Results 61 to 70 of about 7,491 (237)

Acquired pure megakaryocytic aplasia successfully treated with cyclosporine [PDF]

open access: yes, 2010
Acquired pure megakaryocytic aplasia is a rare hematological disorder characterized by thrombocytopenia with absent or markedly reduced megakaryocytes in the bone marrow.
Aisha Al Khinji   +8 more
core   +2 more sources

Erythropoiesis in health and disease: Distinguishing defective and ineffective erythropoiesis

open access: yesHemaSphere, Volume 10, Issue 1, January 2026.
Abstract Erythropoiesis is a finely regulated process ensuring continuous red blood cell production to maintain oxygen delivery. Disruptions in this process give rise to defective erythropoiesis, characterized by impaired lineage commitment and progenitor development, and ineffective erythropoiesis (IE), marked by expansion of erythroid progenitors ...
Sara El Hoss   +3 more
wiley   +1 more source

Blood markers of alcohol use in epistaxis patients [PDF]

open access: yes, 2018
Epistaxis and alcohol overconsumption are frequently encountered in patients admitted to emergency wards. The aim of the study was to analyze indirect markers of alcohol overconsumption in epistaxis patients and evaluate its role as a risk factor.
Holzmann, David   +2 more
core  

Mechanism of induction of anisocytosis [PDF]

open access: yes, 1965
The mechanism of induction of anisocytosis was studied with experimental anemia of rabbits induced by blood depletion and phenylhydrazine chloride injection.
Asakura, Hikaru
core   +1 more source

Deoxyuridine suppression test: a comparison of two methods and effect of thymidine on the incorporation of 3H-deoxyuridine into DNA in human bone marrow cells [PDF]

open access: yes, 1977
Deoxyuridine suppression tests have been performed by two different methods of six normoblastic and eight megaloblastic marrows. A good correlation was obtained between the results by the modified and the original methods. The simplified method was found
Chanarin, Israel   +2 more
core   +1 more source

Anemia and hematinic deficiencies in gastric parietal cell antibody-positive and antibody-negative erosive oral lichen planus patients with thyroid antibody positivity

open access: yesJournal of the Formosan Medical Association, 2016
Serum gastric parietal cell antibody (GPCA), thyroglobulin antibody (TGA), and thyroid microsomal antibody (TMA) are found in some erosive oral lichen planus (EOLP) patients.
Julia Y.-F. Chang   +5 more
doaj   +1 more source

Exploring low haemoglobin density as a no‐added‐cost screening marker to assess iron deficiency

open access: yesVox Sanguinis, Volume 121, Issue 1, Page 35-42, January 2026.
Abstract Background and Objectives Iron deficiency (ID), with or without anaemia, affects over 1 billion people globally. Early detection is essential, but current diagnostic tools may be costly, logistically complex and not widely accessible. This study evaluates low haemoglobin density percentage (LHD%), derived from mean corpuscular haemoglobin ...
Jesse Qiao, Sherif Rezk, Gagan Mathur
wiley   +1 more source

Effectiveness of blood transfusions and risk factors for mortality in children aged from 1 month to 4 years at the Bon Marche Hospital, Bunia, Democratic Republic of Congo [PDF]

open access: yes, 2012
Objective  To assess the effectiveness of blood transfusions in a hospital of north-eastern Democratic Republic of the Congo. Methods  Prospective study of children admitted for severe anaemia.
Akech   +9 more
core   +2 more sources

Monitoring Variant Allele Fraction in VEXAS Syndrome: A Comparison of Digital PCR and Next‐Generation Sequencing

open access: yeseJHaem, Volume 6, Issue 6, December 2025.
ABSTRACT Background VEXAS syndrome is an adult‐onset, X‐linked autoinflammatory disorder resulting from somatic variations in the UBA1 gene. Aim To evaluate the adequacy of the digital PCR (dPCR) to follow up the variant allele frequency (VAF) on response to the treatment in patients with VEXAS. Patient and Methods This study is a 1‐year follow‐up of a
Alba Exposito‐Bey   +4 more
wiley   +1 more source

A Case of Subacute Combined Degeneration of Spinal Cord Diagnosed by Vitamin B12 Administration Lowering Methylmalonic Acid

open access: yesCase Reports in Neurology, 2020
Subacute combined degeneration of the spinal cord (SCDS) is a neurodegenerative disease characterized by subacute progression in the central and peripheral nervous systems mainly caused by vitamin B12 deficiency.
Daisuke Hara   +6 more
doaj   +1 more source

Home - About - Disclaimer - Privacy