Results 171 to 180 of about 11,080 (216)
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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 and Hypernephroma

Scandinavian Journal of Haematology, 1964
The results of a study on the content of erythropoietic‐stimulating factor in the serum, urine and extracts from tumour tissue and normal renal tissue from a patient with erythrocytosis and hypernephroma of the left kidney are reported. Extracts from the solid parts of the tumour showed a high concentration of this factor. It seems reasonable to assume
E B, THORLING, J, ERSBAK
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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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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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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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SYMPTOMATIC ERYTHROCYTOSIS

Farmaciâ Kazahstana, 2021
В статье характеризуются основные виды, причины, ключевые звенья механизмов развития различных форм патологии в системе эритроцитов, их основные проявления и принципы устранения. The article describes the main types, causes, key links of the mechanisms of ...
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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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Fibromyomatous Erythrocytosis

New England Journal of Medicine, 1962
E D, ABOULAFIA   +2 more
openaire   +2 more sources

Primary erythrocytosis

The Journal of Pediatrics, 1963
C F, ABILDGAARD   +2 more
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Lenvatinib-Associated Erythrocytosis

American Journal of Therapeutics, 2023
Rachaita, Lakra   +2 more
openaire   +2 more sources

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