Koch HG - Search Results

1

The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis.

Koch HG, Nabel P, Junker R, Auberger K, Schobess R, Homberger A, Linnebank M, Nowak-Göttl U. Koch HG, et al. Eur J Pediatr. 1999 Dec;158 Suppl 3:S113-6. doi: 10.1007/pl00014332. Eur J Pediatr. 1999. PMID: 10650848

2

Prospective evaluation of the thrombotic risk in children with acute lymphoblastic leukemia carrying the MTHFR TT 677 genotype, the prothrombin G20210A variant, and further prothrombotic risk factors.

Nowak-Göttl U, Wermes C, Junker R, Koch HG, Schobess R, Fleischhack G, Schwabe D, Ehrenforth S. Nowak-Göttl U, et al. Among authors: koch hg. Blood. 1999 Mar 1;93(5):1595-9. Blood. 1999. PMID: 10029588 Free article.

3

Prothrombin G20210A gene mutation and further prothrombotic risk factors in childhood thrombophilia.

Junker R, Koch HG, Auberger K, Münchow N, Ehrenforth S, Nowak-Göttl U. Junker R, et al. Among authors: koch hg. Arterioscler Thromb Vasc Biol. 1999 Oct;19(10):2568-72. doi: 10.1161/01.atv.19.10.2568. Arterioscler Thromb Vasc Biol. 1999. PMID: 10521389

4

Lipoprotein (a) and genetic polymorphisms of clotting factor V, prothrombin, and methylenetetrahydrofolate reductase are risk factors of spontaneous ischemic stroke in childhood.

Nowak-Göttl U, Sträter R, Heinecke A, Junker R, Koch HG, Schuierer G, von Eckardstein A. Nowak-Göttl U, et al. Among authors: koch hg. Blood. 1999 Dec 1;94(11):3678-82. Blood. 1999. PMID: 10572079 Free article.

5

Multicentre evaluation of combined prothrombotic defects associated with thrombophilia in childhood. Childhood Thrombophilia Study Group.

Ehrenforth S, Junker R, Koch HG, Kreuz W, Münchow N, Scharrer I, Nowak-Göttl U. Ehrenforth S, et al. Among authors: koch hg. Eur J Pediatr. 1999 Dec;158 Suppl 3:S97-104. doi: 10.1007/pl00014359. Eur J Pediatr. 1999. PMID: 10650845

6

A common haplotype for the 677T thermolabile variant of the 5,10-methylenetetrahydrofolate reductase gene in thrombophilic patients and controls.

Linnebank M, Homberger A, Nowak-Göttl U, Koch HG. Linnebank M, et al. Among authors: koch hg. Hum Mutat. 2002 Dec;20(6):478. doi: 10.1002/humu.9089. Hum Mutat. 2002. PMID: 12442281

7

Cerebral venous sinus thrombosis in infancy and childhood: role of genetic and acquired risk factors of thrombophilia.

Vielhaber H, Ehrenforth S, Koch HG, Scharrer I, van der Werf N, Nowak-Göttl U. Vielhaber H, et al. Among authors: koch hg. Eur J Pediatr. 1998 Jul;157(7):555-60. doi: 10.1007/s004310050877. Eur J Pediatr. 1998. PMID: 9686815

8

Increased lipoprotein(a) is an important risk factor for venous thromboembolism in childhood.

Nowak-Göttl U, Junker R, Hartmeier M, Koch HG, Münchow N, Assmann G, von Eckardstein A. Nowak-Göttl U, et al. Among authors: koch hg. Circulation. 1999 Aug 17;100(7):743-8. doi: 10.1161/01.cir.100.7.743. Circulation. 1999. PMID: 10449697

9

Anticoagulant response to Agkistrodon Contortrix venom (ACV) in infants and children with genetic defects in the protein C anticoagulant pathway.

Kirschbaum A, Junker R, Koch HG, Vielhaber H, Nowak-Göttl U. Kirschbaum A, et al. Among authors: koch hg. Eur J Pediatr. 1999 Dec;158 Suppl 3:S203-4. doi: 10.1007/pl00014356. Eur J Pediatr. 1999. PMID: 10650870 Clinical Trial. No abstract available.

10

Linkage disequilibrium of the common mutations 677C > T and 1298A > C of the human methylenetetrahydrofolate reductase gene as proven by the novel polymorphisms 129C > T, 1068C > T.

Linnebank M, Homberger A, Nowak-Göttl U, Marquardt T, Harms E, Koch HG. Linnebank M, et al. Among authors: koch hg. Eur J Pediatr. 2000 Jun;159(6):472-3. doi: 10.1007/s004310051311. Eur J Pediatr. 2000. PMID: 10867857 No abstract available.

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