Hach-Wunderle V - Search Results

1

Combined occurrence of a heterozygous missense mutation in the protein C gene and allelic exclusion of one protein S allele leading to severe venous thrombosis.

Knoll B, Hach-Wunderle V, Rieger S, Häring D, Mannhalter C. Knoll B, et al. Thromb Res. 2001 Jul 1;103(1):3-8. doi: 10.1016/s0049-3848(01)00232-8. Thromb Res. 2001. PMID: 11434940

2

Congenital deficiency of plasminogen and its relationship to venous thrombosis.

Hach-Wunderle V, Scharrer I, Lottenberg R. Hach-Wunderle V, et al. Thromb Haemost. 1988 Apr 8;59(2):277-80. Thromb Haemost. 1988. PMID: 3388298

3

[Venous thrombosis in pregnancy].

Hach-Wunderle V. Hach-Wunderle V. Vasa. 2003 May;32(2):61-8. doi: 10.1024/0301-1526.32.2.61. Vasa. 2003. PMID: 12945097 Review. German.

4

Impact of gender on the clinical presentation and diagnosis of deep-vein thrombosis.

Bauersachs RM, Riess H, Hach-Wunderle V, Gerlach H, Carnarius H, Eberle S, Rabe E, Schellong SM. Bauersachs RM, et al. Among authors: hach wunderle v. Thromb Haemost. 2010 Apr;103(4):710-7. doi: 10.1160/TH09-10-0705. Epub 2010 Feb 19. Thromb Haemost. 2010. PMID: 20174769

5

Congenital abnormal plasminogen, Frankfurt I, a cause for recurrent venous thrombosis.

Scharrer I, Hach-Wunderle V, Wohl RC, Sinio L, Boreisha I, Robbins KC. Scharrer I, et al. Haemostasis. 1988;18 Suppl 1:77-86. doi: 10.1159/000215841. Haemostasis. 1988. PMID: 2965086

6

[Disorders of the liberation of tissue-type plasminogen activator (t-PA) from the venous wall as a cause for recurrent thromboses].

Hach-Wunderle V, Scharrer I. Hach-Wunderle V, et al. Vasa Suppl. 1993;39:5-10. Vasa Suppl. 1993. PMID: 8322122 German.

7

[Prevalence of hereditary deficiency of antithrombin III, Protein C en Protein S].

Hach-Wunderle V, Scharrer I. Hach-Wunderle V, et al. Dtsch Med Wochenschr. 1993 Feb 12;118(6):187-90. doi: 10.1055/s-2008-1059317. Dtsch Med Wochenschr. 1993. PMID: 8436068 German. No abstract available.

8

[Prevention of venous thromboses with oral anticoagulants].

Hach-Wunderle V, Scharrer I. Hach-Wunderle V, et al. Wien Med Wochenschr. 1989 Dec 15;139(23):559-62. Wien Med Wochenschr. 1989. PMID: 2696215 Review. German.

9

Prevalence of elevated histidine-rich glycoprotein in patients with thrombophilia--a study of 695 patients.

Ehrenforth S, Aygören-Pürsün E, Hach-Wunderle V, Scharrer I. Ehrenforth S, et al. Thromb Haemost. 1994 Jan;71(1):160-1. Thromb Haemost. 1994. PMID: 8165641 No abstract available.

10

[Phenotypic healing of hemophilia A by liver transplantation].

Scharrer I, Encke A, Hottenrott C, Markus B, Klein G, Friedrich K, Ernst W, Hauser I, Kachel G, Hach-Wunderle V, et al. Scharrer I, et al. Med Klin (Munich). 1990 Mar;85 Suppl 1:116-8. Med Klin (Munich). 1990. PMID: 2160576 German. No abstract available.

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