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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.
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.
Science (New York, N.Y.)|May 30, 2009
A role for the CHC22 clathrin heavy-chain isoform in human glucose metabolismStéphane Vassilopoulos, Christopher Esk, Sachiko Hoshino, et al.
Clinical Genetics|September 17, 2013
A systematic approach to assessing the clinical significance of genetic variantsH Duzkale, J Shen, H McLaughlin, et al.
Cardiogenetics|September 25, 2013
Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variantQuinn S Wells, Natalie L Ausborn, Birgit H Funke, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Evaluation of single nucleotide polymorphisms in the phosphodiesterase 4D gene (PDE4D) and their association with ischaemic stroke in a large German cohortG Kuhlenbäumer, K Berger, A Huge, et al.
The Journal of Clinical Investigation|February 1, 1993
Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this diseaseH Funke, A von Eckardstein, P H Pritchard, 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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