Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ronald S. Weinger"'
Publikováno v:
American Journal of Hematology. 87:413-416
Publikováno v:
Blood. 55:811-816
A 72-yr-old male with a lifelong history of easy bruisability and posttraumatic bleeding had a prolonged prothrombin time and activated partial thromboplastin time. His plasma Stypven, Taipan, and Echis carinatus venom clotting times were prolonged.
Publikováno v:
American Journal of Hematology. 9:237-248
A 38-year-old male patient with a life-long history of easy bruising and mild bleeding had a prolonged activated partial thromboplastin time (APTT), prothrombin time (PT), and thrombin time (TT). Reptilase (Bathrops atrox) clotting time was normal. H
Publikováno v:
American journal of hematology. 6(2)
Eleven patients with heparin-induced thrombocytopenia were studied. Thrombocytopenia appeared 3-16 days following the initiation of prophylactic or therapeutic doses of heparin. The mean lowest platelet count recorded was 48,000/mm3. When heparin was
Publikováno v:
American journal of diseases of children (1960). 134(8)
von Willebrand's disease (vWD) is an inherited disorder of bleeding, which is characterized by easy bruisability, mucosal hemorrhages, excessive posttraumatic bleeding, prolonged skin bleeding times, and quantitative or qualitative defects of the fac
Publikováno v:
American journal of hematology. 3
Eleven days after administration of multiple penicillin analogs, a 55-year-old female developed a Coombs-positive hemolytic anemia. The patient's erythrocytes were coated with IgG, complement components (C4/C3) and her serum contained elevated 125I-C
Autor:
Ronald S. Weinger, Charleen M. Moore
Publikováno v:
American journal of hematology. 8(4)
An individual with normal male habitus, body proportions, and secondary sexual characteristics was admitted to the hospital with head trauma. A routine blood smear demonstrated that 36% of the granulocytes had "drumsticks". Chromosomal analysis revea
Publikováno v:
The Journal of urology. 122(1)
A case of recurrent gross hematuria, sickle cell trait and von Willebrand’s disease is reported. The gross hematuria abated promptly after the institution of cryoprecipitate therapy. The importance of considering von Willebrand’s disease in the d
Publikováno v:
Annals of internal medicine. 89(6)
Two families are described with members who have both von Willebrand's disease and telangiectasias. Family A has four members in three consecutive generations that have both von Willebrand's disease and telangiectasias. von Willebrand's disease in th
Publikováno v:
Annals of Internal Medicine. 94:47
A 16-year-old boy had IIB von Willebrand's disease. The disorder is characterized by prolonged bleeding times; normal plasma levels of factor VIII-coagulant activity, factor VIII-ristocetin cofactor activity, and factor VIII-related antigen; abnormal