Results 41 to 50 of about 230,811 (245)

Case report: Meningitis and intracranial aneurysm caused by mixed infection of oral microflora dominated by anaerobes

open access: yesFrontiers in Neurology, 2022
IntroductionMeningitis caused by oral anaerobic bacteria is rare, especially when complicated with an infected intracranial aneurysm. This paper has described an extremely rare case of bacterial meningitis caused by a mixed infection of oral microflora ...
Hongjiang Cheng   +12 more
doaj   +1 more source

Genetics of Intracranial Aneurysms

open access: yesStroke, 2021
Rupture of an intracranial aneurysm leads to aneurysmal subarachnoid hemorrhage, a severe type of stroke which is, in part, driven by genetic variation. In the past 10 years, genetic studies of IA have boosted the number of known genetic risk factors and improved our understanding of the disease.
Mark K. Bakker, Ynte M. Ruigrok
openaire   +3 more sources

Stroke‐Heart Syndrome: Mechanisms, Temporal Phenotypes, and Diagnostic Reasoning

open access: yesAdvanced Science, EarlyView.
Stroke‐heart syndrome describes new or worsened cardiac abnormalities after acute stroke. This Review defines its clinical boundaries, traces autonomic, inflammatory, endothelial, and supply‐demand mechanisms across time, and proposes provisional phenotypes that integrate lesion location, premorbid cardiac substrate, serial biomarkers ...
Fa Lin   +13 more
wiley   +1 more source

Spontaneous subarachnoid haemorrhage due to coarctation of aorta and intraspinal collaterals : a rare presentation [PDF]

open access: yes, 2012
The occurrence of spontaneous subarachnoid haemorrhage (SAH) in association with coarctation of thoracic aorta and absence of intracranial aneurysm is a rare association.
Devara, Anil K.V.   +2 more
core  

Patient information after ruptured intracranial aneurysm

open access: yes, 2004
Aim. This paper reports an investigation into the effects of increased information for patients treated for intracranial aneurysm rupture. Background. Intracranial aneurysm rupture is a grave condition that requires immediate care.
von Vogelsang, Ann-Christin   +11 more
core   +1 more source

Mouse models of intracranial aneurysm [PDF]

open access: yes, 2014
Subarachnoid hemorrhage secondary to rupture of an intracranial aneurysm is a highly lethal medical condition. Current management strategies for unruptured intracranial aneurysms involve radiological surveillance and neurosurgical or endovascular ...
Jonathan Golledge   +16 more
core   +1 more source

A case report of ruptured intracranial dissecting aneurysm associated with neurosyphilis

open access: yesInterdisciplinary Neurosurgery
Intracranial dissecting aneurysm secondary to neurosyphilis is rare with only sporadic literature. Due to the insidious nature of the disease, as well as the rapid and dynamic changes of the intectious intracranial aneurysm, the outcome of treatment was ...
Ziwei Xu   +7 more
doaj   +1 more source

A visual risk assessment tool for acute kidney injury after intracranial aneurysm clipping surgery

open access: yesRenal Failure, 2020
Objective The aim of the study was to establish a predictive postoperative nomogram for acute kidney injury (AKI) after intracranial aneurysm clipping surgery, in order to early identify patients with high postoperative AKI risk.
Pei Zhang   +13 more
doaj   +1 more source

Genetics of Intracranial Aneurysms [PDF]

open access: yesStroke, 2018
Intracranial aneurysms (IAs) are localized dilatations of intracranial arteries that are because of weaknesses of the endothelial layer. These dilations vary in size (small aneurysms, 25 mm) and are classified according to their shapes: either localized sac-like pouches or long dilatations that increase the vessels diameter; these shapes are referred ...
Sirui, Zhou   +2 more
openaire   +2 more sources

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto   +5 more
wiley   +1 more source

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