Results 161 to 170 of about 7,240 (211)
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Secondary erythrocytosis

Expert Review of Hematology, 2023
Erythrocytosis is associated with an elevation of the hemoglobin level above 16.5 g/dL in men and above 16 g/dL in women and an elevation of the hematocrit level above 49% in men and > 48% in women. In primary erythrocytosis, the defect is a clonal disorder in the myeloid compartment of the bone marrow, leading to an increased red cell production ...
Rodrick Babakhanlou   +2 more
exaly   +3 more sources

Genetic Background of Congenital Erythrocytosis [PDF]

open access: yesGenes, 2021
True erythrocytosis is present when the red cell mass is greater than 125% of predicted sex and body mass, which is reflected by elevated hemoglobin and hematocrit. Erythrocytosis can be primary or secondary and congenital or acquired. Congenital defects
Mary Frances Mcmullin   +1 more
exaly   +2 more sources

NGS Evaluation of a Bernese Cohort of Unexplained Erythrocytosis Patients [PDF]

open access: yesGenes, 2021
: (1) Background: Clinical and molecular data on patients with unexplained erythrocytosis is sparse. We aimed to analyze the clinical and molecular features of patients with congenital erythrocytosis in our tertiary reference center.
Naomi A Porret   +2 more
exaly   +3 more sources

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
openaire   +3 more sources

Benign Erythrocytosis

British Journal of Haematology, 1968
Summary. Data obtained in the course of a previously reported study have been used to re‐emphasize the existence of a distinct clinical entity—benign erythrocytosis—often misdiagnosed as polycythaemia Vera.It has been demonstrated that, in contrast to PV, there is involvement of the red‐cell line only: neither leucocytosis, thrombocytosis nor ...
B, Modan, M, Modan
openaire   +2 more sources

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
openaire   +2 more sources

Diagnosis and management of congenital and idiopathic erythrocytosis [PDF]

open access: yesTherapeutic Advances in Hematology, 2012
An erythrocytosis occurs when there is an increased red-cell mass. The causes of erythrocytosis are divided into primary, when there is an intrinsic defect in the erythroid cell, and secondary, when the cause is extrinsic to the erythroid cell.
Mary Frances Mcmullin
exaly   +2 more sources

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
openaire   +2 more sources

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
openaire   +2 more sources

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