Zobrazeno 1 - 10
of 56
pro vyhledávání: '"R E Ware"'
Publikováno v:
Irrigation and Drainage Systems. 14:93-120
A detailed Diagnostic Analysis (DA)was performed on an irrigation district in CentralArizona as part of a Management Improvement Program(MIP). The DA was conducted by an interdisciplinaryteam who focused their findings on performance of theirrigated
Autor:
Manjit Hanspal, Scott J. Yi, James Murray, S. S. Winter, Hani Hassoun, J. N. Vassiliadis, R. E. Ware, Jiri Palek, Shyh-Shin Chiou
Publikováno v:
Journal of Clinical Investigation. 96:2623-2629
We describe a spectrin variant characterized by a truncated beta chain and associated with hereditary spherocytosis. The clinical phenotype consists of a moderate hemolytic anemia with striking spherocytosis and mild spiculation of the red cells. We
Publikováno v:
The Journal of Immunology. 155:2407-2418
CD7 is a 40-kDa transmembrane glycoprotein member of the lg gene superfamily expressed on most peripheral blood T lymphocytes and NK cells. CD7 is also expressed on myeloid, NK, B, and T cell precursors during adult hematopoiesis. Because Thy-1 is ab
Autor:
R E, Ware, T A, Howard
Publikováno v:
Blood. 82:2137-2142
In an attempt to identify and characterize T-lymphocyte immunoregulatory abnormalities in immune thrombocytopenic purpura (ITP), we have performed phenotypic and clonal analysis on peripheral T lymphocytes from 23 children with ITP. Quantitation of l
Autor:
C D, Thornburg, R E, Ware
Publikováno v:
Clinical and laboratory haematology. 25(1)
Autohaemolysis testing can assist the evaluation of haemolytic anaemia, but involves a cumbersome assay that is difficult to perform accurately. Because this test persists in clinical practice without clear indications or guidelines, we retrospective
Autor:
A, Amalfitano, A R, Bengur, R P, Morse, J M, Majure, L E, Case, D L, Veerling, J, Mackey, P, Kishnani, W, Smith, A, McVie-Wylie, J A, Sullivan, G E, Hoganson, J A, Phillips, G B, Schaefer, J, Charrow, R E, Ware, E H, Bossen, Y T, Chen
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 3(2)
Infantile glycogen storage disease type II (GSD-II) is a fatal genetic muscle disorder caused by deficiency of acid alpha-glucosidase (GAA). The purpose of this study was to investigate the safety and efficacy of recombinant human GAA (rhGAA) enzyme
Publikováno v:
The Journal of rheumatology. 28(2)
Thrombophilia can result from either inherited or acquired conditions. We describe a teenager who developed extensive thrombosis requiring aggressive and prolonged anticoagulation. Laboratory evaluation revealed an acquired lupus anticoagulant, consi
Autor:
S A, Zimmerman, R E, Ware
Publikováno v:
Clinical and laboratory haematology. 22(3)
This study aimed to investigate the prevalence of palpable splenomegaly in children with haemoglobin SC (Hb SC) disease, and to determine the haematological and clinical manifestations of splenomegaly in this patient population. We performed a retros
Publikováno v:
The Journal of pediatrics. 136(6)
Glomerular disease and renal failure cause substantial morbidity for patients with sickle cell disease (SCD). Proteinuria is an early manifestation of sickle nephropathy, but the prevalence of proteinuria and its clinical correlations in children wit
Publikováno v:
Blood. 95(11)
Hydroxyurea (HU) is an effective therapeutic agent for patients with myeloproliferative disorders (MPDs) or sickle cell disease (SCD). Short-term HU toxicities primarily include transient myelosuppression, but long-term HU risks have not been defined