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...

Effect of Eriocalyxin B on prostatic inflammation and pelvic pain in a mouse model of experimental autoimmune prostatitis

The Prostate, 2020-12, Vol.80 (16), p.1394-1404

2020

Volltextzugriff (PDF)

CaMK4‐dependent phosphorylation of Akt/mTOR underlies Th17 excessive activation in experimental autoimmune prostatitis

The FASEB journal, 2020-10, Vol.34 (10), p.14006-14023

2020

Volltextzugriff (PDF)

Microglial activation and neurobiological alterations in experimental autoimmune prostatitis-induced depressive-like behavior in mice

Neuropsychiatric disease and treatment, 2019-08, Vol.15, p.2231-2245

2019

Volltextzugriff (PDF)

Real-world evidence of avatrombopag for the treatment of immune thrombocytopenia intolerant or ineffective to eltrombopag/hetrombopag

British journal of haematology, 2024-10

2024

Volltextzugriff (PDF)

Analysis of mechanical strengths of extreme line casing joint considering geometric, material, and contact nonlinearities

Petroleum science, 2024-06, Vol.21 (3), p.1992-2004

2024

Volltextzugriff (PDF)

Development of acquired factor V inhibitor after treatment with ceftazidime: a case report and review of the literature

Drug design, development and therapy, 2015-01, Vol.9 (default), p.2395-2398

2015

Volltextzugriff (PDF)

Clinical characteristics and outcomes of adult patients with acquired thrombotic thrombocytopenic purpura: a single center retrospective study

Annals of palliative medicine, 2021-05, Vol.10 (5), p.5351-5358

2021

Volltextzugriff (PDF)

Valproic acid-associated low fibrinogen and delayed intracranial hemorrhage: case report and mini literature review

Drug design, development and therapy, 2013-01, Vol.7 (default), p.767-770

2013

Volltextzugriff (PDF)

Clinical, Pathological, and Genetic Analysis of Ten Patients with MYH9-Related Disease

Acta haematologica, 2013-01, Vol.129 (2), p.106-113

2013

Volltextzugriff (PDF)

Molecular mechanisms of antithrombin gene mutations in 3 pedigrees with hereditary antithrombin deficiency

Zhōnghuá xuèyèxué zázhì, 2013-03, Vol.34 (3), p.253-255

2013

Volltextzugriff (PDF)

Gene analysis and pathogenesis in 40 patients with hemophilia B

Zhongguo shi yan xue ye xue za zhi, 2013-08, Vol.21 (4), p.963

2013

Volltextzugriff (PDF)

Clinical study of thalidomide combined with dexamethasone for the treatment of elderly patients with newly diagnosed multiple myeloma

Asian Pacific journal of cancer prevention : APJCP, 2012-01, Vol.13 (9), p.4777-4781

2012

Volltextzugriff (PDF)

Detection of alloantibodies against Factor VIII in plasma of patients with hemophilia A and its relationship with Factor VIIIC domain

Zhongguo shi yan xue ye xue za zhi, 2013-10, Vol.21 (5), p.1211

2013

Volltextzugriff (PDF)

Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene

Zhōnghuá xuèyèxué zázhì, 2013-09, Vol.34 (9), p.751-756

2013

Volltextzugriff (PDF)

Prenatal diagnosis for two families of congenital factor V deficiency

Zhonghua yi xue yi chuan xue za zhi, 2011-12, Vol.28 (6), p.679

2011

Volltextzugriff (PDF)

Analysis of coagulation factor VIII inhibitor development related factors in hemophilia A patients.

Zhōnghuá xuèyèxué zázhì, 2010-03, Vol.31 (3), p.168-171

2010

Volltextzugriff (PDF)

Clinical features and gene analyses of six patients with MYH9-related disease

Zhōnghuá xuèyèxué zázhì, 2012-07, Vol.33 (7), p.552-555

2012

Volltextzugriff (PDF)

Relationship between factor VIII inhibitor development and polymorphisms of TNFα and CTLA-4 gene in Chinese Han patients with hemophilia A

Zhōnghuá xuèyèxué zázhì, 2011-03, Vol.32 (3), p.168-172

2011

Volltextzugriff (PDF)

Genotype and phenotype analysis of congenital coagulator factor VII deficiency in four Chinese pedigrees

Zhōnghuá xuèyèxué zázhì, 2011-03, Vol.32 (3), p.147-152

2011

Volltextzugriff (PDF)

Improving the diagnosis and treatment in thrombotic diseases

Chung-hua nei kʿo tsa chih, 2007-11, Vol.46 (11), p.889

2007

Volltextzugriff (PDF)

Alteration and biological significance of peripheral dendritic cells in patients with chronic idiopathic thrombocytopenic purpura

Zhōnghuá xuèyèxué zázhì, 2008-03, Vol.29 (3), p.187-191

2008

Volltextzugriff (PDF)

Pathology, diagnosis and treatment of a patient with hemotidrosis.

