E. Pollak

发表

Endothelial cells in physiology and in the pathophysiology of vascular disorders.

J. Loscalzo, J. Pober, D. Cines, 1998, Blood.

Severe factor VII deficiency due to a mutation disrupting an Sp1 binding site in the factor VII promoter.

K. Bauer, K. High, E. Pollak, 1998, Blood.

Severe Factor VII Deficiency Due to a Mutation Disrupting an Sp1 Binding Site in the Factor VII Promoter

K. Bauer, K. High, E. Pollak, 1998 .

A new mutation in the HNF4 binding region of the factor VII promoter in a patient with severe factor VII deficiency.

K. Bauer, S. Lopaciuk, E. Pollak, 2000, Blood.

Severe factor VII deficiency due to a mutation disrupting a hepatocyte nuclear factor 4 binding site in the factor VII promoter.

J. Bayleran, A. Arbini, K. Bauer, 1997 .

Factor VII mutant V154G models a zymogen-like form of factor VIIa.

F. Bernardi, M. Pinotti, G. Marchetti, 2003, The Biochemical journal.

Increased ADAMTS‐13 proteolytic activity in rat hepatic stellate cells upon activation in vitro and in vivo

R. Wells, M. Uemura, E. Pollak, 2006, Journal of thrombosis and haemostasis : JTH.

Clinical presentation and laboratory diagnosis of heparin-induced thrombocytopenia.

C. Abrams, E. Pollak, 2005, Seminars in thoracic and cardiovascular surgery.

Serologic Results in >1000 Patients With Suspected Heparin-Induced Thrombocytopenia

E. Pollak, A. Tomaski, S. Shelat, 2008, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

A novel missense mutation responsible for factor VII deficiency in research Beagle colonies

U. Giger, P. Margaritis, K. High, 2006, Journal of thrombosis and haemostasis : JTH.

The G20210A mutation does not affect the stability of prothrombin mRNA in vivo.

E. Pollak, J. E. Russell, Ho-Sun Lam, 2002, Blood.

Interlaboratory agreement in the monitoring of unfractionated heparin using the anti‐factor Xa‐correlated activated partial thromboplastin time

D. Cines, B. Konkle, S. Pipe, 2009, Journal of thrombosis and haemostasis : JTH.

Multiple variables affecting blood usage in lung transplantation.

S. Sonnad, L. Kaiser, J. Christie, 2006, The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation.

and the Sp family of transcription factors Regulation of human coagulation factor X gene expression by GATA-4

V. Arruda, E. Pollak, K. Chu, 2013 .

Characterization of mild coagulation factor VII deficiency: activity and clearance of the Arg315Trp and Arg315Lys variants in the Cys310-Cys329 loop (c170s).

F. Bernardi, M. Pinotti, V. Arruda, 2004, Haematologica.

Rapid detection of the prothrombin C20209T variant by differential sensitivity to restriction endonuclease digestion

M. Ozelo, J. Annichino-Bizzacchi, E. Pollak, 2003, Journal of thrombosis and haemostasis : JTH.

Platelet glycoprotein Ibα polymorphisms modulate the risk for myocardial infarction

M. Ozelo, F. Costa, V. Arruda, 2004, Thrombosis and Haemostasis.

Utility of D‐dimer in the diagnosis of cerebral venous sinus thrombosis

B. Cucchiara, S. Messé, E. Pollak, 2005, Journal of thrombosis and haemostasis : JTH.

Mutation in the factor VII hepatocyte nuclear factor 4&agr;-binding site contributes to factor VII deficiency

P. Margaritis, E. Pollak, D. DiMichele, 2011, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.