Mannhalter C - Search Results

1

Oral contraceptives enhance the risk of clinical manifestation of venous thrombosis at a young age in females homozygous for factor V Leiden.

Rintelen C, Mannhalter C, Ireland H, Lane DA, Knöbl P, Lechner K, Pabinger I. Rintelen C, et al. Among authors: mannhalter c. Br J Haematol. 1996 May;93(2):487-90. doi: 10.1046/j.1365-2141.1996.5712013.x. Br J Haematol. 1996. PMID: 8639453

2

Probability of recurrence of thrombosis in patients with and without factor V Leiden.

Rintelen C, Pabinger I, Knöbl P, Lechner K, Mannhalter C. Rintelen C, et al. Among authors: mannhalter c. Thromb Haemost. 1996 Feb;75(2):229-32. Thromb Haemost. 1996. PMID: 8815565

3

Thrombotic tendency in 75 symptomatic, unrelated patients with APC resistance.

Melichart M, Kyrle PA, Eichinger S, Rintelen C, Mannhalter C, Pabinger I. Melichart M, et al. Among authors: mannhalter c. Wien Klin Wochenschr. 1996;108(19):607-10. Wien Klin Wochenschr. 1996. PMID: 8921576

4

The risk of recurrent venous thromboembolism in patients with and without factor V Leiden.

Eichinger S, Pabinger I, Stümpflen A, Hirschl M, Bialonczyk C, Schneider B, Mannhalter C, Minar E, Lechner K, Kyrle PA. Eichinger S, et al. Among authors: mannhalter c. Thromb Haemost. 1997 Apr;77(4):624-8. Thromb Haemost. 1997. PMID: 9134632 Clinical Trial.

5

A frequent mutation in the protein S gene results in cryptic splicing.

Mustafa S, Pabinger I, Mannhalter C. Mustafa S, et al. Among authors: mannhalter c. Br J Haematol. 1997 Jun;97(3):555-7. doi: 10.1046/j.1365-2141.1997.962912.x. Br J Haematol. 1997. PMID: 9207399 Free article.

6

A hitherto unknown splice site defect in the protein S gene (PROS1): the mutation results in allelic exclusion and causes type I and type III protein S deficiency.

Mustafa S, Pabinger I, Vàradi K, Halbmayer WM, Lechner K, Schwarz HP, Fischer M, Mannhalter C. Mustafa S, et al. Among authors: mannhalter c. Br J Haematol. 1997 Nov;99(2):298-300. doi: 10.1046/j.1365-2141.1997.3883202.x. Br J Haematol. 1997. PMID: 9375743 Free article.

7

Clinical features of thrombophilia in families with gene defects in protein C or protein S combined with factor V Leiden.

Mustafa S, Mannhalter C, Rintelen C, Kyrle PA, Knöbl P, Lechner K, Pabinger I. Mustafa S, et al. Among authors: mannhalter c. Blood Coagul Fibrinolysis. 1998 Jan;9(1):85-9. doi: 10.1097/00001721-199801000-00011. Blood Coagul Fibrinolysis. 1998. PMID: 9607123

8

No evidence for an increased risk of venous thrombosis in patients with factor V Leiden by the homozygous 677 C to T mutation in the methylenetetrahydrofolate-reductase gene.

Rintelen C, Mannhalter C, Lechner K, Eichinger S, Kyrle PA, Papagiannopoulos M, Schneider B, Pabinger I. Rintelen C, et al. Among authors: mannhalter c. Blood Coagul Fibrinolysis. 1999 Mar;10(2):101-5. doi: 10.1097/00001721-199903000-00007. Blood Coagul Fibrinolysis. 1999. PMID: 10192659

9

Homocysteine levels in polycythaemia vera and essential thrombocythaemia.

Gisslinger H, Rodeghiero F, Ruggeri M, Heis-Vahidi Fard N, Mannhalter C, Papagiannopoulos M, Rintelen C, Lalouschek W, Knöbl P, Lechner K, Pabinger I. Gisslinger H, et al. Among authors: mannhalter c. Br J Haematol. 1999 May;105(2):551-5. Br J Haematol. 1999. PMID: 10233436 Free article.

10

Impact of the factor II: G20210A variant on the risk of venous thromboembolism in relatives from families with the factor V: R506Q mutation.

Rintelen C, Pabinger I, Bettelheim P, Lechner K, Kyrle PA, Knöbl P, Schneider B, Mannhalter C. Rintelen C, et al. Among authors: mannhalter c. Eur J Haematol. 2001 Sep;67(3):165-9. doi: 10.1034/j.1600-0609.2001.5790460.x. Eur J Haematol. 2001. PMID: 11737249

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