Koch M - Search Results

1

Association between angiotensin I-converting enzyme genotypes, extracranial artery stenosis, and stroke.

Pfohl M, Fetter M, Koch M, Barth CM, Rüdiger W, Häring HU. Pfohl M, et al. Among authors: koch m. Atherosclerosis. 1998 Sep;140(1):161-6. doi: 10.1016/s0021-9150(98)00100-2. Atherosclerosis. 1998. PMID: 9733227

2

Insertion/deletion polymorphism of the angiotensin I-converting enzyme gene is associated with coronary artery plaque calcification as assessed by intravascular ultrasound.

Pfohl M, Athanasiadis A, Koch M, Clemens P, Benda N, Häring HU, Karsch KR. Pfohl M, et al. Among authors: koch m. J Am Coll Cardiol. 1998 Apr;31(5):987-91. doi: 10.1016/s0735-1097(98)00044-8. J Am Coll Cardiol. 1998. PMID: 9561998 Free article.

3

Lack of association between the insertion/deletion polymorphism of the angiotensin-converting-enzyme gene and diabetic nephropathy in IDDM patients.

Pfohl M, Frost D, Koch M, Clemens P, Patzies A, Schmülling RM, Beischer W, Häring HU. Pfohl M, et al. Among authors: koch m. Horm Metab Res. 1998 May;30(5):276-80. doi: 10.1055/s-2007-978883. Horm Metab Res. 1998. PMID: 9660089

4

Angiotensin I-converting enzyme gene polymorphism, coronary artery disease and myocardial infarction. An angiographically controlled study.

Pfohl M, Koch M, Prescod S, Haase KK, Häring HU, Karsch KR. Pfohl M, et al. Among authors: koch m. Eur Heart J. 1999 Sep;20(18):1318-25. doi: 10.1053/euhj.1999.1543. Eur Heart J. 1999. PMID: 10462466

5

Paraoxonase 192 Gln/Arg gene polymorphism, coronary artery disease, and myocardial infarction in type 2 diabetes.

Pfohl M, Koch M, Enderle MD, Kühn R, Füllhase J, Karsch KR, Häring HU. Pfohl M, et al. Among authors: koch m. Diabetes. 1999 Mar;48(3):623-7. doi: 10.2337/diabetes.48.3.623. Diabetes. 1999. PMID: 10078566

6

Paraoxonase 1 192 Gln/Arg gene polymorphism and cerebrovascular disease: interaction with type 2 diabetes.

Koch M, Hering S, Barth C, Ehren M, Enderle MD, Pfohl M. Koch M, et al. Exp Clin Endocrinol Diabetes. 2001;109(3):141-5. doi: 10.1055/s-2001-14836. Exp Clin Endocrinol Diabetes. 2001. PMID: 11409295

7

Analysis of the deletion/insertion polymorphism of the angiotensin I-converting enzyme gene by capillary electrophoresis.

Koch M, Lehmann R, Pfohl M, Voelter W, Liebich H. Koch M, et al. Clin Chim Acta. 1996 Apr 30;248(2):197-203. doi: 10.1016/0009-8981(95)06255-6. Clin Chim Acta. 1996. PMID: 8740583 No abstract available.

8

Screening and identification of familial defective apolipoprotein B-100 in clinical samples by capillary gel electrophoresis.

Lehmann R, Koch M, Pfohl M, Voelter W, Häring HU, Liebich HM. Lehmann R, et al. Among authors: koch m. J Chromatogr A. 1996 Sep 13;744(1-2):187-94. doi: 10.1016/0021-9673(96)00244-0. J Chromatogr A. 1996. PMID: 8843667

9

The tumour necrosis factor alpha -238 G --> A and -308 G --> A promoter polymorphisms are not associated with insulin sensitivity and insulin secretion in young healthy relatives of Type II diabetic patients.

Koch M, Rett K, Volk A, Maerker E, Haist K, Weisser M, Rettig A, Renn W, Häring HU. Koch M, et al. Diabetologia. 2000 Feb;43(2):181-4. doi: 10.1007/s001250050027. Diabetologia. 2000. PMID: 10753039

10

The PPARgamma2 amino acid polymorphism Pro 12 Ala is prevalent in offspring of Type II diabetic patients and is associated to increased insulin sensitivity in a subgroup of obese subjects.

Koch M, Rett K, Maerker E, Volk A, Haist K, Deninger M, Renn W, Häring HU. Koch M, et al. Diabetologia. 1999 Jun;42(6):758-62. doi: 10.1007/s001250051225. Diabetologia. 1999. PMID: 10382597

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