Results 161 to 170 of about 8,414 (207)
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Familial Erythrocytosis

Scandinavian Journal of Haematology, 1979
Erythrocytosis was found in 3 generations of an English family. The red cell mass was only moderately increased in some of the affected members but was accompanied by an unusually low plasma volume. Oxygen affinity of Hb was normal. Changes in serum and urinary erythropoietin showed an essentially normal pattern throughout a series of venesections ...
C, Howarth   +3 more
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Erythrocytosis in Emphysema

British Journal of Haematology, 1963
Marked erythrocytosis is frequently seen in hypoxia due to high altitudes and cyanotic congenital heart disease (Hurtado, Merino and Delgado, 1945) but is relatively uncommon in association with chronic respiratory failure (Baldwin, Cournand and Richards, 1949). This discrepancy has exercised a number of writers.
B J, FREEDMAN, D G, PENINGTON
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Thyrotoxic Erythrocytosis

Southern Medical Journal, 1982
Erythrocytosis in a woman with hyperthyroidism prompted evaluation for other causes of an elevated hematocrit level. No underlying cause was identified, and the erythrocytosis resolved as the thyroid status returned to normal. The possibility of thyrotoxicosis should be considered in a patient with an elevated hematocrit value.
A, Khojasteh, M C, Perry
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Primary Familial Erythrocytosis

Archives of Pediatrics & Adolescent Medicine, 1967
PRIMARY erythrocytosis or "benign familial polycythemia" is characterized by an increase in the hemoglobin concentration and the red blood cell count (RBC) due to an increase in total circulating red cell mass. The disease occurs in a familial pattern, is seen primarily in children, and follows a relatively benign course.
S B, Kontras, C, Romshe
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Polycythemia: Erythrocytosis and Erythremia

Annals of Internal Medicine, 1968
Abstract A classification of polycythemia and three cases of demonstrating increased red cell mass are presented.
WILLIAM N. VALENTINE   +9 more
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Erythrocytosis and Wilms' Tumour

Scandinavian Journal of Haematology, 1978
A Wilms' tumour was diagnosed in an 18‐year‐old male patient with erythrocytosis. After radical excision of the tumour and postoperative irradiation and chemotherapy, the erythrocytosis disappeared and did not recur during a 2‐year observation period. The levels of erythropoiesis‐stimulating activity in serum and in the renal mass suggest the tumour as
P H, Slee   +3 more
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The HIF Pathway and Erythrocytosis

Annual Review of Pathology: Mechanisms of Disease, 2011
Because of the central role that red blood cells play in the delivery of oxygen to tissues of the body, red blood cell mass must be controlled at precise levels. The glycoprotein hormone erythropoietin (EPO) regulates red blood cell mass. EPO transcription, in turn, is regulated by a distinctive oxygen-sensing mechanism.
Frank S, Lee, Melanie J, Percy
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Erythrocytosis

Abstract This chapter guides the reader on the diagnosis and management of erythrocytosis in hospitalized patients.
Diana De Oliveira, Gustavo Rivero
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Bartter's syndrome and erythrocytosis

The American Journal of Medicine, 1973
Abstract We describe a patient, known since 1960, with Bartter's syndrome and erythrocytosis. The diagnosis was made on the basis of hypokalemic alkalosis, hyperplasia of the juxtaglomerular apparatus, resistance to the presser effect of angiotensin, extremely high plasma renin activity and normal blood pressure.
D W, Erkelens, L W, Statius van Eps
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Smoking as a Cause of Erythrocytosis

Annals of Internal Medicine, 1975
Five smokers had erythrocyte masses sufficiently larger than normal to pose a problem in the differential diagnosis of polycythemia. Evaluation excluded lung disease, shunt physiology, hemoglobin with increased oxygen affinity, erythropoietin-producing tumor, renal disease, or polycythemia rubra vera as the primary cause of erythrocytosis in these ...
A L, Sagone, S P, Balcerzak
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