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European Journal of Clinical Pharmacology|January 1, 1986
Effect of acarbose on carbohydrate tolerance during administration of a fibre-free formula diet on healthy subjectsI E Walter-Sack, A Ittner-Holland, G Wolfram, et al.
Hearing Research|August 1, 1997
Transcripts encoding three types of guanylyl-cyclase-coupled trans-membrane receptors in inner ear tissues of guinea pigsG Krause, A M Meyer zum Gottesberge, G Wolfram, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|June 1, 1988
Evidence for a nonspecific factor interfering in the radioimmunoassay of somatoliberin-like immunoreactivity in human seminal plasmaM Losa, G Wolfram, J Schopohl, et al.
Biological Psychiatry|May 1, 1990
Disturbances in the hypothalamo-pituitary-adrenal and other neuroendocrine axes in bulimiaM M Fichter, K M Pirke, J Pöllinger, et al.
Clinical Genetics|August 1, 1995
Identification of the valine 408 to methionine mutation in the LDL receptor in a Greek patient with homozygous familial hypercholesterolemiaH Schuster, C Manke, J Fischer, et al.
Journal of Medical Genetics|December 1, 1991
Use of DNA haplotype analysis in diagnosis of familial hypercholesterolaemia in 31 German familiesH Schuster, G Rauh, C Gerl, et al.
Atherosclerosis|June 1, 1991
Familial defective apolipoprotein B-100: haplotype analysis of the arginine(3500)----glutamine mutationG Rauh, H Schuster, J Fischer, et al.
Annals of Dyslexia|February 25, 2009
The role of gene DCDC2 in German dyslexicsA Wilcke, J Weissfuss, H Kirsten, et al.
Atherosclerosis|June 1, 1993
Relation of lipoprotein(a) to coronary heart disease and duplexsonographic findings of the carotid arteries in heterozygous familial hypercholesterolemiaF Tatò, C Keller, H Schuster, et al.
Klinische Wochenschrift|May 3, 1991
Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100G Rauh, H Schuster, J Fischer, et al.
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