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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 3
1996 2
1997 5
1998 9
1999 9
2000 12
2001 7
2002 13
2003 6
2004 11
2005 15
2006 17
2007 18
2008 14
2009 18
2010 19
2011 17
2012 13
2013 7
2014 15
2015 11
2016 15
2017 20
2018 14
2019 18
2020 13
2021 12
2022 7
2023 6

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322 results

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Page 1
CNS small vessel disease: A clinical review.
Cannistraro RJ, Badi M, Eidelman BH, Dickson DW, Middlebrooks EH, Meschia JF. Cannistraro RJ, et al. Neurology. 2019 Jun 11;92(24):1146-1156. doi: 10.1212/WNL.0000000000007654. Epub 2019 May 29. Neurology. 2019. PMID: 31142635 Free PMC article. Review.
Known causes and risk factors include age, hypertension, branch atheromatous disease, cerebral amyloid angiopathy, radiation exposure, immune-mediated vasculitides, certain infections, and several genetic diseases. ...CSVD is diagnosed on the basis of brain imaging biomark …
Known causes and risk factors include age, hypertension, branch atheromatous disease, cerebral amyloid angiopathy, radiation exposure …
CADASIL.
Wang MM. Wang MM. Handb Clin Neurol. 2018;148:733-743. doi: 10.1016/B978-0-444-64076-5.00047-8. Handb Clin Neurol. 2018. PMID: 29478611 Review.
The most prevalent inherited cause of cerebral small-vessel disease is CADASIL, cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy, a disorder linked to mutations in NOTCH3. ... …
The most prevalent inherited cause of cerebral small-vessel disease is CADASIL, cerebral autosomal-dominant …
An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies.
Ashrafi MR, Amanat M, Garshasbi M, Kameli R, Nilipour Y, Heidari M, Rezaei Z, Tavasoli AR. Ashrafi MR, et al. Expert Rev Neurother. 2020 Jan;20(1):65-84. doi: 10.1080/14737175.2020.1699060. Epub 2019 Dec 12. Expert Rev Neurother. 2020. PMID: 31829048 Review.
New genetic methods and stem cell transplantation are also under investigation to further increase the quality and duration of life in affected population.Expert opinion: The improvements in molecular diagnostic tools allow us to identify the meticulous underlying etiology of leu …
New genetic methods and stem cell transplantation are also under investigation to further increase the quality and duration of life in affec …
Cadasil.
Chabriat H, Joutel A, Dichgans M, Tournier-Lasserve E, Bousser MG. Chabriat H, et al. Lancet Neurol. 2009 Jul;8(7):643-53. doi: 10.1016/S1474-4422(09)70127-9. Lancet Neurol. 2009. PMID: 19539236 Review.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is the most common heritable cause of stroke and vascular dementia in adults. ...A recent multicentre trial in patients with cogni …
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CAD …
Migraine and stroke.
Zhang Y, Parikh A, Qian S. Zhang Y, et al. Stroke Vasc Neurol. 2017 May 29;2(3):160-167. doi: 10.1136/svn-2017-000077. eCollection 2017 Sep. Stroke Vasc Neurol. 2017. PMID: 28989805 Free PMC article. Review.
Migraine is also shown to be correlated to haemorrhagic stroke, although studies do not demonstrate causation versus association, and further studies are warranted. There are also some rare genetic diseases such as cerebral autosomal-dominant arteriopathy …
Migraine is also shown to be correlated to haemorrhagic stroke, although studies do not demonstrate causation versus association, and furthe …
White Matter Diseases with Radiologic-Pathologic Correlation.
Sarbu N, Shih RY, Jones RV, Horkayne-Szakaly I, Oleaga L, Smirniotopoulos JG. Sarbu N, et al. Radiographics. 2016 Sep-Oct;36(5):1426-47. doi: 10.1148/rg.2016160031. Radiographics. 2016. PMID: 27618323 Updated. Review.
Autoimmune processes include multiple sclerosis and related diseases: tumefactive demyelinating lesions, Balo concentric sclerosis, Marburg and Schilder variants, neuromyelitis optica (Devic disease), acute disseminated encephalomyelitis, and acute hemorrhagic leukoencephalopa …
Autoimmune processes include multiple sclerosis and related diseases: tumefactive demyelinating lesions, Balo concentric sclerosis, Marburg …
Cerebral Microbleeds: Imaging and Clinical Significance.
Haller S, Vernooij MW, Kuijer JPA, Larsson EM, Jäger HR, Barkhof F. Haller S, et al. Radiology. 2018 Apr;287(1):11-28. doi: 10.1148/radiol.2018170803. Radiology. 2018. PMID: 29558307 Free article. Review.
Cerebral microbleeds (CMBs), also referred to as microhemorrhages, appear on magnetic resonance (MR) images as hypointense foci notably at T2*-weighted or susceptibility-weighted (SW) imaging. ...Because of the more widespread availability of high-field-strength MR imaging …
Cerebral microbleeds (CMBs), also referred to as microhemorrhages, appear on magnetic resonance (MR) images as hypointense foci notab …
Endothelial/pericyte interactions.
Armulik A, Abramsson A, Betsholtz C. Armulik A, et al. Circ Res. 2005 Sep 16;97(6):512-23. doi: 10.1161/01.RES.0000182903.16652.d7. Circ Res. 2005. PMID: 16166562 Review.
Abnormal interactions between the 2 cell types are also implicated in a number of human pathological conditions, including tumor angiogenesis, diabetic microangiopathy, ectopic tissue calcification, and stroke and dementia syndrome CADASIL. In the present review, we summar …
Abnormal interactions between the 2 cell types are also implicated in a number of human pathological conditions, including tumor angiogenesi …
Heritable and non-heritable uncommon causes of stroke.
Bersano A, Kraemer M, Burlina A, Mancuso M, Finsterer J, Sacco S, Salvarani C, Caputi L, Chabriat H, Oberstein SL, Federico A, Lasserve ET, Hunt D, Dichgans M, Arnold M, Debette S, Markus HS. Bersano A, et al. J Neurol. 2021 Aug;268(8):2780-2807. doi: 10.1007/s00415-020-09836-x. Epub 2020 Apr 21. J Neurol. 2021. PMID: 32318851 Review.
CADASIL: new advances in basic science and clinical perspectives.
Ferrante EA, Cudrici CD, Boehm M. Ferrante EA, et al. Curr Opin Hematol. 2019 May;26(3):193-198. doi: 10.1097/MOH.0000000000000497. Curr Opin Hematol. 2019. PMID: 30855338 Free PMC article. Review.
PURPOSE OF REVIEW: Recent advances in genetic evaluation improved the identification of several variants in the NOTCH3 gene causing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADA …
PURPOSE OF REVIEW: Recent advances in genetic evaluation improved the identification of several variants in the NOTCH3 gene causing Cereb …
322 results