UB Paderborn / Katalog / Suche / in CDI

1 – 13 von 13

Sortiert nach

An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro‐Asian stone‐forming belt

JIMD reports, 2020-01, Vol.51 (1), p.45-52

2020

Link zum Volltext

Verfügbarkeit prüfen

Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics Aspects

Biomedicines, 2021-07, Vol.9 (7), p.788

2021

Link zum Volltext

Verfügbarkeit prüfen

Predictors for poststroke outcomes: the Tel Aviv Brain Acute Stroke Cohort (TABASCO) study protocol

International journal of stroke, 2012-06, Vol.7 (4), p.341-347

2012

Link zum Volltext

Verfügbarkeit prüfen

Gender differences in the expression of erythrocyte aggregation in relation to B beta-fibrinogen gene polymorphisms in apparently healthy individuals

Thrombosis and haemostasis, 2006-03, Vol.95 (3), p.428

2006

Link zum Volltext

Verfügbarkeit prüfen

The Price of Stress: High Bedtime Salivary Cortisol Levels Are Associated with Brain Atrophy and Cognitive Decline in Stroke Survivors. Results from the TABASCO Prospective Cohort Study

Journal of Alzheimer's disease, 2018-01, Vol.65 (4), p.1365

2018

Link zum Volltext

Verfügbarkeit prüfen

Urine metabolomics reveals novel physiologic functions of human aldehyde oxidase and provides biomarkers for typing xanthinuria

Metabolomics, 2012-10, Vol.8 (5), p.951-959

2012

Link zum Volltext

Verfügbarkeit prüfen

Association of the -757T>C polymorphism in the CRP gene with circulating C-reactive protein levels and carotid atherosclerosis

Thrombosis research, 2009-09, Vol.124 (4), p.458-462

2009

Link zum Volltext

Verfügbarkeit prüfen

The Two Common Mutations Causing Factor XI Deficiency in Jews Stem From Distinct Founders: One of Ancient Middle Eastern Origin and Another of More Recent European Origin

Blood, 1997-10, Vol.90 (7), p.2654-2659

1997

Link zum Volltext

Verfügbarkeit prüfen

Age Estimates of Two Common Mutations Causing Factor XI Deficiency: Recent Genetic Drift Is Not Necessary for Elevated Disease Incidence among Ashkenazi Jews

American journal of human genetics, 1999-04, Vol.64 (4), p.1071-1075

1999

Link zum Volltext

Verfügbarkeit prüfen

Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene

Blood, 1995-01, Vol.85 (2), p.414-420

1995

Link zum Volltext

Verfügbarkeit prüfen

Current strategy for genetic analysis of haemophilia A families

Haemophilia : the official journal of the World Federation of Hemophilia, 1996-01, Vol.2 (1), p.11-17

1996

Link zum Volltext

Verfügbarkeit prüfen

The two common mutations causing factor XI deficiency in Jews stem from distinct founders : One of ancient middle eastern origin and another of more recent European origin

Blood, 1997-10, Vol.90 (7), p.2654-2659

1997

Link zum Volltext

Verfügbarkeit prüfen

Glanzmann's Thrombasthenia Associated With Deletion-Insertion and Alternative Splicing in the Glycoprotein IIb Gene

Blood, 1995-01, Vol.85 (2), p.414-420

1995

Link zum Volltext

Verfügbarkeit prüfen

1 – 13 von 13

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(13)
Mit Volltextzugriff
(11)

Publikationsform

Artikel
(13)

Sprache

Englisch
(13)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(9)
Science & Technology
(9)
Humans
(7)
Biological And Medical Sciences
(5)
Female
(5)
Male
(5)
Medical Sciences
(5)
Aged
(4)
Hematologic And Hematopoietic Diseases
(4)
Hematology
(4)
Platelet Diseases And Coagulopathies
(4)
Jews - Genetics
(3)
Risk Factors
(3)
Alleles
(2)
Arabs
(2)
Cardiovascular System & Cardiology
(2)
Cognition Disorders - Etiology
(2)
Factor Xi Deficiency - Genetics
(2)
Gene Frequency
(2)
Genotype
(2)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro‐Asian stone‐forming belt

Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics Aspects

Predictors for poststroke outcomes: the Tel Aviv Brain Acute Stroke Cohort (TABASCO) study protocol

Gender differences in the expression of erythrocyte aggregation in relation to B beta-fibrinogen gene polymorphisms in apparently healthy individuals

The Price of Stress: High Bedtime Salivary Cortisol Levels Are Associated with Brain Atrophy and Cognitive Decline in Stroke Survivors. Results from the TABASCO Prospective Cohort Study

Urine metabolomics reveals novel physiologic functions of human aldehyde oxidase and provides biomarkers for typing xanthinuria

Association of the -757T>C polymorphism in the CRP gene with circulating C-reactive protein levels and carotid atherosclerosis

The Two Common Mutations Causing Factor XI Deficiency in Jews Stem From Distinct Founders: One of Ancient Middle Eastern Origin and Another of More Recent European Origin

Age Estimates of Two Common Mutations Causing Factor XI Deficiency: Recent Genetic Drift Is Not Necessary for Elevated Disease Incidence among Ashkenazi Jews

Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene

Current strategy for genetic analysis of haemophilia A families

The two common mutations causing factor XI deficiency in Jews stem from distinct founders : One of ancient middle eastern origin and another of more recent European origin

Glanzmann's Thrombasthenia Associated With Deletion-Insertion and Alternative Splicing in the Glycoprotein IIb Gene

Suchergebnisse filtern