Mannhalter C - Search Results

1

Determinants of factor VIII plasma levels in carriers of haemophilia A and in control women.

Ay C, Thom K, Abu-Hamdeh F, Horvath B, Quehenberger P, Male C, Mannhalter C, Pabinger I. Ay C, et al. Among authors: mannhalter c. Haemophilia. 2010 Jan;16(1):111-7. doi: 10.1111/j.1365-2516.2009.02108.x. Epub 2009 Sep 16. Haemophilia. 2010. PMID: 19758307

2

Spectrum of causative mutations in patients with haemophilia A in Austria.

Reitter S, Sturn R, Horvath B, Freitag R, Male C, Muntean W, Streif W, Pabinger I, Mannhalter C; Austrian Molecular Haemophilia Study Group. Reitter S, et al. Among authors: mannhalter c. Thromb Haemost. 2010 Jul;104(1):78-85. doi: 10.1160/TH09-11-0795. Epub 2010 Apr 29. Thromb Haemost. 2010. PMID: 20431853

3

Parameters influencing FVIII pharmacokinetics in patients with severe and moderate haemophilia A.

Kepa S, Horvath B, Reitter-Pfoertner S, Schemper M, Quehenberger P, Grundbichler M, Heistinger M, Neumeister P, Mannhalter C, Pabinger I. Kepa S, et al. Among authors: mannhalter c. Haemophilia. 2015 May;21(3):343-350. doi: 10.1111/hae.12592. Epub 2015 Jan 13. Haemophilia. 2015. PMID: 25582282

4

High proportion of patients with bleeding of unknown cause in persons with a mild-to-moderate bleeding tendency: Results from the Vienna Bleeding Biobank (VIBB).

Gebhart J, Hofer S, Panzer S, Quehenberger P, Sunder-Plassmann R, Hoermann G, Eigenbauer E, Haslacher H, Kepa S, Kyrle PA, Eichinger S, Knöbl P, Eischer L, Mannhalter C, Ay C, Pabinger I. Gebhart J, et al. Among authors: mannhalter c. Haemophilia. 2018 May;24(3):405-413. doi: 10.1111/hae.13422. Epub 2018 Feb 1. Haemophilia. 2018. PMID: 29388750

5

The angiotensin-converting enzyme insertion/deletion polymorphism and serum levels of angiotensin-converting enzyme in venous thromboembolism. Data from a case control study.

Ay C, Bencur P, Vormittag R, Sailer T, Jungbauer C, Vukovich T, Mannhalter C, Pabinger I. Ay C, et al. Among authors: mannhalter c. Thromb Haemost. 2007 Oct;98(4):777-82. Thromb Haemost. 2007. PMID: 17938801

6

Inhibitor development in two patients with mild haemophilia A - spontaneous disappearance and no recurrence of the inhibitor after re-challenge.

Reitter-Pfoertner S, Horvath B, Lechner K, Sunder-Plassmann R, Mannhalter C, Pabinger I. Reitter-Pfoertner S, et al. Among authors: mannhalter c. Wien Klin Wochenschr. 2012 Mar;124(5-6):198-201. doi: 10.1007/s00508-011-0116-7. Epub 2012 Jan 18. Wien Klin Wochenschr. 2012. PMID: 22249861

7

Identification of an ancient haemophilia A splice site mutation.

Reitter-Pfoertner S, von Haeseler A, Horvath B, Sunder-Plassmann R, Tiedje V, Pabinger I, Mannhalter C. Reitter-Pfoertner S, et al. Among authors: mannhalter c. Thromb Res. 2012 Sep;130(3):445-50. doi: 10.1016/j.thromres.2012.02.008. Epub 2012 Mar 6. Thromb Res. 2012. PMID: 22401796

8

FVIII-binding IgG modulates FVIII half-life in patients with severe and moderate hemophilia A without inhibitors.

Hofbauer CJ, Kepa S, Schemper M, Quehenberger P, Reitter-Pfoertner S, Mannhalter C, Reipert BM, Pabinger I. Hofbauer CJ, et al. Among authors: mannhalter c. Blood. 2016 Jul 14;128(2):293-6. doi: 10.1182/blood-2015-10-675512. Epub 2016 May 23. Blood. 2016. PMID: 27216215 Free article.

9

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.

10

Low-density lipoprotein receptor-related protein 1 polymorphism 663 C > T affects clotting factor VIII activity and increases the risk of venous thromboembolism.

Vormittag R, Bencur P, Ay C, Tengler T, Vukovich T, Quehenberger P, Mannhalter C, Pabinger I. Vormittag R, et al. Among authors: mannhalter c. J Thromb Haemost. 2007 Mar;5(3):497-502. doi: 10.1111/j.1538-7836.2007.02337.x. Epub 2006 Nov 28. J Thromb Haemost. 2007. PMID: 17155964 Free article.

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