Mannhalter C - Search Results

1

[Transgenic foods--advantages and risks].

Mannhalter C. Mannhalter C. Wien Klin Wochenschr. 1997 Jan 31;109(2):33-9. Wien Klin Wochenschr. 1997. PMID: 9123942 Review. German. No abstract available.

2

[Molecular genetic studies in the von Willebrand's syndrome].

Mannhalter C, Parzer S, Kyrle PA. Mannhalter C, et al. Wien Klin Wochenschr. 1990 Sep 14;102(17):491-6. Wien Klin Wochenschr. 1990. PMID: 1979896 German.

3

[Practice guidelines for formulation of patient or subject information and for the declaration of consent in genetic studies (inclusive of pharmaceutical genetics].

Mannhalter C, Druml C, Singer EA; Ethik-Kommission der Medizinischen Fakultät der Universität Wien und des Allgemeinen Krankenhauses der Stadt Wien-AKH. Mannhalter C, et al. Wien Klin Wochenschr. 2001 Nov 15;113(22):867-9. Wien Klin Wochenschr. 2001. PMID: 11762123 German. No abstract available.

4

[Molecular biology of tobacco smoke associated neoplasia].

Zojer N, Fritsche R, Fiegl M, Schulte-Hermann R, Mannhalter C, Huber H. Zojer N, et al. Among authors: mannhalter c. Wien Klin Wochenschr. 1996;108(18):574-81. Wien Klin Wochenschr. 1996. PMID: 9012141 Review. German.

5

Chronic myeloid leukemia: pathophysiology, diagnostic parameters, and current treatment concepts.

Sillaber C, Mayerhofer M, Agis H, Sagaster V, Mannhalter C, Sperr WR, Geissler K, Valent P. Sillaber C, et al. Among authors: mannhalter c. Wien Klin Wochenschr. 2003 Aug 14;115(13-14):485-504. doi: 10.1007/BF03041033. Wien Klin Wochenschr. 2003. PMID: 13677268 Review.

6

[Factor XII (Hageman factor) deficiency: a risk factor for development of thromboembolism. Incidence of factor XII deficiency in patients after recurrent venous or arterial thromboembolism and myocardial infarction].

Halbmayer WM, Mannhalter C, Feichtinger C, Rubi K, Fischer M. Halbmayer WM, et al. Among authors: mannhalter c. Wien Med Wochenschr. 1993;143(2):43-50. Wien Med Wochenschr. 1993. PMID: 8488686 German.

7

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

8

Rapid neonatal diagnosis of type IIB von Willebrand disease using the polymerase chain reaction.

Mannhalter C, Kyrle PA, Brenner B, Lechner K. Mannhalter C, et al. Blood. 1991 Jun 1;77(11):2539-40. Blood. 1991. PMID: 1674891 Free article. No abstract available.

9

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

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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