M. Ledford

发表

Effects of severe, uncontrolled hypertension on endothelial activation: soluble vascular cell adhesion molecule-1, soluble intercellular adhesion molecule-1 and von Willebrand factor

B. Materson, R. Preston, A. Alonso, 2002, Journal of hypertension.

Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: a prospective, multicenter study.

P. Mannucci, C. Kessler, B. Ewenstein, 2002, Blood.

Elevated platelet P-selectin expression and platelet activation in high risk patients with uncontrolled severe hypertension.

B. Materson, R. Preston, A. Alonso, 2007, Atherosclerosis.

Multisite study for genotyping of the factor II (prothrombin) G20210A mutation by the invader assay.

M. Hessner, K. Voelkerding, K. Friedman, 2001, Clinical chemistry.

A multi-site study for detection of the factor V (Leiden) mutation from genomic DNA using a homogeneous invader microtiter plate fluorescence resonance energy transfer (FRET) assay.

M. Hessner, R. Larson, K. Friedman, 2000, The Journal of molecular diagnostics : JMD.

Early injection of high-dose recombinant factor VIIa decreases blood loss and prolongs time from injury to death in experimental liver injury.

J. Macleod, S. Cohn, M. Lynn, 2002, Journal of Trauma.

A Comparative Study of Three Methods for the Visualization of von Willebrand Factor (vWF) Multimers

F. Civantos, M. Ledford, J. Kent, 1990, Thrombosis and Haemostasis.

Efficacy of danazol in a patient with congenital protein-S deficiency: paradoxical evidence for decreased platelet activation with increased thrombin generation.

M. Brito, A. Horton, M. Ledford, 1997, Thrombosis research.

Chemotherapy‐induced hemolytic uremic syndrome: Description of a potential animal model

C. Hillyer, H. McClure, T. Barrett, 1995, Journal of medical primatology.

Familial Infantile Thrombotic Thrombocytopenic Purpura

J. Moake, J. Jimenez, A. Yunis, 1996, Journal of pediatric hematology/oncology.

Severe protein S deficiency in a newborn.

C. Pegelow, G. Zilleruelo, J. Young, 1992, Pediatrics.

Homzygous Protein S Deficiency due to a One Base Pair Deletion that Leads to a Stop Codon in Exon III of the Protein S Gene

P. Reitsma, C. Pegelow, R. Bertina, 1994, Thrombosis and Haemostasis.

New variant of von Willebrand disease type II with markedly increased levels of von Willebrand factor antigen and dominant mode of inheritance: von Willebrand disease type IIC Miami.

I. Rabinowitz, F. Civantos, J. Sadler, 1993, Blood.

Detection of genomic polymorphisms associated with venous thrombosis using the invader biplex assay.

M. Hessner, T. Williams, E. Lau, 2004, The Journal of molecular diagnostics : JMD.