Schuster H - Search Results

1

Phenotypic variation in patients heterozygous for familial defective apolipoprotein B (FDB) in three European countries.

Hansen PS, Defesche JC, Kastelein JJ, Gerdes LU, Fraza L, Gerdes C, Tato F, Jensen HK, Jensen LG, Klausen IC, Faergeman O, Schuster H. Hansen PS, et al. Among authors: schuster h. Arterioscler Thromb Vasc Biol. 1997 Apr;17(4):741-7. doi: 10.1161/01.atv.17.4.741. Arterioscler Thromb Vasc Biol. 1997. PMID: 9108789

2

Screening for familial defective apolipoprotein B-100 with improved U937 monocyte proliferation assay.

Van den Broek AJ, Hollaar L, Schaefer HI, Van der Laarse A, Schuster H, Defesche JC, Kastelein JJ, Van 't Hooft FM. Van den Broek AJ, et al. Among authors: schuster h. Clin Chem. 1994 Mar;40(3):395-9. Clin Chem. 1994. PMID: 8131274

3

Relation of lipoprotein(a) to coronary heart disease and duplexsonographic findings of the carotid arteries in heterozygous familial hypercholesterolemia.

Tatò F, Keller C, Schuster H, Spengel F, Wolfram G, Zöllner N. Tatò F, et al. Among authors: schuster h. Atherosclerosis. 1993 Jun;101(1):69-77. doi: 10.1016/0021-9150(93)90103-2. Atherosclerosis. 1993. PMID: 8216504

4

Screening for the apolipoprotein B-100 arginine3500-->glutamine mutation in patients with type III hyperlipoproteinemia.

Feussner G, Schuster H. Feussner G, et al. Among authors: schuster h. Clin Genet. 1992 Dec;42(6):302-5. doi: 10.1111/j.1399-0004.1992.tb03260.x. Clin Genet. 1992. PMID: 1493642

5

Familial defective apolipoprotein B-100. Comparison with familial hypercholesterolemia in 18 cases detected in Munich.

Schuster H, Rauh G, Kormann B, Hepp T, Humphries S, Keller C, Wolfram G, Zöllner N. Schuster H, et al. Arteriosclerosis. 1990 Jul-Aug;10(4):577-81. doi: 10.1161/01.atv.10.4.577. Arteriosclerosis. 1990. PMID: 2164382

6

Ten LDL receptor mutants explain one third of familial hypercholesterolemia in a German sample.

Schuster H, Keller C, Wolfram G, Zöllner N. Schuster H, et al. Arterioscler Thromb Vasc Biol. 1995 Dec;15(12):2176-80. doi: 10.1161/01.atv.15.12.2176. Arterioscler Thromb Vasc Biol. 1995. PMID: 7489239

7

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

Brugger D, Schuster H, Zöllner N. Brugger D, et al. Among authors: schuster h. Eur J Med Res. 1996 May 24;1(8):383-6. Eur J Med Res. 1996. PMID: 9360938

8

Heritability analysis of lipids and three gene loci in twins link the macrophage scavenger receptor to HDL cholesterol concentrations.

Knoblauch H, Busjahn A, Münter S, Nagy Z, Faulhaber HD, Schuster H, Luft FC. Knoblauch H, et al. Among authors: schuster h. Arterioscler Thromb Vasc Biol. 1997 Oct;17(10):2054-60. doi: 10.1161/01.atv.17.10.2054. Arterioscler Thromb Vasc Biol. 1997. PMID: 9351371

9

Familial defective apolipoprotein B100: clinical characteristics of 54 cases.

Rauh G, Keller C, Kormann B, Spengel F, Schuster H, Wolfram G, Zöllner N. Rauh G, et al. Among authors: schuster h. Atherosclerosis. 1992 Feb;92(2-3):233-41. doi: 10.1016/0021-9150(92)90283-m. Atherosclerosis. 1992. PMID: 1632851

10

The effect of the apolipoprotein E polymorphism on lipid levels in patients with familial defective apolipoprotein B-100.

Manke C, Schuster H, Keller C, Wolfram G. Manke C, et al. Among authors: schuster h. Clin Investig. 1993 Apr;71(4):277-80. doi: 10.1007/BF00184726. Clin Investig. 1993. PMID: 8471813

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