Zhōnghuá xuèyèxué zázhì, 2010-03, Vol.31 (3), p.157-160

2010

Volltextzugriff (PDF)

Inherited dysfibrinogenemia caused by Arg16His mutation in alpha chain of fibrinogen.

Zhōnghuá xuèyèxué zázhì, 2010-03, Vol.31 (3), p.154-156

2010

Volltextzugriff (PDF)

Alterations of CD4+ CD25+ regulatory T cells in patients with idiopathic thrombocytopenic purpura

Zhōnghuá xuèyèxué zázhì, 2007-03, Vol.28 (3), p.184-188

2007

Volltextzugriff (PDF)

Gene analysis of five inherited factor V deficiency cases

Zhōnghuá xuèyèxué zázhì, 2008-03, Vol.29 (3), p.145-148

2008

Volltextzugriff (PDF)

1 – 25 von 549

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(385)
Mit Volltextzugriff
(475)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(280)
Life Sciences & Biomedicine
(124)
Physical Sciences
(122)
Humans
(81)
Technology
(80)
Chemistry
(65)
Male
(55)
Engineering
(52)
Physics
(47)
Female
(46)
Adult
(38)
Middle Aged
(36)
Materials Science
(34)
Animals
(29)
Materials Science, Multidisciplinary
(26)
Chemistry, Multidisciplinary
(22)
Aged
(20)
Adolescent
(18)
Exact Sciences And Technology
(17)
Physics, Applied
(17)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Effect of Eriocalyxin B on prostatic inflammation and pelvic pain in a mouse model of experimental autoimmune prostatitis

CaMK4‐dependent phosphorylation of Akt/mTOR underlies Th17 excessive activation in experimental autoimmune prostatitis

Microglial activation and neurobiological alterations in experimental autoimmune prostatitis-induced depressive-like behavior in mice

Real-world evidence of avatrombopag for the treatment of immune thrombocytopenia intolerant or ineffective to eltrombopag/hetrombopag

Analysis of mechanical strengths of extreme line casing joint considering geometric, material, and contact nonlinearities

Development of acquired factor V inhibitor after treatment with ceftazidime: a case report and review of the literature

Clinical characteristics and outcomes of adult patients with acquired thrombotic thrombocytopenic purpura: a single center retrospective study

Valproic acid-associated low fibrinogen and delayed intracranial hemorrhage: case report and mini literature review

Clinical, Pathological, and Genetic Analysis of Ten Patients with MYH9-Related Disease

Molecular mechanisms of antithrombin gene mutations in 3 pedigrees with hereditary antithrombin deficiency

Gene analysis and pathogenesis in 40 patients with hemophilia B

Clinical study of thalidomide combined with dexamethasone for the treatment of elderly patients with newly diagnosed multiple myeloma

Detection of alloantibodies against Factor VIII in plasma of patients with hemophilia A and its relationship with Factor VIIIC domain

Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene

Prenatal diagnosis for two families of congenital factor V deficiency

Analysis of coagulation factor VIII inhibitor development related factors in hemophilia A patients.

Clinical features and gene analyses of six patients with MYH9-related disease

Relationship between factor VIII inhibitor development and polymorphisms of TNFα and CTLA-4 gene in Chinese Han patients with hemophilia A

Genotype and phenotype analysis of congenital coagulator factor VII deficiency in four Chinese pedigrees

Improving the diagnosis and treatment in thrombotic diseases

Alteration and biological significance of peripheral dendritic cells in patients with chronic idiopathic thrombocytopenic purpura

Pathology, diagnosis and treatment of a patient with hemotidrosis.

Inherited dysfibrinogenemia caused by Arg16His mutation in alpha chain of fibrinogen.

Alterations of CD4+ CD25+ regulatory T cells in patients with idiopathic thrombocytopenic purpura

Gene analysis of five inherited factor V deficiency cases

Suchergebnisse filtern