Results 11 to 20 of about 28,854 (205)

Novel use Of Hydroxyurea in an African Region with Malaria (NOHARM): a trial for children with sickle cell anemia [PDF]

open access: yes, 2017
Hydroxyurea treatment is recommended for children with sickle cell anemia (SCA) living in high-resource malaria-free regions, but its safety and efficacy in malaria-endemic sub-Saharan Africa, where the greatest sickle-cell burden exists, remain unknown.
Hodges, James S.   +8 more
core   +2 more sources

Aqueous IR Bagendit rice leaf extract decreases reticulocyte count in lead-exposed rats

open access: yesUniversa Medicina, 2018
BACKGROUND Lead acetate may inhibit the enzyme aminolevulinate dehydratase (ALAD) resulting in decreased heme synthesis (and consequently in anemia) but in increased number of reticulocyte cells.
Budi Santosa   +2 more
doaj   +1 more source

Predicting response of severe aplastic anemia to immunosuppression combined with eltrombopag

open access: yesHaematologica, 2021
Pretreatment blood counts, particularly an absolute reticulocyte count ≥25×109/L, correlate with response to immunosuppressive therapy in severe aplastic anemia.
Yoshitaka Zaimoku   +6 more
doaj   +1 more source

CLINICAL UTILITY OF RETICULOCYTE INDICES IN THE DIAGNOSIS AND MANAGEMENT OF PAEDIATRIC SICKLE CELL DISEASE PATIENTS IN PORT HARCOURT, NIGERIA [PDF]

open access: yesSanamed
Introduction:Sickle cell anemia (SCA) is a hereditary blood disorder resulting from a point mutation in the β-globin gene, leading to the production of abnormal hemoglobin S that distorts red blood cell morphology and impairs their function. Reticulocyte
Jeremiah Zaccheaus   +3 more
doaj   +1 more source

Prognostic significance of endogenous erythropoietin in long-term outcome of patients with acute decompensated heart failure [PDF]

open access: yes, 2016
Aims Although previous reports suggest that an elevated endogenous erythropoietin (EPO) level is associated with worse clinical outcomes in chronic heart failure (HF) patients, the prognostic implication of EPO in patients with acute decompensated HF ...
Anand   +27 more
core   +1 more source

Pattern of hemolysis parameters and association with fetal hemoglobin in sickle cell anemia patients in steady state

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2015
Objective: This study aimed to evaluate the influence of fetal hemoglobin (Hb F) on hemolysis biomarkers in sickle cell anemia patients. Methods: Fifty adult sickle cell anemia patients were included in the study.
Juliane Almeida Moreira   +10 more
doaj   +1 more source

Clinical relevance of silent red blood cell autoantibodies. [PDF]

open access: yes, 2017
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Alessandri, C   +14 more
core   +1 more source

Overview of Anemia among Systemic Lupus Erythematosus Patients in Reproductive Age Women based on Reticulocyte Hemoglobin Equivalent (RET-He) Level and Reticulocyte Count

open access: yesIndonesian Journal of Rheumatology, 2018
Background: Anemia is a common manifestation found among patients with Systemic Lupus Erythematosus (SLE). It may be caused by iron-deficiency, autoimmune hemolytic, and chronic inflammation. Each anemia has different therapy approachments.
Ismiana Fatimah Modjaningrat   +3 more
doaj   +1 more source

THE ROLE OF ABSOLUTE RETICULOCYTE COUNTS IN EVALUATION OF PANCYTOPENIA: A CROSS-SECTIONAL STUDY, BIHAR, INDIA.

open access: yesStudent's Journal of Health Research Africa, 2023
Background Hematological conditions like pancytopenia are widespread in our lab. Diagnosis and therapy of pancytopenia require etiology analysis.
Rawi Agrawal   +3 more
doaj   +1 more source

Red Blood Cell Fragility and Reticulocyte Count in Hemolytic Anemic Patients with and Without G-6PD Enzyme Deficiency

open access: yesBangabandhu Sheikh Mujib Medical University Journal, 2010
Background: Erythrocyte G-6PD enzyme deficiency is an important cause of Hemolytic anemia with consequent increase in reticulocyte count. Objective: To assess the osmotic fragility of RBC status and reticulocyte count in G-6PD enzyme deficient patients ...
Monira Razzak   +2 more
doaj   +1 more source

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