Zobrazeno 1 - 10
of 45
pro vyhledávání: '"P F Milner"'
Publikováno v:
Quality Advancement in Nursing Education, Vol 1, Iss 2 (2015)
Externí odkaz:
https://doaj.org/article/f4740efc4b214b54ac2cfddec2df2e10
Autor:
M H, Steinberg, Z H, Lu, R L, Nagel, S, Venkataramani, P F, Milner, L, Huey, S, Safaya, R F, Rieder
Publikováno v:
American journal of hematology. 59(2)
To examine the effects of unusual or atypical beta-globin gene cluster haplotypes on the hematological features and Hb F levels of sickle cell anemia, we studied African Americans who had an atypical or Cameroon haplotype chromosome in association wi
Publikováno v:
American journal of hematology. 52(2)
Cardiac function was measured at rest and during exercise in 9 patients with sickle-cell anemia (SS) and coexisting homozygous alpha thalassemia-2 (alpha thal-2). Results were compared with 18 sickle cell patients with normal alpha globin genes, who
Autor:
P F, Milner, A P, Kraus, J I, Sebes, L A, Sleeper, K A, Dukes, S H, Embury, R, Bellevue, M, Koshy, J W, Moohr, J, Smith
Publikováno v:
Clinical orthopaedics and related research. (289)
The prevalence and incidence of osteonecrosis (ON) of the humeral head in sickle cell disease was determined by a study of 2524 patients who were entered into a prospective study and followed for an average of 5.6 years. At entry, 5.6% had roentgenog
Autor:
S, Charache, G J, Dover, R D, Moore, S, Eckert, S K, Ballas, M, Koshy, P F, Milner, E P, Orringer, G, Phillips, O S, Platt
Publikováno v:
Blood. 79(10)
Patients with sickle cell anemia were treated with daily doses of hydroxyurea, to assess pharmacokinetics, toxicity, and increase in fetal hemoglobin (Hb) production in response to the drug. Plasma hydroxyurea clearances were not a useful guide to ma
Publikováno v:
American Journal of Hematology. 1:283-292
The syndrome thalassemia intermedia can be the clinical expression of heterozygosity for different tyes of thalassemia, beta-thalassemia and hereditary persistence of fetal hemoglobin, beta-thalassemia and Hb-Lepore, and in blacks it may even represe
Publikováno v:
Blood. 63:64-72
Members of 7 large families, containing 20 patients with sickle cell anemia (SS) characterized by high levels of fetal hemoglobin (HbF), were studied using immunofluorescence to count F cells and a radioimmunoassay to measure small amounts of HbF. In
Publikováno v:
Southern Medical Journal. 78:1462-1469
We describe ten patients with sickle cell anemia who became acutely ill within a few days after a blood transfusion. Two patients died. In eight cases the posttransfusion detection of alloantibodies suggested that delayed hemolytic reactions to trans
Autor:
P. F. Milner
Publikováno v:
Archives of Internal Medicine. 133:565-572