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Influence of Dietary Linoleic Acid Intake with Different Fat Intakes on Arachidonic Acid Concentrations in Plasma and Platelet Lipids and Eicosanoid Biosynthesis in Female Volunteers

Annals of nutrition and metabolism, 2003-01, Vol.47 (1), p.31-36

2003

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Effect of alpha-linolenic acid in the human diet on linoleic acid metabolism and prostaglandin biosynthesis

Journal of lipid research, 1986-04, Vol.27 (4), p.421-426

1986

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Molecular Basis of AMP Deaminase Deficiency in Skeletal Muscle

Proceedings of the National Academy of Sciences - PNAS, 1992-07, Vol.89 (14), p.6457-6461

1992

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Independent mutation of arginine(3500)→glutamine associated with familial defective apolipoprotein B-100

Journal of lipid research, 1993-05, Vol.34 (5), p.799-805

1993

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Use of DNA haplotype analysis in diagnosis of familial hypercholesterolaemia in 31 German families

Journal of medical genetics, 1991-12, Vol.28 (12), p.865-870

1991

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Hyperuricemia

Der Internist (Berlin), 1995-12, Vol.36 (12), p.1207

1995

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Hyperuricemia

Urologe. Ausgabe A, 1996-05, Vol.35 (3), p.263

1996

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Influence of selective management on the prognosis and the risk of rupture of abdominal aortic aneurysms

The Clinical Investigator, 1994-08, Vol.72 (8), p.585-591

1994

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Diagnosis of familial hypercholesterolemia using DNA haplotype analysis in three large families with two hyperlipidemic parents

Annals of nutrition and metabolism, 1992, Vol.36 (2), p.79-86

1992

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Uricosuric effect of irtemazole in hyperuricemic patients without and with renal insufficiency

Zeitschrift für Rheumatologie, 1989-11, Vol.48 (6), p.307-312

1989

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Familial defective apolipoprotein B-100: Haplotype analysis of the arginine (3500) → glutamine mutation

Atherosclerosis, 1991-06, Vol.88 (2), p.219-226

1991

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Two forms of familial hypercholesterolemia: differences in cardiovascular risk factors, cardiac and extracardiac atherosclerosis

Deutsche medizinische Wochenschrift (1946), 2014-12, Vol.139 (50), p.2573

2014

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Prostaglandin formation in man during intake of different amounts of linoleic acid in formula diets

Annals of nutrition and metabolism, 1982-01, Vol.26 (5), p.315-323

1982

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Purine and pyrimidine metabolism

Proceedings of the Nutrition Society, 1982-09, Vol.41 (3), p.329-342

Zöllner, N

1982

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Familial defective apolipoprotein B100 : clinical characteristics of 54 cases

Atherosclerosis, 1992-02, Vol.92 (2-3), p.233-241

1992

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Serum cholesterol levels in patients with familial hypercholesterolemia confirmed by tissue culture

Atherosclerosis, 1981-04, Vol.39 (1), p.51-59

1981

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Fatty acid composition of the diet: impact on serum lipids and atherosclerosis

The Clinical Investigator, 1992-11, Vol.70 (11), p.968-1009

1992

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Serum levels of glucose, insulin, and C-peptide during long-term D-ribose administration in man

Klinische Wochenschrift, 1991-01, Vol.69 (1), p.31-36

1991

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Identification of the 408 valine to methionine mutation in the low density lipoprotein receptor in a German family with familial hypercholesterolemia

Human genetics, 1993-04, Vol.91 (3), p.287-289

1993

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Genetic evidence from 7 families that the apolipoprotein B gene is not involved in familial combined hyperlipidemia

Atherosclerosis, 1990-07, Vol.83 (1), p.81-87

1990

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Association of DNA-haplotypes in the human LDL-receptor gene with normal serum cholesterol levels

Clinical genetics, 1990-12, Vol.38 (6), p.401-409

1990

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Identification of defective binding of low density lipoprotein by the U937 proliferation assay in German patients with familial defective apolipoprotein B-100

European journal of clinical investigation, 1994-01, Vol.24 (1), p.36-41

1994

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Familial hypercholesterolemia and familial defective apolipoprotein B-100: comparison of the phenotypic expression In 116 cases

European journal of medical research, 1996-05, Vol.1 (8), p.383-386

1996

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Metabolism of D-ribose administered continuously to healthy persons and to patients with myoadenylate deaminase deficiency

Klinische Wochenschrift, 1989-12, Vol.67 (23), p.1205-1213

1989

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Use of fibroblast culture to diagnose and genotype familial hypercholesterolaemia

Annals of nutrition and metabolism, 1982, Vol.26 (4), p.240-247

1982

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Influence of Dietary Linoleic Acid Intake with Different Fat Intakes on Arachidonic Acid Concentrations in Plasma and Platelet Lipids and Eicosanoid Biosynthesis in Female Volunteers

Effect of alpha-linolenic acid in the human diet on linoleic acid metabolism and prostaglandin biosynthesis

Molecular Basis of AMP Deaminase Deficiency in Skeletal Muscle

Independent mutation of arginine(3500)→glutamine associated with familial defective apolipoprotein B-100

Use of DNA haplotype analysis in diagnosis of familial hypercholesterolaemia in 31 German families

Hyperuricemia

Hyperuricemia

Influence of selective management on the prognosis and the risk of rupture of abdominal aortic aneurysms

Diagnosis of familial hypercholesterolemia using DNA haplotype analysis in three large families with two hyperlipidemic parents

Uricosuric effect of irtemazole in hyperuricemic patients without and with renal insufficiency

Familial defective apolipoprotein B-100: Haplotype analysis of the arginine (3500) → glutamine mutation

Two forms of familial hypercholesterolemia: differences in cardiovascular risk factors, cardiac and extracardiac atherosclerosis

Prostaglandin formation in man during intake of different amounts of linoleic acid in formula diets

Purine and pyrimidine metabolism

Familial defective apolipoprotein B100 : clinical characteristics of 54 cases

Serum cholesterol levels in patients with familial hypercholesterolemia confirmed by tissue culture

Fatty acid composition of the diet: impact on serum lipids and atherosclerosis

Serum levels of glucose, insulin, and C-peptide during long-term D-ribose administration in man

Identification of the 408 valine to methionine mutation in the low density lipoprotein receptor in a German family with familial hypercholesterolemia

Genetic evidence from 7 families that the apolipoprotein B gene is not involved in familial combined hyperlipidemia

Association of DNA-haplotypes in the human LDL-receptor gene with normal serum cholesterol levels

Identification of defective binding of low density lipoprotein by the U937 proliferation assay in German patients with familial defective apolipoprotein B-100

Familial hypercholesterolemia and familial defective apolipoprotein B-100: comparison of the phenotypic expression In 116 cases

Metabolism of D-ribose administered continuously to healthy persons and to patients with myoadenylate deaminase deficiency

Use of fibroblast culture to diagnose and genotype familial hypercholesterolaemia

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