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  2. Matching Content Categories
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  5. How Does Link.springer.com Make Money
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  7. Topics
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We are analyzing https://link.springer.com/article/10.1007/s00401-011-0851-x.

Title:
Heterogeneity in age-related white matter changes | Acta Neuropathologica
Description:
White matter changes occur endemically in routine magnetic resonance imaging (MRI) scans of elderly persons. MRI appearance and histopathological correlates of white matter changes are heterogeneous. Smooth periventricular hyperintensities, including caps around the ventricular horns, periventricular lining and halos are likely to be of non-vascular origin. They relate to a disruption of the ependymal lining with subependymal widening of the extracellular space and have to be differentiated from subcortical and deep white matter abnormalities. For the latter a distinction needs to be made between punctate, early confluent and confluent types. Although punctate white matter lesions often represent widened perivascular spaces without substantial ischemic tissue damage, early confluent and confluent lesions correspond to incomplete ischemic destruction. Punctate abnormalities on MRI show a low tendency for progression, while early confluent and confluent changes progress rapidly. The causative and modifying pathways involved in the occurrence of sporadic age-related white matter changes are still incompletely understood, but recent microarray and genome-wide association approaches increased the notion of pathways that might be considered as targets for therapeutic intervention. The majority of differentially regulated transcripts in white matter lesions encode genes associated with immune function, cell cycle, proteolysis, and ion transport. Genome-wide association studies identified six SNPs mapping to a locus on chromosome 17q25 to be related to white matter lesion load in the general population. We also report first and preliminary data that demonstrate apolipoprotein E (ApoE) immunoreactivity in white matter lesions and support epidemiological findings indicating that ApoE is another factor possibly related to white matter lesion occurrence. Further insights come from modern MRI techniques, such as diffusion tensor and magnetization transfer imaging, as they provide tools for the characterization of normal-appearing brain tissue beyond what can be expected from standard MRI scans. There is a need for additional pre- and postmortem studies in humans, including these new imaging techniques.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {๐Ÿ“š}

  • Education
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Content Management System {๐Ÿ“}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {๐Ÿ“ˆ}

What is the average monthly size of link.springer.com audience?

๐ŸŒ  Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {๐Ÿ’ธ}

We don't see any clear sign of profit-making.

Many websites are intended to earn money, but some serve to share ideas or build connections. Websites exist for all kinds of purposes. This might be one of them. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {๐Ÿ”}

google, scholar, matter, white, pubmed, article, cas, imaging, mri, lesions, study, hyperintensities, stroke, neurol, brain, elderly, disease, neurology, schmidt, diffusion, magnetic, resonance, cerebral, van, fazekas, tensor, postmortem, leukoaraiosis, magnetization, transfer, aging, agerelated, correlates, subcortical, ladis, psychiatry, ajnr, neuroradiol, graz, ropele, related, findings, correlation, vascular, normal, pathology, university, research, volume, pantoni,

Topics {โœ’๏ธ}

hypoxiaโ€“ischemia-induced thrombotic stroke month download article/chapter genome-wide association studies cerebral autosomal-dominant arteriopathy age-related white matter white matter integrity chronic hypoperfusion injury cerebrovascular risk profiles formalin-fixed human brain normal-appearing brain tissue community-dwelling older people late-life depressive symptoms post-mortem quantitative mri voxel-based morphometric study neuropsychological deficits post-stroke balance disorders cerebral white matter white matter hyperintensities full article pdf white matter lesions white matter microstructural periventricular white matter nonlesional white matter magnetic resonance imaging basic neuroscience research privacy choices/manage cookies brain white matter serial mr imaging small vessel disease subcortical lesions identified mr signal abnormalities post-mortem brains subcortical vascular disease incomplete ischemic destruction multiple functional pathways related subjects diffusion tensor imaging gouw aa fernando ms van den hout magnetization transfer imaging smooth periventricular hyperintensities dilated perivascular spaces van buchem ma austrian national bank factor possibly related magnetization transfer ratio postmortem mr imaging van straaten ec large epidemiological sample

Questions {โ“}

  • Spilt A, Geeraedts T, de Craen AJ, Westendorp RG, Blauw GJ, van Buchem MA (2005) Age-related changes in normal-appearing brain tissue and white matter hyperintensities: more of the same or something else?

