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Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|June 5, 1999
Characterization of subtypes of hypertension in CAPD patients by cyclic guanosine monophosphateS M Lang, G Wolfram, R Gerzer, et al.
European Journal of Clinical Investigation|June 1, 1983
Hormonal regulation of lipogenesis in human diploid fibroblasts from normal subjects and from patients with familial hypertriglyceridaemiaC Lemmen, G Wolfram, C A Barth, et al.
The Clinical Investigator|January 1, 1992
Familial defective apolipoprotein B-100: a common cause of primary hypercholesterolemiaG Rauh, C Keller, H Schuster, et al.
Bildgebung = Imaging|January 1, 1991
Echocardiographic changes in patients with heterozygous and homozygous familial hypercholesterolemia: correlation with clinical findingsF Tatò, C Keller, S Schewe, et al.
The Clinical Investigator|February 1, 1993
Identification of the serine-156 to leucine mutation in the low-density lipoprotein receptor in a German family with familial hypercholesterolemiaH Schuster, P Ostwald, P Keller, et al.
Das Offentliche Gesundheitswesen|February 1, 1989
[Nutrition survey of adults using a 7-day protocol--a pilot study in the Augsburg MONICA project]M Colling, S Weggemann, A Döring, et al.
Atherosclerosis|February 1, 1983
Xeroradiographic determination of Achilles tendon thickness in familial hypercholesterolemia confirmed by tissue culturesO Seidl, C Keller, H Berger, et al.
Clinical Nutrition (Edinburgh, Scotland)|July 15, 2000
Antioxidant status of surgical patients receiving TPN with an omega-3-fatty acid-containing lipid emulsion supplemented with alpha-tocopherolJ Linseisen, J Hoffmann, S Lienhard, et al.
Klinische Wochenschrift|November 15, 1991
Identification of a 76-year-old patient with compound heterozygous familial hypercholesterolemia by haplotype analysis of the LDL receptor geneH J Fischer, H Schuster, C Keller, et al.
Human Genetics|April 1, 1993
Identification of the 408 valine to methionine mutation in the low density lipoprotein receptor in a German family with familial hypercholesterolemiaH Schuster, H J Fischer, C Keller, et al.
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