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Year Number of Results
1997 1
1999 1
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2002 2
2005 1
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2007 1
2009 1
2010 1
2011 1
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2023 1
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19 results

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Page 1
Arteriolar neuropathology in cerebral microvascular disease.
Fang C, Magaki SD, Kim RC, Kalaria RN, Vinters HV, Fisher M. Fang C, et al. Neuropathol Appl Neurobiol. 2023 Feb;49(1):e12875. doi: 10.1111/nan.12875. Neuropathol Appl Neurobiol. 2023. PMID: 36564356 Free PMC article. Review.
MVD is heterogeneous in aetiology, ranging from universal ageing to the sporadic (hypertension, sporadic cerebral amyloid angiopathy [CAA] and chronic kidney disease) and the genetic (e.g., familial CAA, cerebral autosomal dominant arteriopathy
MVD is heterogeneous in aetiology, ranging from universal ageing to the sporadic (hypertension, sporadic cerebral amyloid angiopathy …
Lacunar infarct.
Lastilla M. Lastilla M. Clin Exp Hypertens. 2006 Apr-May;28(3-4):205-15. doi: 10.1080/10641960600549082. Clin Exp Hypertens. 2006. PMID: 16833026 Review.
The term lacuna, or cerebral infarct, refers to a well-defined, subcortical ischemic lesion at the level of a single perforating artery, determined by primary disease of the latter. ...In turn, this is the result of various arterial disorders, the most freque …
The term lacuna, or cerebral infarct, refers to a well-defined, subcortical ischemic lesion at the level of a single pe …
Molecular genetics of migraine.
de Vries B, Frants RR, Ferrari MD, van den Maagdenberg AM. de Vries B, et al. Hum Genet. 2009 Jul;126(1):115-32. doi: 10.1007/s00439-009-0684-z. Epub 2009 May 20. Hum Genet. 2009. PMID: 19455354 Review.
Three FHM genes have been identified, which all encode ion transporters, suggesting that disturbances in ion and neurotransmitter balances in the brain are responsible for this migraine type, and possibly the common forms of migraine. ...Additional molecular insight …
Three FHM genes have been identified, which all encode ion transporters, suggesting that disturbances in ion and neurotransmitter balances i …
Subcortical ischaemic vascular dementia.
Román GC, Erkinjuntti T, Wallin A, Pantoni L, Chui HC. Román GC, et al. Lancet Neurol. 2002 Nov;1(7):426-36. doi: 10.1016/s1474-4422(02)00190-4. Lancet Neurol. 2002. PMID: 12849365 Review.
Vascular dementia is the second most common type of dementia. The subcortical ischaemic form (SIVD) frequently causes cognitive impairment and dementia in elderly people. ...Cerebral autosomal dominant arteriopathy with subcortical
Vascular dementia is the second most common type of dementia. The subcortical ischaemic form (SIVD) frequently causes cognitiv …
Inherited neurovascular diseases affecting cerebral blood vessels and smooth muscle.
Sam C, Li FF, Liu SL. Sam C, et al. Metab Brain Dis. 2015 Oct;30(5):1105-16. doi: 10.1007/s11011-015-9668-y. Epub 2015 Apr 21. Metab Brain Dis. 2015. PMID: 25893882 Review.
Neurovascular diseases are among the leading causes of mortality and permanent disability due to stroke, aneurysm, and other cardiovascular complications. Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoence
Neurovascular diseases are among the leading causes of mortality and permanent disability due to stroke, aneurysm, and other cardiovascular …
Stroke, cerebrovascular diseases and vascular cognitive impairment in Africa.
Akinyemi RO, Owolabi MO, Ihara M, Damasceno A, Ogunniyi A, Dotchin C, Paddick SM, Ogeng'o J, Walker R, Kalaria RN. Akinyemi RO, et al. Brain Res Bull. 2019 Feb;145:97-108. doi: 10.1016/j.brainresbull.2018.05.018. Epub 2018 May 25. Brain Res Bull. 2019. PMID: 29807146 Free PMC article. Review.
Somewhat different from high-income countries, strokes attributed to cerebral small vessel disease (SVD) are higher >30% among sub-Saharan Africans. ...Except for isolated cases of cerebral autosomal dominant arteriopathy with subcortical
Somewhat different from high-income countries, strokes attributed to cerebral small vessel disease (SVD) are higher >30% among sub …
Hereditary cerebral small vessel diseases: a review.
Federico A, Di Donato I, Bianchi S, Di Palma C, Taglia I, Dotti MT. Federico A, et al. J Neurol Sci. 2012 Nov 15;322(1-2):25-30. doi: 10.1016/j.jns.2012.07.041. Epub 2012 Aug 4. J Neurol Sci. 2012. PMID: 22868088 Review.
Clinical features and diagnostic clues of these conditions, [cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), cerebral autosomal recessive arteriopathy with …
Clinical features and diagnostic clues of these conditions, [cerebral autosomal dominant arteriopathy with su
Review: molecular genetics and pathology of hereditary small vessel diseases of the brain.
Yamamoto Y, Craggs L, Baumann M, Kalimo H, Kalaria RN. Yamamoto Y, et al. Neuropathol Appl Neurobiol. 2011 Feb;37(1):94-113. doi: 10.1111/j.1365-2990.2010.01147.x. Neuropathol Appl Neurobiol. 2011. PMID: 21062344 Review.
Advances in molecular genetics have enabled identification of several monogenic conditions involving small vessels predisposing to ischaemic and haemorrhagic strokes and diffuse white matter disease. With emphasis on cerebral autosomal dominant arteriopath
Advances in molecular genetics have enabled identification of several monogenic conditions involving small vessels predisposing to ischaemic …
l-arginine and l-NMMA for assessing cerebral endothelial dysfunction in ischaemic cerebrovascular disease: A systematic review.
Karlsson WK, Sørensen CG, Kruuse C. Karlsson WK, et al. Clin Exp Pharmacol Physiol. 2017 Jan;44(1):13-20. doi: 10.1111/1440-1681.12679. Clin Exp Pharmacol Physiol. 2017. PMID: 27704594 Review.
However, there is no consensus on methods to best estimate cerebral ED. In this systematic review, we evaluate the use of l-arginine and N(G) -monomethyl-l-arginine (l-NMMA) for assessment of cerebral ED. ...Seven studies (315 subjects) were eligible according to in …
However, there is no consensus on methods to best estimate cerebral ED. In this systematic review, we evaluate the use of l-arginine …
Diagnostic criteria for CADASIL in the International Classification of Headache Disorders (ICHD-II): are they appropriate?
Sacco S, Degan D, Carolei A. Sacco S, et al. J Headache Pain. 2010 Jun;11(3):181-6. doi: 10.1007/s10194-010-0203-6. Epub 2010 Mar 12. J Headache Pain. 2010. PMID: 20224942 Free PMC article. Review.
We reviewed the characteristics of headache in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), to verify the appropriateness of the International Classification of …
We reviewed the characteristics of headache in patients with cerebral autosomal dominant arteriopathy with su
19 results