Results 181 to 190 of about 722,667 (218)
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Plasma lipids in beta-thalassemia minor
Atherosclerosis, 1989Because total cholesterol levels have been found to be lower in patients affected by thalassemia major and intermedia, we examined the plasma lipid pattern of 628 beta-thalassemia trait carriers and 4552 controls in order to evaluate whether the plasma lipid impairment is also present in the heterozygous state.
M, Maioli +6 more
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[Arthritis in thalassemia minor].
Schweizerische medizinische Wochenschrift, 1977Seven cases with the syndrome of thalassemia minor and pauciarticular, non-erosive, seronegative arthritis are described. Other known causes of seronegative arthritis had been excluded. There was a predilection for middlesized joints such as ankles, wrists and elbows. Usually the synovitis was asymmetrical from onset, with one to eight joints affected.
U, Schlumpf +5 more
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Thalassemia Minor and Major: Current Management
The Indian Journal of Pediatrics, 2017Thalassemia is a common genetic disorder. It has been estimated that in India nearly 5 crore people are thalassemia carriers. They are asymptomatic and are detected on blood tests. These people are at same risk of developing iron deficiency anemia as general population and need iron therapy in the presence of iron deficiency anemia.
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Hemosiderosis in Association With Thalassemia Minor
Archives of Internal Medicine, 1968Iron deficiency anemia is by far the most common of the hypochromic microcytic anemias, but in recent years at least six other hypochromic syndromes have been described, the most common of which is thalassemia.1The thalassemia syndromes are being recognized more frequently, and it is now known that they occur commonly in Southern Asia and the Middle ...
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Antenatal screening for thalassemia minor.
Obstetrics and gynecology, 1988This report describes the findings of a screening program of 918 obstetric patients for thalassemia minor. Patients with erythrocyte mean corpuscular volume (MCV) less than 80 fL on initial complete blood count were evaluated with serum iron, total iron binding capacity, quantitative hemoglobin electrophoresis, and trial of iron replacement.
D L, Gehlbach, L L, Morgenstern
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[Arthropathy in beta-thalassemia minor].
Medizinische Klinik (Munich, Germany : 1983), 2000A 25-year-old Turkish patient presented with a "swelling" of the ankles which now persisted for 5 years. He had previously been diagnosed as having HLA-B27 negative spondylarthropathy with peripheral joint involvement. The symptoms failed to respond to different therapies.
J, Richter +3 more
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Tumors of the Major and Minor Salivary Glands
Ca-A Cancer Journal for Clinicians, 1984Robert J McKenna
exaly