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Zentrum für translationale vaskuläre Biologie (CTVB)

Forschungsschwerpunkt / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Tzikas, S.; Palapies, L.; Zeller, T. et al.

GDF-15 is a predictor of cardiovascular events in patients presenting with suspicion of acute coronary syndrome

EUROPEAN HEART JOURNAL. Bd. 36. 2015 S. 689-690


Panova-Noeva, M.; Grossmann, V; Hermanns, I et al.

Genetic and non-genetic determinants of MPV differ in males and females - results from the Gutenberg Health Study

JOURNAL OF THROMBOSIS AND HAEMOSTASIS. Bd. 13. 2015 S. 924-925


Alidjanov, J. F.; Pilatz, A.; Abdufattaev, U. A. et al.

German validation of the Acute Cystitis Symptom Score

UROLOGE. Bd. 54. H. 9. 2015 S. 1269-1276


Steven, S.; Kopp, M.; Mikhed, Y. et al.

Glucagon-like peptide 1 (GLP1) improves disseminated intravasal coagulation (DIC) and vascular function in LPS-induced endotoxemia

EUROPEAN HEART JOURNAL. Bd. 36. 2015 S. 437-438


Breuckmann, Frank; Hochadel, Matthias; Darius, Harald et al.

Guideline-adherence and perspectives in the acute management of unstable angina - Initial results from the German chest pain unit registry

JOURNAL OF CARDIOLOGY. Bd. 66. H. 1-2. 2015 S. 108-113


Keller, Karsten; Beule, Johannes; Coldewey, Meike et al.

Heart rate in pulmonary embolism

INTERNAL AND EMERGENCY MEDICINE. Bd. 10. H. 6. 2015 S. 663-669


Hinkel, Rabea; Lange, Philipp; Petersen, Bjoern et al.

Heme Oxygenase-1 Gene Therapy Provides Cardioprotection Via Control of Post-Ischemic Inflammation An Experimental Study in a Pre-Clinical Pig Model

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY. Bd. 66. H. 2. 2015 S. 154-165


Wenzel, Philip; Rossmann, Heidi; Mueller, Christian et al.

Heme oxygenase-1 suppresses a pro-inflammatory phenotype in monocytes and determines endothelial function and arterial hypertension in mice and humans

EUROPEAN HEART JOURNAL. Bd. 36. H. 48. 2015 S. 3437-3446



Bork, K.; Wulff, K.; Witzke, G. et al.

Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations

ALLERGY. Bd. 70. H. 8. 2015 S. 1004-1012