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Thrombosis Research|November 1, 1984
Platelet factor 4 does not promote von Willebrand factor binding to human plateletsS P Levine, J L MoakeClinical Laboratory Science : Journal of the American Society for Medical Technology|May 27, 1999
von Willebrand factor in the pathophysiology of thrombotic thrombocytopenic purpuraJ L MoakeClinics in Haematology|May 1, 1986
Thrombotic thrombocytopenic purpura and the haemolytic-uraemic syndrome: evolving concepts of pathogenesis and therapyJ J Byrnes, J L MoakeCurrent Opinion in Pediatrics|February 17, 2000
Thrombotic thrombocytopenic purpura and the hemolytic-uremic syndromeK R Baker, J L MoakeThe American Journal of the Medical Sciences|August 15, 1998
Thrombotic thrombocytopenic purpura: understanding a disease no longer rareJ L Moake, T W ChowJournal of Clinical Apheresis|November 25, 1998
Increased von Willebrand factor (vWf) binding to platelets associated with impaired vWf breakdown in thrombotic thrombocytopenic purpuraJ L Moake, T W ChowThe American Journal of Medicine|September 1, 1989
Abnormalities of von Willebrand factor multimers in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndromeJ L Moake, P D McPhersonThe American Journal of Medicine|September 1, 1976
Sickle cell--betao thalassemia variant with high hemoglobin F and mild clinical courseJ R Shaeffer, J L MoakePageof 18