<div><p>Background</p><p>The pathogenesis of development and rupture of intracranial aneurysms (IA) is largely unknown. Also, screening for IA to prevent aneurysmal subarachnoid hemorrhage (aSAH) is inefficient, as disease markers are lacking. We investigated gene expression profiles in blood of previous aSAH patients, who are still at risk for future IA, aiming to gain insight into the pathogenesis of IA and aSAH, and to make a first step towards improvement of aSAH risk prediction.</p><p>Methods and Results</p><p>We collected peripheral blood of 119 patients with aSAH at least two years prior, and 118 controls. We determined gene expression profiles using Illumina HumanHT-12v4 BeadChips. After quality control, we divided the dataset in a ...
Background and Purpose - Analyzing genes involved in development and rupture of intracranial aneurys...
Background: Recently, common genetic risk factors for intracranial aneurysm (IA) and aneurysmal suba...
Candidate gene studies have identified genetic variants associated with clinical outcomes following ...
The pathogenesis of development and rupture of intracranial aneurysms (IA) is largely unknown. Also,...
Background The pathogenesis of development and rupture of intracranial aneurysms (IA) is largely unk...
Purpose: Through comprehensive bioinformatics analysis based on the immune microenvironment, this st...
The rupture of an intracranial aneurysm (IA) causes devastating hemorrhagic strokes. Yet, most IAs r...
Subarachnoid hemorrhage (SAH) is a major cause of death and morbidity worldwide, often due to ruptur...
BackgroundThe rupture of an intracranial aneurysm (IA) causes devastating subarachnoid hemorrhages, ...
Peripheral blood mononuclear cells (PBMCs) play an important role in the inflammation that accompani...
Background: Ruptured intracranial aneurysm (IA) is a disease with high mortality. Despite the great ...
ABSTRACT Background: Subarachnoid haemorrhage is a devastating disease with high morbidity and morta...
OBJECTIVE: To gain comprehensive insight into the molecular mechanism of formation and rupture of in...
BackgroundIt is well known that ruptured intracranial aneurysms are associated with substantial morb...
We tried to identify molecular markers in peripheral blood to predict high risk of aneurysm rupture....
Background and Purpose - Analyzing genes involved in development and rupture of intracranial aneurys...
Background: Recently, common genetic risk factors for intracranial aneurysm (IA) and aneurysmal suba...
Candidate gene studies have identified genetic variants associated with clinical outcomes following ...
The pathogenesis of development and rupture of intracranial aneurysms (IA) is largely unknown. Also,...
Background The pathogenesis of development and rupture of intracranial aneurysms (IA) is largely unk...
Purpose: Through comprehensive bioinformatics analysis based on the immune microenvironment, this st...
The rupture of an intracranial aneurysm (IA) causes devastating hemorrhagic strokes. Yet, most IAs r...
Subarachnoid hemorrhage (SAH) is a major cause of death and morbidity worldwide, often due to ruptur...
BackgroundThe rupture of an intracranial aneurysm (IA) causes devastating subarachnoid hemorrhages, ...
Peripheral blood mononuclear cells (PBMCs) play an important role in the inflammation that accompani...
Background: Ruptured intracranial aneurysm (IA) is a disease with high mortality. Despite the great ...
ABSTRACT Background: Subarachnoid haemorrhage is a devastating disease with high morbidity and morta...
OBJECTIVE: To gain comprehensive insight into the molecular mechanism of formation and rupture of in...
BackgroundIt is well known that ruptured intracranial aneurysms are associated with substantial morb...
We tried to identify molecular markers in peripheral blood to predict high risk of aneurysm rupture....
Background and Purpose - Analyzing genes involved in development and rupture of intracranial aneurys...
Background: Recently, common genetic risk factors for intracranial aneurysm (IA) and aneurysmal suba...
Candidate gene studies have identified genetic variants associated with clinical outcomes following ...