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For: De Guio F, Duering M, Fazekas F, De Leeuw FE, Greenberg SM, Pantoni L, Aghetti A, Smith EE, Wardlaw J, Jouvent E. Brain atrophy in cerebral small vessel diseases: Extent, consequences, technical limitations and perspectives: The HARNESS initiative. J Cereb Blood Flow Metab 2020;40:231-45. [PMID: 31744377 DOI: 10.1177/0271678X19888967] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Ellström K, Abul-Kasim K, Siennicki-Lantz A, Elmståhl S. Associations of carotid artery flow parameters with MRI markers of cerebral small vessel disease and patterns of brain atrophy. J Stroke Cerebrovasc Dis 2023;32:106981. [PMID: 36657270 DOI: 10.1016/j.jstrokecerebrovasdis.2023.106981] [Reference Citation Analysis]
2 Pál É, Ungvári Z, Benyó Z, Várbíró S. Role of Vitamin D Deficiency in the Pathogenesis of Cardiovascular and Cerebrovascular Diseases. Nutrients 2023;15. [PMID: 36678205 DOI: 10.3390/nu15020334] [Reference Citation Analysis]
3 Kapasi A, Schneider JA, Yu L, Lamar M, Bennett DA, Boyle PA. Association of Stroke and Cerebrovascular Pathologies With Scam Susceptibility in Older Adults. JAMA Neurol 2023;80:49-57. [PMID: 36315115 DOI: 10.1001/jamaneurol.2022.3711] [Reference Citation Analysis]
4 Dupé C, Guey S, Biard L, Dieng S, Lebenberg J, Grosset L, Alili N, Hervé D, Tournier-Lasserve E, Jouvent E, Chevret S, Chabriat H. Phenotypic variability in 446 CADASIL patients: Impact of NOTCH3 gene mutation location in addition to the effects of age, sex and vascular risk factors. J Cereb Blood Flow Metab 2023;43:153-66. [PMID: 36254369 DOI: 10.1177/0271678X221126280] [Reference Citation Analysis]
5 Moskovko SP, Bartiuk RS. Brain morphometry and its relevance in cerebral small vessel disease. Rep of Morph 2022;28:11-17. [DOI: 10.31393/morphology-journal-2022-28(4)-02] [Reference Citation Analysis]
6 Wang S, Zhang F, Huang P, Hong H, Jiaerken Y, Yu X, Zhang R, Zeng Q, Zhang Y, Kikinis R, Rathi Y, Makris N, Lou M, Pasternak O, Zhang M, O'Donnell LJ. Superficial white matter microstructure affects processing speed in cerebral small vessel disease. Hum Brain Mapp 2022;43:5310-25. [PMID: 35822593 DOI: 10.1002/hbm.26004] [Reference Citation Analysis]
7 Quick S, Procter TV, Moss J, Seeker L, Walton M, Lawson A, Baker S, Beletski A, Garcia DJ, Mohammad M, Mungall W, Onishi A, Tobola Z, Stringer M, Jansen MA, Vallatos A, Giarratano Y, Bernabeu MO, Wardlaw JM, Williams A. Loss of the heterogeneous expression of flippase ATP11B leads to cerebral small vessel disease in a normotensive rat model. Acta Neuropathol 2022. [PMID: 35635573 DOI: 10.1007/s00401-022-02441-4] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 Lebenberg J, Guichard JP, Guillonnet A, Hervé D, Alili N, Taleb A, Dias-Gastellier N, Chabriat H, Jouvent E. The Epidermal Growth Factor Domain of the Mutation Does Not Appear to Influence Disease Progression in CADASIL When Brain Volume and Sex Are Taken into Account. AJNR Am J Neuroradiol 2022;43:715-20. [PMID: 35487587 DOI: 10.3174/ajnr.A7499] [Reference Citation Analysis]
9 Tan CH, Chew J, Zhang L, Gulyás B, Chen C. Differential Effects of White Matter Hyperintensities and Regional Amyloid Deposition on Regional Cortical Thickness. Neurobiology of Aging 2022. [DOI: 10.1016/j.neurobiolaging.2022.03.013] [Reference Citation Analysis]
10 Fouto AR, Nunes RG, Pinto J, Alves L, Calado S, Gonçalves C, Rebolo M, Viana-baptista M, Vilela P, Figueiredo P. Impact of white-matter mask selection on DTI histogram-based metrics as potential biomarkers in cerebral small vessel disease. Magn Reson Mater Phy 2022;35:779-790. [DOI: 10.1007/s10334-021-00991-4] [Reference Citation Analysis]
11 Quick S, Procter TV, Moss J, Lawson A, Baker S, Walton M, Mohammad M, Mungall W, Onishi A, Tobola Z, Stringer M, Jansen MA, Vallatos A, Giarratano Y, Bernabeu MO, Wardlaw JM, Williams AC. An intrinsic endothelial dysfunction causes cerebral small vessel disease.. [DOI: 10.1101/2021.12.13.472377] [Reference Citation Analysis]
12 Fiford CM, Sudre CH, Young AL, Macdougall A, Nicholas J, Manning EN, Malone IB, Walsh P, Goodkin O, Pemberton HG, Barkhof F, Alexander DC, Cardoso MJ, Biessels GJ, Barnes J; Alzheimer’s Disease Neuroimaging Initiative. Presumed small vessel disease, imaging and cognition markers in the Alzheimer's Disease Neuroimaging Initiative. Brain Commun 2021;3:fcab226. [PMID: 34661106 DOI: 10.1093/braincomms/fcab226] [Reference Citation Analysis]
13 Subotic A, McCreary CR, Saad F, Nguyen A, Alvarez-Veronesi A, Zwiers AM, Charlton A, Beaudin AE, Ismail Z, Pike GB, Smith EE. Cortical Thickness and Its Association with Clinical Cognitive and Neuroimaging Markers in Cerebral Amyloid Angiopathy. J Alzheimers Dis 2021;81:1663-71. [PMID: 33998545 DOI: 10.3233/JAD-210138] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
14 Cui L, Chen K, Huang L, Sun J, Lv Y, Jia X, Guo Q. Changes in local brain function in mild cognitive impairment due to semantic dementia. CNS Neurosci Ther 2021;27:587-602. [PMID: 33650764 DOI: 10.1111/cns.13621] [Reference Citation Analysis]
15 Fruhwirth V, Enzinger C, Fandler-Höfler S, Kneihsl M, Eppinger S, Ropele S, Schmidt R, Gattringer T, Pinter D. Baseline white matter hyperintensities affect the course of cognitive function after small vessel disease-related stroke: a prospective observational study. Eur J Neurol 2021;28:401-10. [PMID: 33065757 DOI: 10.1111/ene.14593] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
16 Heinen R, Groeneveld ON, Barkhof F, de Bresser J, Exalto LG, Kuijf HJ, Prins ND, Scheltens P, van der Flier WM, Biessels GJ; TRACE‐VCI study group. Small vessel disease lesion type and brain atrophy: The role of co-occurring amyloid. Alzheimers Dement (Amst) 2020;12:e12060. [PMID: 32695872 DOI: 10.1002/dad2.12060] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]