Zobrazeno 1 - 10
of 22
pro vyhledávání: '"J R, Eckman"'
Publikováno v:
Thrombosis and haemostasis. 85(6)
The effects of dietary n-3 fatty acids (n-3FAs) on the frequency of pain episodes and ex vivo blood tests of thrombosis have been evaluated in patients with sickle cell disease (SCD) utilizing a double-blind, olive oil-controlled clinical trial. Diet
Publikováno v:
American journal of hematology. 53(2)
Adherence of sickle erythrocytes to vascular endothelium likely initiates or participates in microvascular occlusion, leading to ischemic tissue and organ damage characteristic of sickle-cell pain episodes. In vitro, sickle-cell adherence to endothel
Autor:
M C, Walters, M, Patience, W, Leisenring, J R, Eckman, G R, Buchanan, Z R, Rogers, N E, Olivieri, E, Vichinsky, S C, Davies, W C, Mentzer, D, Powars, J P, Scott, F, Bernaudin, K, Ohene-Frempong, P J, Darbyshire, A, Wayne, I A, Roberts, P, Dinndorf, S, Brandalise, J E, Sanders, D C, Matthews, F R, Appelbaum, R, Storb, K M, Sullivan
Publikováno v:
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. 2(2)
While allogeneic marrow transplantation is curative therapy for patients with sickle cell anemia, only a small fraction of patients in the United States receive this treatment. We surveyed participants in our multicenter study of marrow transplantati
Publikováno v:
American journal of medical genetics. 62(1)
Thalassemias occur in individuals of all ethnic backgrounds and are among the most common genetic diseases worldwide. The diagnosis of thalassemia can easily be part of primary medical practice. Here we outline a practical approach to the detection o
Publikováno v:
Blood. 85(10)
Vaso-occlusive pain episodes in sickle cell anemia are hypothesized to be precipitated by adherence of sickle erythrocytes to vascular endothelium in the microcirculation. Febrile episodes, thought to be viral in etiology, are frequently associated w
Autor:
D L, Wethers, G M, Ramirez, M, Koshy, M H, Steinberg, G, Phillips, R S, Siegel, J R, Eckman, J T, Prchal
Publikováno v:
Blood. 84(6)
Leg ulcers are a chronic manifestation of sickle-cell disease (SCD) and are often painful, disabling, and difficult to treat. RGD peptide matrix treatment is a novel therapy designed to provide a topical synthetic extracellular matrix that can act as
Publikováno v:
Pediatrics. 93(3)
To compare laboratory and programmatic issues in neonatal hemoglobin screening in two systems using either liquid cord blood or heel puncture blood dried on filter paper (DB) to determine the accuracy of hemoglobin phenotype; the collection rate of c
Publikováno v:
Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists. 9(1)
Comparing sustained attention and inhibitory control among youth with sickle cell syndrome (SCS) and nondiseased sibling controls, this study found significant differences in multiple components of attention and inhibitory control as a function of ch
Publikováno v:
The Journal of laboratory and clinical medicine. 120(4)
Complications in sickle syndromes are thought to result from regional disturbances of normal blood flow with subsequent ischemic damage. Adherence of sickle erythrocytes has been implicated in the pathophysiology of occlusive complications. Most prev
Autor:
P. L. Verter, E. W. Dean, G. m. b. H. Mono, W. Steuer, E. Ott, L. S. Walters, P. Lebeau, P. Marmasse, null Siemens, A. G. Halske, J. Ŝvéda, A. Dobrjanski, W. H. Ross, H. L. Trumbull, K. Kling, G. G. Oberfell, S. D. Sbinkle, S. B. Meserve, A. M. Erskine, B. Hilliger, F. Krüger, O. Reinkober, H. Riegger, H. Deringer, E. Berl, K. Andress, L. Jordan, J. R. Eckman
Publikováno v:
Zeitschrift für Analytische Chemie. 76:456-463