Results 11 to 20 of about 78,012 (285)

Abnormal erythrocyte metabolism in hepatic disease [PDF]

open access: yesBlood, 1975
Abstract Erythrocyte (RBC) metabolic studies were done on 114 patients with severe hepatic disease. Heinz body formation after incubation of RBCs with acetyl phenylhydrazine was found to be significantly higher in patients than in controls.
J R, Smith   +3 more
openaire   +3 more sources

Erythrocytes of the Rhesus and Cynomolgus Monkeys

open access: yesEuropean Journal of Histochemistry, 2019
The monograph Erythrocytes of the Rhesus and Cynomolgus Monkeys is devoted to the cytologic, quantitative, generative normal and abnormal presentations of the erythrocytes in these two species of primates...
Vincenzo Stingo
doaj   +1 more source

Microscopic Studies on Erythrocytes of Channa punctata Exposed to Commercial Grade Lindane

open access: yesBrazilian Archives of Biology and Technology, 2018
Light and scanning electron microscopic studies of erythrocytes of Channa punctata exposed to two sublethal doses of lindane over a period of 21 days revealed myriads of anomalies. High frequency of micronucleus appeared progressively in the erythrocyte,
Debasish Bhattacharjee, Suchismita Das
doaj   +1 more source

Erythrocytic Abnormalities in Experimental Malaria.

open access: yesExperimental Biology and Medicine, 1967
SummaryStudies of erythroeytic indices and osmotic response revealed the presence of 2 abnormal populations of cells in hamsters infected with Plasmodium bergkei. One population consisted of mature nonpar asitized cells which became abnormally small and spherocytic with a diminished cellular surface area.
J N, George   +4 more
openaire   +2 more sources

Abdominal magnetic resonance imaging examination of Tibetan patients with abnormal iron metabolism and a preliminary study of correlations with blood cell analysis

open access: yesJournal of International Medical Research, 2020
Objective The objective was to investigate factors influencing the high incidence of abnormal iron metabolism in a Tibetan population. Methods This was a retrospective observational study.
Yi Zhou   +9 more
doaj   +1 more source

Validation and determination of a reference interval for Canine HbA1c using an immunoturbidimetric assay [PDF]

open access: yes, 2017
Background: Hemoglobin A1c (HbA1c) provides a reliable measure of glycemic control over 2–3 months in human diabetes mellitus. In dogs, presence of HbA1c has been demonstrated, but there are no validated commercial assays. Objective: The purpose
Goemans, Anne F.   +2 more
core   +1 more source

Abnormal fatty acid composition of erythrocyte glycosphingolipids in congenital dyserythropoietic anemia type II.

open access: yesJournal of Lipid Research, 1985
Glycosphingolipids were isolated from the erythrocytes of three siblings clinically affected with congenital dyserythropoietic anemia type II (CDA-II) as well as from the erythrocytes of their parents and of normal individuals.
J F Bouhours, D Bouhours, J Delaunay
doaj   +1 more source

Oxidative stress in the pathogenesis of systemic scleroderma: An overview [PDF]

open access: yes, 2018
Systemic sclerosis (SSc) is a rare disorder of the connective tissue characterized by fibrosis of the skin, skeletal muscles and visceral organs. Additional manifestations include activation of the immune system and vascular injury. SSc causes disability
Gambardella, Lucrezia   +5 more
core   +1 more source

Sickle Cell Anaemia with Antiglobulin Positive Autoimmune Haemolytic Crisis [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2023
Dear Editor, Immune-mediated haemolytic crises can worsen congenital anemias, and although autoantibodies have been identified, they are not frequently associated with overt Autoimmune Haemolytic Anaemia (AIHA) [1].
Saniya Khan   +3 more
doaj   +1 more source

Abnormalities of the Erythrocyte Membrane [PDF]

open access: yesPediatric Clinics of North America, 2013
Primary abnormalities of the erythrocyte membrane are characterized by clinical, laboratory, and genetic heterogeneity. Among this group, hereditary spherocytosis patients are more likely to experience symptomatic anemia. Treatment of hereditary spherocytosis with splenectomy is curative in most patients.
openaire   +2 more sources

Home - About - Disclaimer - Privacy