نتایج جستجو برای: leukoaraiosis

تعداد نتایج: 714  

2006
Heather Fullerton Gabrielle deVeber

Tissue Plasminogen Activator 7351C/T Polymorphism and Lacunar Stroke To the Editor: Jannes et al1 reported that a polymorphism in the tissue plasminogen activator (tPA) gene ( 7351C/T) was associated with ischemic stroke in an Australian population. Stratification for stroke subtype demonstrated an association with lacunar infarction (OR: 2.7; 95% CI, 1.1 to 6.7), but not with other stroke subt...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2002
A Hassan A Lansbury A J Catto A Guthrie J Spencer C Craven P J Grant J M Bamford

OBJECTIVES Pathological and clinical data suggest that patients presenting with ischaemic lacunar syndromes may be a heterogenous group. Those with isolated lacunar infarction are thought to have localised atherosclerosis whereas in those with coexisting leukoaraiois a distinct diffuse small vessel vasculopathy may be the predominant underlying pathology. The ACE insertion/deletion (I/D) polymo...

Journal: :Stroke 2004
Wai Kwong Tang Sandra S M Chan Helen F K Chiu Gabor S Ungvari Ka Sing Wong Timothy C Y Kwok Vincent Mok K T Wong Polly S Richards A T Ahuja

BACKGROUND AND PURPOSE Both dementia and stroke are major health problems in Chinese societies. Stroke is a frequent cause of dementia. Only a few studies have been published on poststroke dementia (PSDE), none of which has investigated a consecutive stroke cohort in Asian patient populations. The objective of this study was to examine the prevalence and clinical correlates of PSDE in Chinese s...

Journal: :Hypertension 1999
K Kohara Y Jiang M Igase Y Takata T Fukuoka T Okura Y Kitami K Hiwada

offelucidate the relationship between postprandial hypotension (PPH) and asymptomatic cerebrovascular damage, we evaluated changes in blood pressure after a meal by 24-hour blood pressure monitoring in 70 hospitalized essential hypertensive patients aged >/=50 years. They received a diet containing standard nutritional ingredients with 120 mmol (7 g) NaCl and were free from medication for at le...

2015
Laura L. Kilarski Loes C. A. Rutten-Jacobs Steve Bevan Rob Baker Ahamad Hassan Derralynn A. Hughes Hugh S. Markus Namik Kaya

BACKGROUND AND PURPOSE Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), caused by mutations in the NOTCH3 gene, is the most common monogenic disorder causing lacunar stroke and cerebral small vessel disease (SVD). Fabry disease (FD) due to mutations in the GLA gene has been suggested as an underdiagnosed cause of stroke, and one feature is SV...

Journal: :Alzheimers & Dementia 2023

Background Intracranial arteriosclerosis has been increasingly recognized as an etiological factor contributing to cognitive impairment. Indigenous Tsimane and Moseten, Amerindians of the Bolivian Amazon with physically-active subsistence lifestyle, are reported have lower prevalence dementia (Gatz et al., Alzheimer’s Dement, In press) coronary artery disease (Kaplan al.,Lancet,2017) than Weste...

Journal: :Annals of Clinical and Translational Neurology 2020

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