Schema {๐Ÿ—บ๏ธ}

WebPage:
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         headline:Heterogeneity in age-related white matter changes
         description:White matter changes occur endemically in routine magnetic resonance imaging (MRI) scans of elderly persons. MRI appearance and histopathological correlates of white matter changes are heterogeneous. Smooth periventricular hyperintensities, including caps around the ventricular horns, periventricular lining and halos are likely to be of non-vascular origin. They relate to a disruption of the ependymal lining with subependymal widening of the extracellular space and have to be differentiated from subcortical and deep white matter abnormalities. For the latter a distinction needs to be made between punctate, early confluent and confluent types. Although punctate white matter lesions often represent widened perivascular spaces without substantial ischemic tissue damage, early confluent and confluent lesions correspond to incomplete ischemic destruction. Punctate abnormalities on MRI show a low tendency for progression, while early confluent and confluent changes progress rapidly. The causative and modifying pathways involved in the occurrence of sporadic age-related white matter changes are still incompletely understood, but recent microarray and genome-wide association approaches increased the notion of pathways that might be considered as targets for therapeutic intervention. The majority of differentially regulated transcripts in white matter lesions encode genes associated with immune function, cell cycle, proteolysis, and ion transport. Genome-wide association studies identified six SNPs mapping to a locus on chromosome 17q25 to be related to white matter lesion load in the general population. We also report first and preliminary data that demonstrate apolipoprotein E (ApoE) immunoreactivity in white matter lesions and support epidemiological findings indicating that ApoE is another factor possibly related to white matter lesion occurrence. Further insights come from modern MRI techniques, such as diffusion tensor and magnetization transfer imaging, as they provide tools for the characterization of normal-appearing brain tissue beyond what can be expected from standard MRI scans. There is a need for additional pre- and postmortem studies in humans, including these new imaging techniques.
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      headline:Heterogeneity in age-related white matter changes
      description:White matter changes occur endemically in routine magnetic resonance imaging (MRI) scans of elderly persons. MRI appearance and histopathological correlates of white matter changes are heterogeneous. Smooth periventricular hyperintensities, including caps around the ventricular horns, periventricular lining and halos are likely to be of non-vascular origin. They relate to a disruption of the ependymal lining with subependymal widening of the extracellular space and have to be differentiated from subcortical and deep white matter abnormalities. For the latter a distinction needs to be made between punctate, early confluent and confluent types. Although punctate white matter lesions often represent widened perivascular spaces without substantial ischemic tissue damage, early confluent and confluent lesions correspond to incomplete ischemic destruction. Punctate abnormalities on MRI show a low tendency for progression, while early confluent and confluent changes progress rapidly. The causative and modifying pathways involved in the occurrence of sporadic age-related white matter changes are still incompletely understood, but recent microarray and genome-wide association approaches increased the notion of pathways that might be considered as targets for therapeutic intervention. The majority of differentially regulated transcripts in white matter lesions encode genes associated with immune function, cell cycle, proteolysis, and ion transport. Genome-wide association studies identified six SNPs mapping to a locus on chromosome 17q25 to be related to white matter lesion load in the general population. We also report first and preliminary data that demonstrate apolipoprotein E (ApoE) immunoreactivity in white matter lesions and support epidemiological findings indicating that ApoE is another factor possibly related to white matter lesion occurrence. Further insights come from modern MRI techniques, such as diffusion tensor and magnetization transfer imaging, as they provide tools for the characterization of normal-appearing brain tissue beyond what can be expected from standard MRI scans. There is a need for additional pre- and postmortem studies in humans, including these new imaging techniques.
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               type:PostalAddress
            type:Organization
      name:Franz Fazekas
      affiliation:
            name:Medical University of Graz
            address:
               name:Division of General Neurology, Department of Neurology, Medical University of Graz, Graz, Austria
               type:PostalAddress
            type:Organization
      name:Kurt Jellinger
      affiliation:
            name:Institute of Clinical Neurobiology
            address:
               name:Institute of Clinical Neurobiology, Vienna, Austria
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Division of Special Neurology, Department of Neurology, Medical University of Graz, Graz, Austria
      name:Institute of Molecular Biology and Biochemistry, Medical University of Graz, Graz, Austria
      name:Institute of Pathology, Medical University of Graz, Graz, Austria
      name:Division of Special Neurology, Department of Neurology, Medical University of Graz, Graz, Austria
      name:Laboratory of Neuropathology, Department of Pathology and Neuropathology, State Neuropsychiatric Hospital Wagner-Jauregg, Linz, Austria
      name:Division of Special Neurology, Department of Neurology, Medical University of Graz, Graz, Austria
      name:Division of Special Neurology, Department of Neurology, Medical University of Graz, Graz, Austria
      name:Division of General Neurology, Department of Neurology, Medical University of Graz, Graz, Austria
      name:Division of General Neurology, Department of Neurology, Medical University of Graz, Graz, Austria
      name:Memory Research Unit, Department of Neurology, Helsinki University Central Hospital, Helsinki, Finland
      name:Department of Neurological and Psychiatric Sciences, University of Florence, Florence, Italy
      name:Alzheimer Centre, Department of Neurology, VU University Medical Centre, Amsterdam, The Netherlands
      name:Division of General Neurology, Department of Neurology, Medical University of Graz, Graz, Austria
      name:Institute of Clinical Neurobiology, Vienna, Austria
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