Results 81 to 90 of about 1,080,266 (216)

Plasma Exchange for Hantavirus Pulmonary Syndrome: A Mechanistic Case for an Untested Intervention

open access: yesJournal of Clinical Apheresis, Volume 41, Issue 5, October 2026.
ABSTRACT Hantavirus pulmonary syndrome (HPS) carries a case fatality rate of 35%–40% and has no approved pharmacologic treatment. Its pathophysiology is rooted in the plasma compartment: cytokines, viral antigens, immune complexes, and platelet‐binding glycoproteins circulate as drivers of immunopathologic endothelial injury, noncardiogenic pulmonary ...
Menatalla Nadim   +2 more
wiley   +1 more source

Diagnosis of immune thrombocytopenic purpura in children

open access: yes, 2007
Purpose of review This review updates the differential diagnosis between inherited and acquired immune thrombocytopenic purpura. as well as clinical practice on the initial diagnosis of children with the disease.
Geddis, Ae, BALDUINI, CARLO
core   +1 more source

Severe Thrombocytopenia Associated With Glucagon‐Like‐1 Receptor Agonists (GPL‐1RA): A SONAR Report

open access: yes
Diabetes, Obesity and Metabolism, EarlyView.
Charles L. Bennett   +15 more
wiley   +1 more source

Dispensing Patterns of Influenza and Pneumococcal Vaccines in the Private Healthcare Sector in South Africa for 2017 to 2021: A Longitudinal Study

open access: yesPharmacoepidemiology and Drug Safety, Volume 35, Issue 10, October 2026.
ABSTRACT Purpose The primary aim was to conduct a longitudinal pharmacoepidemiological study on the dispensing patterns of the influenza and pneumococcal vaccines in a section of the private healthcare sector in South Africa in the presence of the COVID‐19 vaccine to document the dispensing of these two respiratory vaccines alongside COVID‐19 vaccines.
I. Truter   +4 more
wiley   +1 more source

Prevalence of Immune Thrombocytopenia Purpura in Wasit Province

open access: yesWasit Journal for Pure Sciences
A lower than normal platelet count is a hallmark of the acquired autoimmune disease immune thrombocytopenic purpura (ITP). This autoimmune disease is characterized by low platelet counts, purpura, and hemorrhagic episodes caused by antiplatelet ...
Rawan Alaa
doaj   +1 more source

Beyond the Kidney and Lung: Cutaneous and Mucosal Clues to Human Hantavirus Disease

open access: yesInternational Journal of Dermatology, Volume 65, Issue 10, Page 2018-2027, October 2026.
Rodent exposure and aerosolized excreta can lead to hantavirus infection with systemic endothelial injury and capillary leak, resulting in thrombocytopenia and syndromes such as HPS/HCPS and HFRS/NE. Early dermatologic and mucosal findings, including flushing, conjunctival injection, petechiae/purpura, and mucosal bleeding, may provide important clues ...
Giuseppe Gallo   +2 more
wiley   +1 more source

Current management of thrombotic thrombocytopenic purpura

open access: yes, 2008
PURPOSE OF REVIEW: New treatment modalities have become increasingly popular for the treatment of acute thrombotic thrombocytopenic purpura. Widespread availability of ADAMTS13 assays resulted in the increased recognition of patients with hereditary ...
Kremer Hovinga, Johanna A, Meyer, Sara C
core   +1 more source

Evaluation of Reticulin Fibrosis in Benign Hematologic Disorders in Lahore, Pakistan: A Cross-Sectional Study

open access: yesLife and Science
Objective: To assess reticulin fibrosis in benign hematologic disorders and to understand the impact of benign hematologic disorders on the immune system. Study Design: Cross-sectional study.
Yasir Shabbir   +5 more
doaj   +1 more source

Assessment of the Performance of Siemens Scopio Digital Morphology on Bone Marrow Aspirates in Onco‐Hematology

open access: yesInternational Journal of Laboratory Hematology, Volume 48, Issue 5, Page 1000-1007, October 2026.
ABSTRACT Objectives Digital morphology (DM) systems assisted by artificial intelligence are increasingly being introduced into hematology laboratories; however, data on their performance in routine clinical practice for bone marrow aspirates (BMA) remain limited.
Gina Zini   +6 more
wiley   +1 more source

Is It a Coincidence or Secondary Immune Thrombocytopenic Purpura? A Case of an 11-Year-Old Male Patient at Hawassa University Comprehensive Specialized Hospital, Hawassa, Sidama, Ethiopia

open access: yesInternational Medical Case Reports Journal, 2022
Worku Ketema,1 Kefyalew Taye,1 Negash Tagesse,1 Aberash Eifa2 1Department of Paediatrics and Child Health, Hawassa University Comprehensive Specialized Hospital, Hawassa, Ethiopia; 2Department of Midwifery, Hawassa University Comprehensive Specialized ...
Ketema W, Taye K, Tagesse N, Eifa A
doaj  

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