Results 161 to 170 of about 75,555 (208)
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Erythrocyte Abnormality Induced, by Protein Malnutrition
British Journal of Haematology, 1967SUMMARYRed cell survival studies using 51 Cr‐labelled erythrocytes were carried out on 14 subjects with protein malnutrition (12 kwashiorkor and two marasmus). The T½ varied from 3 to 20 days with a mean of 12.4 days. There was significant accumulation of radioactivity demonstrable on scanning over the liver and spleen in three kwashiorkor patients ...
P, Lanzkowsky +5 more
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Erythrocyte membrane skeleton abnormalities in hereditary spherocytosis
British Journal of Haematology, 1983Summary. Erythrocyte ghosts from eight individuals with hereditary spherocytosis have been compared with respect to their protein compositions as judged by SDS gel electrophoresis, their ease of spectrin extractability, and their freeze‐etch electron microscopic appearance after incubation in conditions designed to promote aggregation of the ...
B E, Burke, D M, Shotton
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Erythrocyte membrane abnormalities in sickle cell disease
Biotechnology and Applied Biochemistry, 1990A large fraction of circulating sickle red cells contain one or more large vesicles which are not found in normal erythrocytes. These vesicles contain very high levels of Ca2+, and probably account for the long‐known elevation of cellular Ca2+ in sickle cells. These vesicles contain the plasma membrane CaATPase and leak Ca2+ by a nitrendipine‐sensitive
P, Williamson +3 more
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Erythrocyte membrane abnormalities in human myotonic dystrophy
Journal of the Neurological Sciences, 1980Membrane-bound enzyme activities and cardiac glycoside binding were determined in red blood cell membrane preparations from patients with myotonic dystrophy and in age matched controls. Na+-K+-activated ATPase activity was significantly increased in myotonic patients.
S K, Mishra, M, Hobson, D, Desaiah
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Abnormal Erythrocyte Endothelial Adherence in Hereditary Stomatocytosis
Blood, 1997AbstractHereditary stomatocytosis is a red cell membrane protein disorder, which results in hemolytic anemia. Some patients with hereditary stomatocytosis experience dyspnea, chest pain, and abdominal pain, particularly after splenectomy. These symptoms may represent vaso-occlusion secondary to adherence of an abnormal erythrocyte membrane to vascular ...
B D, Smith, G B, Segel
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Abnormalities of erythrocytes in duchenne muscular dystrophy
Annals of Neurology, 1983AbstractErythrocytes from patients with Duchenne muscular dystrophy (DMD) were studied in relation to the extracellular calcium ion concentration. The shape of fresh erythrocytes in DMD was normal and not affected by Ca++. When DMD erythrocytes were stored in buffer solution with Ca++, however, the rate of the shape change over time was enhanced ...
M, Yoshida, K, Ando, E, Satoyoshi
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Abnormal erythrocyte survival in patients with myotonic dystrophy
Acta Neurologica Scandinavica, 2009In four of six patients with myotonic dystrophy whom we studied 51Cr labeled erythrocytes were found to have a biphasic survival kinetic. After in initial significantly more rapid disappearance than in controls, about 80% of the labeled cells reappeared in circulation, and were thereafter eliminated at a significantly faster rate than normal. This type
O, Sydow, H, Stibler, R, Hast
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Abnormal erythrocyte choline and influx in Alzheimer's disease
Life Sciences, 1986Choline transport and levels were studied in erythrocytes from patients with Alzheimer's disease and age-matched controls using stable isotopic tracer techniques. The mean erythrocyte choline in the Alzheimer group was 50.1 nmol ml-1 compared to 15.5 nmol ml-1 in the controls.
B L, Miller +5 more
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Erythrocyte enzyme abnormalities in leukemias.
The Journal of the Association of Physicians of India, 2006Red cell enzymes were assayed in a total of 67 patient including 24 patients with AML (19 relapse, 5 remission), 16 patients with ALL (10 relapse, 6 remission), 22 patients with CML and 5 patients with blastic CML. Diagnosis of leukemia was based on clinical presentation, peripheral blood smear and bone marrow examination (as per FAB classification ...
Subhadra, Sharma, H P, Pati
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[Erythrocyte membrane abnormalities - hereditary elliptocytosis].
Georgian medical news, 2016This study was designed to investigate the 4 year old boy with Hereditary Elliptocitosis (HE). The diagnosis of this rare hemolytic anemia was based on detailed family history (positive in the 4-th generation), physical examination and Para-clinical data analyses. The vast majority of patients with HE are asymptomatic, severe forms are rare.
M, Kvezereli-Kopadze +3 more
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