Zobrazeno 1 - 10
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pro vyhledávání: '"Jenny McDade"'
Publikováno v:
Hematology Am Soc Hematol Educ Program
Cold-reactive autoimmune hemolytic anemia (AIHA) is rare among the hemolytic anemias. It results when 1 of a variety of processes causes the generation of immunoglobulin M (IgM) autoantibodies against endogenous erythrocytes, resulting in complement
Akademický článek
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Akademický článek
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Publikováno v:
Pediatric Blood & Cancer. 56:837-839
Autoimmune hemolytic anemia (AIHA) is characterized by the presence of autoantibodies, most frequently of the IgG isotype, directed against erythrocyte surface antigens. The direct antiglobulin test (DAT) is the critical laboratory test for the diagn
Publikováno v:
Peabody Journal of Education. 75:99-114
For the past 7 years, Springfield College (Springfield, MA) has reinvigorated attempts within the divisions of academic and student affairs to develop collaborative efforts with the Springfield Public Schools and the neighborhoods that are adjacent t
Publikováno v:
Pediatric bloodcancer. 56(5)
Autoimmune hemolytic anemia (AIHA) is characterized by the presence of autoantibodies, most frequently of the IgG isotype, directed against erythrocyte surface antigens. The direct antiglobulin test (DAT) is the critical laboratory test for the diagn
Publikováno v:
The Journal of pediatrics. 156(1)
Loxosceles reclusa (brown recluse spider) bites often cause local envenomation reactions; however, acute hemolysis from systemic loxoscelism is rare. To highlight this important diagnostic consideration for unexplained hemolysis in areas endemic for
Publikováno v:
Pediatric bloodcancer. 51(6)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an important cause of hemolytic anemia worldwide. Severely affected patients have chronic hemolysis with exacerbations following oxidative stress. Mutations causing severe chronic non-spherocytic
Autor:
Patrick T. McGann, Jenny McDade
Publikováno v:
The Journal of Pediatrics. 159:69
Autor:
Jonathan M. Flanagan, Song Wu, Russell E. Ware, Banu Aygun, Amy Cone, Matthew P. Smeltzer, Nicole A. Mortier, Jenny McDade, Jane S. Hankins, Thad A. Howard
Publikováno v:
Blood. 114:820-820
Abstract 820 Introduction: Hydroxyurea therapy has proven laboratory and clinical efficacy for ameliorating the signs and symptoms of sickle cell anemia, primarily by increasing the level of fetal hemoglobin (HbF). Virtually all treated pediatric pat