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Showing results (71-80 of 76) with videos related to

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The Journal of Pathology|June 13, 2006
Human endothelial cell septins: SEPT11 is an interaction partner of SEPT5S Bläser, S Röseler, H Rempp, et al.
Klinische Padiatrie|June 2, 2010
Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type IC Vannier, W Behnisch, I Bartsch, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 29, 2009
Novel findings in two patients with late-diagnosed afibrinogenaemia: intraosseous haemorrhage and fingertip necrosisM Erlacher, J Heiss, I Hainmann, et al.
Thrombosis and Haemostasis|February 11, 2000
Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 familiesR Schneppenheim, A B Federici, U Budde, et al.
Hamostaseologie|June 7, 2014
[Diagnosis of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)]R Knöfler, W Eberl, H Schulze, et al.
Hamostaseologie|November 6, 2014
[Therapy of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)]W Streif, R Knöfler, W Eberl, et al.
Pageof 8

Showing results (71-80 of 76) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 76 results.
The Journal of Pathology|June 13, 2006
Human endothelial cell septins: SEPT11 is an interaction partner of SEPT5S Bläser, S Röseler, H Rempp, et al.
Klinische Padiatrie|June 2, 2010
Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type IC Vannier, W Behnisch, I Bartsch, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 29, 2009
Novel findings in two patients with late-diagnosed afibrinogenaemia: intraosseous haemorrhage and fingertip necrosisM Erlacher, J Heiss, I Hainmann, et al.
Thrombosis and Haemostasis|February 11, 2000
Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 familiesR Schneppenheim, A B Federici, U Budde, et al.
Hamostaseologie|June 7, 2014
[Diagnosis of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)]R Knöfler, W Eberl, H Schulze, et al.
Hamostaseologie|November 6, 2014
[Therapy of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)]W Streif, R Knöfler, W Eberl, et al.
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