Results 151 to 160 of about 286,944 (278)

Monocyte count is a thrombosis marker: a pilot study.

open access: yes, 2014
This prospective case-control study suggests that monocyte value is both an easy and useful thrombosis criterion: the value above 500 cells/mm3 correlates with thrombosis at the onset and the value below 400 cells/mm3 correlates with restoration of ...
De Faveri U   +7 more
core  

Liver Transplantation Despite Active Intracranial Hemorrhage in Acetaminophen‐Induced Acute Liver Failure: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Acute liver failure with intracranial hemorrhage poses difficult transplant decisions. We report acetaminophen‐induced acute liver failure with cerebral edema and active multifocal hemorrhage successfully managed with emergent liver transplantation and staged neurosurgical intervention.
Daryna Shnitser   +3 more
wiley   +1 more source

Association of coagulation dysfunction with thrombosis, bleeding, and mortality in patients supported by veno–venous extracorporeal membrane oxygenation for viral pneumonia

open access: yes
Background Bleeding and thrombosis remain leading causes of morbidity and mortality in patients supported by extracorporeal membrane oxygenation (ECMO).
Ledot, Stephane   +10 more
core   +1 more source

Immune Thrombotic Thrombocytopenic Purpura Following Trimethoprim Sulfamethoxazole Reexposure: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT An 85‐year‐old man developed acute neurologic dysfunction, severe thrombocytopenia, microangiopathic hemolytic anemia, and ADAMTS13 activity of 4.6% after TMP‐SMX reexposure. Seven plasma‐exchange sessions plus corticosteroids produced rapid recovery.
Renee Morecroft   +6 more
wiley   +1 more source

JAK2 V617F mutation associated with cerebral venous thrombosis: a rare cause of intracranial hypertension

open access: yes, 2014
We present a case of cerebral venous thrombosis secondary to an unusual mutation, the Janus kinase 2 (JAK2 V617F) mutation. The patient complained of symptoms consistent with idiopathic intracranial hypertension (IIH).
Michelle Y. Wang; Peter A. Quiros
core  

Pregnancy Complicated by Hereditary Antithrombin Deficiency: A Case Study and Insights From the Literature

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT A pregnant woman with hereditary antithrombin deficiency was managed with adjusted‐dose LMWH throughout pregnancy, monitoring D‐dimer and anti‐Xa activity, successfully preventing thrombosis and hemorrhage.
Ya Zhao   +4 more
wiley   +1 more source

TTP‐Like Syndrome and Subsequent Non‐Aneurysmal Subarachnoid Hemorrhage in HbSC Disease: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Sickle cell disease (SCD) with hemoglobin‐ (Hb‐) SC genotype is often considered a milder SCD variant, yet life‐threatening complications can occur. A 26‐year‐old man with HbSC disease presented with an infection triggered vaso‐occlusive crisis (VOC), acute chest syndrome (ACS), severe thrombocytopenia, Coombs‐negative hemolysis with ...
Benjamin Vieten   +9 more
wiley   +1 more source

Unilateral thrombosis of dominant internal jugular vein presenting with benign intracranial hypertension

open access: yes
Benign intracranial hypertension (BIH) is defined as a chronic elevation of intracranial pressure (ICP) divided into primary, idiopathic intracranial hypertension, and secondary forms.
Kadir, Khairul Azmi Abd   +6 more
core  

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