vol.104 (4), p.915-918

1999

Volltextzugriff (PDF)

Are aberrant BCR-ABL transcripts more common than previously thought?

British journal of haematology, 2000-12, Vol.111 (4), p.1109-1111

2000

Volltextzugriff (PDF)

Two novel type 2N von Willebrand disease–causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor

Blood, 2000-03, Vol.95 (6), p.2000-2007

2000

Volltextzugriff (PDF)

High prevalence of a mutation in the factor V gene within the U.K. population: relationship to activated protein C resistance and familial thrombosis

British journal of haematology, 1994-09, Vol.88 (1), p.219-222

1994

Volltextzugriff (PDF)

Mutations in PTPN11 are uncommon in adult myelodysplastic syndromes and acute myeloid leukaemia

British journal of haematology, 2004-03, Vol.124 (6), p.843-844

2004

Volltextzugriff (PDF)

Influence of the −675 4G/5G dimorphism of the plasminogen activator inhibitor 1 promoter on thrombotic risk in patients with factor V Leiden

British journal of haematology, 2000-07, Vol.110 (1), p.135-138

2000

Volltextzugriff (PDF)

Factor VIII gene rearrangements in patients with severe haemophilia A

The Lancet (British edition), 1994-02, Vol.343 (8893), p.329-330

1994

Volltextzugriff (PDF)

Assembly of multimeric von Willebrand factor directs sorting of P-selectin

Arteriosclerosis, thrombosis, and vascular biology, 2000-07, Vol.20 (7), p.1763-1768

2000

Volltextzugriff (PDF)

1 – 25 von 1.086

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(892)
Mit Volltextzugriff
(825)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(1.082)
Deutsch
(2)
Russisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(581)
Life Sciences & Biomedicine
(489)
Humans
(433)
Male
(231)
Female
(209)
Biological And Medical Sciences
(197)
Medical Sciences
(155)
Adult
(138)
Middle Aged
(122)
Hematology
(94)
Aged
(91)
Animals
(83)
General & Internal Medicine
(83)
Physical Sciences
(80)
Technology
(60)
Adolescent
(53)
Medicine, General & Internal
(52)
Hematologic And Hematopoietic Diseases
(51)
Oncology
(49)
Respiratory System
(49)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

British Journal Of Haematology
(45)
Blood
(32)
The Lancet
(32)
Thorax
(24)
Thrombosis And Haemostasis
(24)
Journal Of Thoracic Oncology
(22)
Bentley's Miscellany, 1837-1868
(20)
Lung Cancer
(19)
Gut
(18)
The New England Journal Of Medicine
(12)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Identification of novel FLT‐3 Asp835 mutations in adult acute myeloid leukaemia

FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group

Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD

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

Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization

The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization

HLA Class II Profile: A Weak Determinant of Factor VIII Inhibitor Development in Severe Haemophilia A

Precise carrier diagnosis in families with haemophilia A: use of conformation sensitive gel electrophoresis for mutation screening and polymorphism analysis

Factor VIII Inhibitors in Mild and Moderate-severity Haemophilia A

Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S

Genetic testing for von Willebrand disease: the case for

Antithrombins Wibble and Wobble (T85M/K) : Archetypal conformational diseases with in vivo latent-transition, thrombosis, and heparin activation

Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia

In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion

Genomic structure of human FLT3: implications for mutational analysis

A framework for genetic service provision for haemophilia and other inherited bleeding disorders

Major structural defects in the antithrombin gene in four families with type I antithrombin deficiency--partial/complete deletions and rearrangement of the antithrombin gene

A rapid method for haemophilia B mutation detection using conformation sensitive gel electrophoresis

Are aberrant BCR-ABL transcripts more common than previously thought?

Two novel type 2N von Willebrand disease–causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor

High prevalence of a mutation in the factor V gene within the U.K. population: relationship to activated protein C resistance and familial thrombosis

Mutations in PTPN11 are uncommon in adult myelodysplastic syndromes and acute myeloid leukaemia

Influence of the −675 4G/5G dimorphism of the plasminogen activator inhibitor 1 promoter on thrombotic risk in patients with factor V Leiden

Factor VIII gene rearrangements in patients with severe haemophilia A

Assembly of multimeric von Willebrand factor directs sorting of P-selectin

Suchergebnisse filtern