Results 101 to 110 of about 11,080 (216)

Association Between Obesity Status and Hypertension Phenotypes: Are Inflammatory Indicators the Missing Link? Evidence From a Large Population Study

open access: yesThe Journal of Clinical Hypertension, Volume 28, Issue 4, April 2026.
ABSTRACT Hypertension exhibits variability in diagnosis and treatment across phenotypes. Obesity and metabolic disorders are key risk factors, interacting with inflammatory states. This study explores their associations with hypertension phenotypes and the mediating role of inflammation.
Xue Li   +4 more
wiley   +1 more source

Case Report: A rare form of congenital erythrocytosis due to SLC30A10 biallelic variants—differential diagnosis and recommendation for biochemical and genetic screening

open access: yesFrontiers in Pediatrics
Congenital erythrocytosis recognizes heterogeneous genetic basis and despite the use of NGS technologies, more than 50% of cases are still classified as idiopathic.
Rosalinda Giannini   +14 more
doaj   +1 more source

Male, Female, Other: Transgender and the Impact in Primary Care [PDF]

open access: yes, 2016
Transgender includes patients at various stages of their journey. It is important that providers care for transgender patients with a culturally sensitive approach, awareness, and competent skill. There are new terms to learn.
Markwick, Laura
core   +2 more sources

Maternal erythrocytosis as a risk factor for small for gestational age at term in high altitude [PDF]

open access: yesRevista Brasileira de Ginecologia e Obstetrícia
Objective To determine if maternal erythrocytosis is a risk factor for small-for-gestational age at term at 3,400-m altitude in pregnant women without intercurrent disease.
Wilfredo Villamonte-Calanche   +6 more
doaj   +1 more source

Macrophages support pathological erythropoiesis in Polycythemia Vera and Beta-Thalassemia [PDF]

open access: yes, 2014
Regulation of erythropoiesis is achieved by integration of distinct signals. Among these, macrophages are emerging as erythropoietin-complementary regulators of erythroid development, particularly under stress conditions. We investigated the contribution
Abdel-Wahab, Omar   +15 more
core   +1 more source

CHARACTERISTICS OF DIAGNOSTIC APPROACH TO ERYTHROCYTOSIS OF DIFFERENT GENESIS

open access: yesТерапевтический архив, 2012
Aim. To show distribution of the investigated patients into diagnostic groups, find out the diagnostic value of the levels of hemoglobin and packed cell volume as possible markers of absolute erythrocytosis in the group of patients with polycythaemia ...
M A Sokolova   +9 more
doaj  

Evaluating the Epidemiology and Management of Bovine Congestive Heart Failure [PDF]

open access: yes, 2019
A form of congestive heart failure is increasingly reported as a cause of death in feedlot cattle located at moderate altitude (≤ 1524 m.). Significant knowledge gaps exist in the epidemiology and management of this form of bovine congestive heart ...
Bassett, Adam
core   +1 more source

Isolated erythrocytosis: study of 67 patients and identification of three novel germ-line mutations in the prolyl hydroxylase domain protein 2 (PHD2) gene

open access: yesHaematologica, 2012
The oxygen sensing pathway modulates erythropoietin expression. In normal cells, intracellular oxygen tensions are directly sensed by prolyl hydroxylase domain (PHD)-containing proteins.
Elena Albiero   +6 more
doaj   +1 more source

Heterozygous Hemoglobin Sherwood Forest Causing Polycythemia

open access: yesCase Reports in Hematology, 2017
Hemoglobin (Hb) Sherwood Forest is a rare high-affinity hemoglobin first described in 1977, arising from an Arg to Thr substitution at codon 104 of the beta chain.
Vikram M. Raghunathan   +2 more
doaj   +1 more source

Erythrocytosis: Diagnosis and investigation

open access: yesInternational Journal of Laboratory Hematology
AbstractAn absolute erythrocytosis is present when the red cell mass is greater than 125% of the predicted. This is suspected when the hemoglobin or hematocrit is above the normal range. An erythrocytosis can be classified as primary or secondary and congenital or acquired. The commonest primary acquired disorder is polycythemia vera.
Iman Noumani   +2 more
openaire   +4 more sources

Home - About - Disclaimer - Privacy