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Arteriosclerosis, Thrombosis, and Vascular Biology|October 16, 1999
Systemic inflammatory parameters in patients with atherosclerosis of the coronary and peripheral arteriesM Erren, H Reinecke, R Junker, et al.
Journal of Neurology|October 17, 1998
Prevalence of factor V Leiden mutation in young adults with cerebral ischaemia: a case-control study on 225 patientsD G Nabavi, R Junker, E Wolff, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 11, 2001
Atherosclerosis in apolipoprotein E-deficient mice is decreased by the suppression of endogenous sex hormonesG von Dehn, O von Dehn, W Völker, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|July 17, 2012
Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrationsSa Muntoni, H Wiebusch, M Jansen-Rust, et al.
Pacing and Clinical Electrophysiology : PACE|May 9, 2001
Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndromeG Moennig, E Schulze-Bahr, H Wedekind, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 28, 2001
ATP binding cassette transporter ABCA1 modulates the secretion of apolipoprotein E from human monocyte-derived macrophagesA Von Eckardstein, C Langer, T Engel, et al.
Gene|June 14, 1995
Prognostic relevance of aberrations in the erbB oncogenes from breast, ovarian, oral and lung cancers: double-differential polymerase chain reaction (ddPCR) for clinical diagnosisB Brandt, U Vogt, C M Schlotter, et al.
Neuroscience Letters|March 6, 1998
Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndromeF Stögbauer, P Young, H Wiebusch, et al.
The Journal of Clinical Investigation|December 1, 1995
A unique genetic and biochemical presentation of fish-eye diseaseJ A Kuivenhoven, E J van Voorst tot Voorst, H Wiebusch, et al.
Atherosclerosis|August 12, 1998
Modulated serum activities and concentrations of paraoxonase in high density lipoprotein deficiency statesR W James, M C Blatter Garin, L Calabresi, et al.
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