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Institut für Klinische Chemie und Laboratoriumsmedizin

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Lippi, Giuseppe; Gillery, Philippe; Kazmierczak, Steven et al.

Clinical Chemistry and Laboratory Medicine: progress and new challenges for our 50-year-old journal

CLINICAL CHEMISTRY AND LABORATORY MEDICINE. Bd. 51. H. 1. 2013 S. 5-7


Keller, Till; Ojeda, Francisco; Zeller, Tanja et al.

Defining a reference population to determine the 99th percentile of a contemporary sensitive cardiac troponin I assay

INTERNATIONAL JOURNAL OF CARDIOLOGY. Bd. 167. H. 4. 2013 S. 1423-1429


Fottner, C.; Rossmann, H.; Bickmann, J. K. et al.

Definition of a new algorithm for molecular-genetic testing of patients with hereditary pheochromocytoma and paraganglioma syndromes

EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES. Bd. 121. H. 3. 2013


Khuseyinova, N.; Schnabel, R.; Ullmann, A. et al.

Determinants of arterial stiffness in pre- and postmenopausal women

EUROPEAN HEART JOURNAL. Bd. 34. 2013 S. 314-314



Zimmermann, Anca; Grigorescu-Sido, Paula; Rossmann, Heidi et al.

Dynamic changes of lipid profile in Romanian patients with Gaucher disease type 1 under enzyme replacement therapy: a prospective study

JOURNAL OF INHERITED METABOLIC DISEASE. Bd. 36. H. 3. 2013 S. 555-563


Prinz, Nadine; Clemens, Natascha; Canisius, Antje et al.

Endosomal NADPH-oxidase is critical for induction of the tissue factor gene in monocytes and endothelial cells

THROMBOSIS AND HAEMOSTASIS. Bd. 109. H. 3. 2013 S. 525-531


Schofer, Niklas; Brunner, Fabian; Schlueter, Michael et al.

Evaluation of a Super-Sensitivity Cardiac Troponin I Assay for Diagnosing Non ST-Segment Elevation Myocardial Infarction

CIRCULATION. Bd. 128. H. 22. 2013


Trabzuni, Daniah; Ryten, Mina; Emmett, Warren et al.

Fine-Mapping, Gene Expression and Splicing Analysis of the Disease Associated LRRK2 Locus

PLOS ONE. Bd. 8. H. 8. 2013


Lukas, Jan; Giese, Anne-Katrin; Markoff, Arseni et al.

Functional Characterisation of Alpha-Galactosidase A Mutations as a Basis for a New Classification System in Fabry Disease

PLOS GENETICS. Bd. 9. H. 8. 2013