Vielhaber H - Search Results

1

The plasminogen activator inhibitor (PAI)-1 promoter 4G/4G genotype is not associated with ischemic stroke in a population of German children. Childhood Stroke Study Group.

Nowak-Göttl U, Sträter R, Kosch A, von Eckardstein A, Schobess R, Luigs P, Nabel P, Vielhaber H, Kurnik K, Junker R. Nowak-Göttl U, et al. Among authors: vielhaber h. Eur J Haematol. 2001 Jan;66(1):57-62. doi: 10.1034/j.1600-0609.2001.00338.x. Eur J Haematol. 2001. PMID: 11168509

2

Elevated levels of soluble thrombomodulin in plasma from children with Arg 506 to Gln mutation in the factor V gene.

Nowak-Göttl U, Vielhaber H. Nowak-Göttl U, et al. Among authors: vielhaber h. Eur J Haematol. 1997 Jan;58(1):51-5. doi: 10.1111/j.1600-0609.1997.tb01410.x. Eur J Haematol. 1997. PMID: 9020374

3

Genetic risk factors of thrombophilia in ischaemic childhood stroke of cardiac origin. A prospective ESPED survey.

Sträter R, Vielhaber H, Kassenböhmer R, von Kries R, Göbel U, Nowak-Göttl U. Sträter R, et al. Among authors: vielhaber h. Eur J Pediatr. 1999 Dec;158 Suppl 3:S122-5. doi: 10.1007/pl00014336. Eur J Pediatr. 1999. PMID: 10650850

4

Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease.

Junker R, Kotthoff S, Vielhaber H, Halimeh S, Kosch A, Koch HG, Kassenböhmer R, Heineking B, Nowak-Göttl U. Junker R, et al. Among authors: vielhaber h. Cardiovasc Res. 2001 Aug 1;51(2):251-4. doi: 10.1016/s0008-6363(01)00286-3. Cardiovasc Res. 2001. PMID: 11470464

5

Ischaemic stroke in infancy and childhood: role of the Arg506 to Gln mutation in the factor V gene.

Nowak-Göttl U, Sträter R, Dübbers A, Oleszuk-Raschke K, Vielhaber H. Nowak-Göttl U, et al. Among authors: vielhaber h. Blood Coagul Fibrinolysis. 1996 Oct;7(7):684-8. Blood Coagul Fibrinolysis. 1996. PMID: 8958390

6

Arginine506 to glutamin mutation in the factor V gene in infancy and childhood: evidence of fibrinolytic impairment.

Nowak-Göttl U, Vielhaber H, Grohmann J, Schneppenheim R, Koch HG. Nowak-Göttl U, et al. Among authors: vielhaber h. Eur J Pediatr. 1997 Mar;156(3):195-8. doi: 10.1007/s004310050581. Eur J Pediatr. 1997. PMID: 9083758

7

APC resistance in childhood thromboembolism: diagnosis and clinical aspects.

Nowak-Göttl U, Schneppenheim R, Vielhaber H. Nowak-Göttl U, et al. Among authors: vielhaber h. Semin Thromb Hemost. 1997;23(3):253-8. doi: 10.1055/s-2007-996098. Semin Thromb Hemost. 1997. PMID: 9255906 Review.

8

Factor V Leiden and genetic defects of thrombophilia in childhood porencephaly.

Debus O, Koch HG, Kurlemann G, Sträter R, Vielhaber H, Weber P, Nowak-Göttl U. Debus O, et al. Among authors: vielhaber h. Arch Dis Child Fetal Neonatal Ed. 1998 Mar;78(2):F121-4. doi: 10.1136/fn.78.2.f121. Arch Dis Child Fetal Neonatal Ed. 1998. PMID: 9577282 Free PMC article.

9

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

10

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: vielhaber h. 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.

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