Ehrenforth S - Search Results

1

Study of the prothrombin gene 20201 GA variant in FV:Q506 carriers in relationship to the presence or absence of juvenile venous thromboembolism.

Ehrenforth S, von Depka Prondsinski M, Aygören-Pürsün E, Nowak-Göttl U, Scharrer I, Ganser A. Ehrenforth S, et al. Arterioscler Thromb Vasc Biol. 1999 Feb;19(2):276-80. doi: 10.1161/01.atv.19.2.276. Arterioscler Thromb Vasc Biol. 1999. PMID: 9974407

2

[Activated protein C resistance and venous thrombophilia: molecular genetic prevalence study in the German population].

Ehrenforth S, Klinke S, von Depka Prondzinski M, Kreuz W, Ganser A, Scharrer I. Ehrenforth S, et al. Dtsch Med Wochenschr. 1999 Jun 25;124(25-26):783-7. doi: 10.1055/s-2007-1024412. Dtsch Med Wochenschr. 1999. PMID: 10414227 German.

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: ehrenforth s. 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

The deletion polymorphism in the angiotensin-converting enzyme gene is a moderate risk factor for venous thromboembolism.

von Depka M, Czwalinna A, Wermes C, Eisert R, Scharrer I, Ganser A, Ehrenforth S. von Depka M, et al. Among authors: ehrenforth s. Thromb Haemost. 2003 May;89(5):847-52. Thromb Haemost. 2003. PMID: 12719783

5

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: ehrenforth s. Eur J Pediatr. 1998 Jul;157(7):555-60. doi: 10.1007/s004310050877. Eur J Pediatr. 1998. PMID: 9686815

6

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: ehrenforth s. Blood. 1999 Mar 1;93(5):1595-9. Blood. 1999. PMID: 10029588 Free article.

7

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. Eur J Pediatr. 1999 Dec;158 Suppl 3:S97-104. doi: 10.1007/pl00014359. Eur J Pediatr. 1999. PMID: 10650845

8

Increased lipoprotein (a) levels as an independent risk factor for venous thromboembolism.

von Depka M, Nowak-Göttl U, Eisert R, Dieterich C, Barthels M, Scharrer I, Ganser A, Ehrenforth S. von Depka M, et al. Among authors: ehrenforth s. Blood. 2000 Nov 15;96(10):3364-8. Blood. 2000. PMID: 11071628 Free article.

9

Prevalence of a 23bp insertion in exon 3 of the endothelial cell protein C receptor gene in venous thrombophilia.

von Depka M, Czwalinna A, Eisert R, Wermes C, Scharrer I, Ganser A, Ehrenforth S. von Depka M, et al. Among authors: ehrenforth s. Thromb Haemost. 2001 Dec;86(6):1360-2. Thromb Haemost. 2001. PMID: 11776299

10

Impact of environmental and hereditary risk factors on the clinical manifestation of thrombophilia in homozygous carriers of factor V:G1691A.

Ehrenforth S, Nemes L, Mannhalter C, Rosendaal FR, Koder S, Zoghlami-Rintelen C, Scharrer I, Pabinger I. Ehrenforth S, et al. J Thromb Haemost. 2004 Mar;2(3):430-6. doi: 10.1111/j.1538-7836.2004.00606.x. J Thromb Haemost. 2004. PMID: 15009459 Free article.

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