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Quoted phrase not found in phrase index: "Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2"
Page 1
Genetic testing and counseling in the diagnosis and management of young-onset dementias.
Goldman JS. Goldman JS. Psychiatr Clin North Am. 2015 Jun;38(2):295-308. doi: 10.1016/j.psc.2015.01.008. Epub 2015 Mar 18. Psychiatr Clin North Am. 2015. PMID: 25998117 Review.
The most common hereditary dementias include Alzheimer disease, frontotemporal degeneration, Huntington disease, prion diseases, and cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy. ...Gen …
The most common hereditary dementias include Alzheimer disease, frontotemporal degeneration, Huntington disease, prion diseases, and cere …
Genetics of ischaemic stroke.
Dichgans M. Dichgans M. Lancet Neurol. 2007 Feb;6(2):149-61. doi: 10.1016/S1474-4422(07)70028-5. Lancet Neurol. 2007. PMID: 17239802 Review.
Large progress has been made in single-gene disorders associated with ischaemic stroke. The identification of NOTCH3 mutations in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy …
Large progress has been made in single-gene disorders associated with ischaemic stroke. The identification of NOTCH3 mutations in patients w …
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 …
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.
Seven studies (315 subjects) were eligible according to inclusion and exclusion criteria. Studies investigated the effect of age (n=2), type 2 diabetes mellitus (DM) (n=1), cerebral autosomal dominant arteriopathy with subcortical infa …
Seven studies (315 subjects) were eligible according to inclusion and exclusion criteria. Studies investigated the effect of age (n=2), t …
Do Attachment Style and Emotion Regulation Strategies Indicate Distress in Predictive Testing?
van der Meer LB, van Duijn E, Giltay EJ, Tibben A. van der Meer LB, et al. J Genet Couns. 2015 Oct;24(5):862-71. doi: 10.1007/s10897-015-9822-z. Epub 2015 Feb 3. J Genet Couns. 2015. PMID: 25641254 Free PMC article.
Predictive genetic testing for a neurogenetic disorder evokes strong emotions, and may lead to distress. ...Self-report scales were used to assess attachment insecurity (anxiety and avoidance) and maladaptive emotion regulation strategies (self-blame, rumination, catastrop …
Predictive genetic testing for a neurogenetic disorder evokes strong emotions, and may lead to distress. ...Self-report scales were u …
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain.
Monet-Leprêtre M, Bardot B, Lemaire B, Domenga V, Godin O, Dichgans M, Tournier-Lasserve E, Cohen-Tannoudji M, Chabriat H, Joutel A. Monet-Leprêtre M, et al. Brain. 2009 Jun;132(Pt 6):1601-12. doi: 10.1093/brain/awp049. Epub 2009 Mar 17. Brain. 2009. PMID: 19293235 Free PMC article.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an autosomal dominant small-vessel disease of the brain caused by mutations in the NOTCH3 receptor. ...By …
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy …