Results 191 to 200 of about 4,949,451 (244)
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Echocardiographic findings in thalassemia major
Acta Paediatrica, 1994[No abstract available]
Kilinc Y. +4 more
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Pancreatic Sonography in Thalassemia Major
Klinische Pädiatrie, 1983Four patients with thalassemia major and well documented transfusional anamnesis were investigated sonographically. Beside the fibrous reaction of iron overload in the liver the outstanding finding was the grossly increased echogenicity of the normal sized fibrotic pancreas in transfusional hemosiderosis.
R, Erttmann, G, Hausdorf, G, Landbeck
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Cardiac complications in thalassemia major
Annals of the New York Academy of Sciences, 2016The myocardium is particularly susceptible to complications from iron loading in thalassemia major. In the first years of life, severe anemia leads to high‐output cardiac failure and death if not treated. The necessary supportive blood transfusions create loading of iron that cannot be naturally excreted, and this iron accumulates within tissues ...
Auger, D, Pennell, DJ
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[Osteodystrophy in thalassemia major].
Annali italiani di medicina interna : organo ufficiale della Societa italiana di medicina interna, 1993Subjects with thalassemia major frequently have bone disorders of debatable pathogenesis. We attempt here to analyze the relationships between siderosis and thalassemic osteodystrophy by assessing calcium-phosphorus balance, hormone-vitamin homeostasis, osteoblastic-osteoclastic activity parameters, and bone mineral density (BMD) in 30 patients with ...
BISBOCCI, Daniela +7 more
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Pulmonary function in thalassemia major
The Journal of Pediatrics, 1987Pulmonary function tests were evaluated in 28 Chinese patients with beta-thalassemia major receiving regular transfusions and desferoxamine, and in 34 height-matched normal Chinese children. Comparison of lung function using analysis of covariance with reference to standing height showed that patients with thalassemia had a proportional decrease in ...
Fung, K.P. +3 more
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Psychosocial implications of Thalassemia Major
Pediatrics International, 2005Abstract Background : Many causes including the chronicity of disease, burden of treatment modalities, morbidities, and the expectation of early death resulting from the disease complications, may lead to psychosocial burden in Thalassemia Major ...
Aydinok Y. +4 more
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Myopathological Findings in Thalassemia Major
European Neurology, 2008In thalassemia major (TM) one third of patients suffers from muscle wasting, weakness and cramps. Six patients with TM were studied. All had muscle wasting and proximal weakness; serum levels of vitamin E were low (0.6–7.0 µg/dl) while CPK, LDH and aldolase were normal.
Y, Shapira +4 more
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Renal Enlargement in Thalassemia Major
Radiology, 1971Twenty-four patients with thalassemia major and no urinary tract complaints underwent excretory urography. The kidneys were large bilaterally in 17 patients; 2 other patients had enlargement of the left kidney. The autopsies of 13 patients were reviewed; the kidneys were large in all 13.
H, Grossman +3 more
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Endocrine Function in Thalassemia Major
The Journal of Clinical Endocrinology & Metabolism, 1968Abstract Seven patients with thalassemia major, ranging in age from 6½ to 23 yr, were studied. Growth retardation was present in all except the youngest patient. Thyroid and adrenal function was normal. Three patients, however, showed an unexplained increase in the serum protein bound iodine level.
B, Kuo, E, Zaino, M S, Roginsky
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Complications of thalassemia major and their treatment
Expert Review of Hematology, 2011The life of patients with thalassemia has improved both in duration and in quality in industrialized countries. Complications are still common and include heart disease (heart failure and arrhythmias), chronic liver hepatitis, which can evolve in cirrhosis and, rarely, in hepatocellular carcinoma, endocrine problems (hypogonadism, hypothyroidism ...
BORGNA, Caterina, M. R. Gamberini
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