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  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Doi.org Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
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We began analyzing https://link.springer.com/article/10.1007/s00415-016-8220-2, but it redirected us to https://link.springer.com/article/10.1007/s00415-016-8220-2. The analysis below is for the second page.

Title[redir]:
Cerebral microbleeds in early Alzheimer’s disease | Journal of Neurology
Description:
We hypothesize that cerebral microbleeds (CMB) in patients with different neuropsychological profiles (amnestic or non-amnestic) and MRI features of vascular damage could provide important information on the underlying pathological process in early Alzheimer’s disease. The study was performed at two trial sites. We studied 136 outpatients with cognitive decline. MRI was performed using a magnetic field of 1.5 and 3 T. Neuropsychological assessment included Mini-Mental State Examination (MMSE), Montreal Cognitive Assessment scale (MoCA), Addenbrooke’s Cognitive Examination (ACE-R), Cambridge Cognitive Examination battery (CAMCOG) (Part 3), Clock Drawing Test, fluency test and the visual memory test (SCT). CSF was examined for standard parameters such as tau, phosphorylated tau, amyloid-β 1–40 and 42 and Qalbumin, in accordance with established protocols and genotype. In 61 patients (45 %), at least 1 CMB was found. Most of the CMBs were described in the amnestic profile (67 %). In 86 % of the cases, multiple CMB were observed. The ratio of Aβ1-40/42 in non-amnestic patients with CMB was significantly lower (mean 0.6) than in patients without CMB (mean 1.2). A notable difference in the albumin ratio as an indicator of the BBB was observed between groups with and without CMB. In the CMP-positive group, the E2 genotype was observed more frequently, and the E4 genotype less frequently, than in the CMB-negative group. Based on the cerebrospinal fluid–serum albumin ratio, we were able to show that patients with CMB present several features of BBB dysfunction. According to logistic regression, the predictive factors for CMB in patients with cognitive decline were age, WMHs score and albumin ratio. We found a significant reduction in the Aβ-amyloid ratio in the non-amnestic profile group with CMB (particularly in the cortical region) in comparison to those without CMB. While this is an interesting finding, its significance needs to be assessed in a prospective follow-up.

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Social Networks

Content Management System {📝}

What CMS is doi.org built with?

Custom-built

No common CMS systems were detected on Doi.org, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of doi.org audience?

🏙️ Massive Traffic: 50M - 100M visitors per month


Based on our best estimate, this website will receive around 80,904,851 visitors per month in the current month.

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How Does Doi.org Make Money? {💸}

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. Doi.org might be plotting its profit, but the way they're doing it isn't detectable yet.

Keywords {🔍}

pubmed, article, google, scholar, cognitive, microbleeds, disease, alzheimers, impairment, patients, cerebral, cas, mild, central, dementia, neurol, cmb, van, csf, ratio, clinical, stroke, research, neurology, cerebrospinal, biomarkers, dis, barrier, privacy, cookies, content, journal, zerr, vascular, tau, dysfunction, access, brain, liu, bloodbrain, alzheimer, function, information, publish, search, early, poliakova, mri, study, decline,

Topics {✒️}

age-related white matter blood-brain barrier dysfunction magnetic resonance imaging month download article/chapter /books/understanding-alzheimer-s-disease magnetic resonance neuroimaging increased protein-conjugated acrolein susceptibility-weighted imaging van der flier georg-august-universität göttingen vascular damage map brain microbleeds silent brain infarctions full article pdf van der lugt mild cognitive impairment privacy choices/manage cookies cognitive examination revised van gool wa cerebrospinal fluid levels subjective cognitive impairment cerebrospinal fluid biomarkers cerebrospinal fluid profiles van berckel bn small vessel disease multiple cerebral microbleeds brain microbleeds aβ-amyloid ratio amyloid -β40/42 ratio cognitive test battery schuit rc russian–german grant ethics declarations conflicts related subjects check access al-shahi salman instant access vascular cognitive impairment high amyloid-β european economic area scope submit manuscript underlying pathological process magnetic field cmp-positive group monge-argilés ja advanced periventricular leukoaraiosis cerebrospinal fluid apolipoprotein wahlund lo �stage-dependent biochemical national reference center

Questions {❓}

  • Lim YY, Ellis KA, Harrington K, Pietrzak RH, Gale J, Ames D, Bush AI, Darby D, Martins RN, Masters CL, Rowe C, Savage G, Szoeke C, Villemagne VL, Maruff P (2013) Cognitive decline in adults with amnestic mild cognitive impairment and high amyloid-β: prodromal Alzheimer’s disease?
  • Mitchell AJ, Monge-ArgilĂŠs JA, SĂĄnchez-Paya J (2010) Do CSF biomarkers help clinicians predict the progression of mild cognitive impairment to dementia?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Cerebral microbleeds in early Alzheimer’s disease
         description:We hypothesize that cerebral microbleeds (CMB) in patients with different neuropsychological profiles (amnestic or non-amnestic) and MRI features of vascular damage could provide important information on the underlying pathological process in early Alzheimer’s disease. The study was performed at two trial sites. We studied 136 outpatients with cognitive decline. MRI was performed using a magnetic field of 1.5 and 3 T. Neuropsychological assessment included Mini-Mental State Examination (MMSE), Montreal Cognitive Assessment scale (MoCA), Addenbrooke’s Cognitive Examination (ACE-R), Cambridge Cognitive Examination battery (CAMCOG) (Part 3), Clock Drawing Test, fluency test and the visual memory test (SCT). CSF was examined for standard parameters such as tau, phosphorylated tau, amyloid-β 1–40 and 42 and Qalbumin, in accordance with established protocols and genotype. In 61 patients (45 %), at least 1 CMB was found. Most of the CMBs were described in the amnestic profile (67 %). In 86 % of the cases, multiple CMB were observed. The ratio of Aβ1-40/42 in non-amnestic patients with CMB was significantly lower (mean 0.6) than in patients without CMB (mean 1.2). A notable difference in the albumin ratio as an indicator of the BBB was observed between groups with and without CMB. In the CMP-positive group, the E2 genotype was observed more frequently, and the E4 genotype less frequently, than in the CMB-negative group. Based on the cerebrospinal fluid–serum albumin ratio, we were able to show that patients with CMB present several features of BBB dysfunction. According to logistic regression, the predictive factors for CMB in patients with cognitive decline were age, WMHs score and albumin ratio. We found a significant reduction in the Aβ-amyloid ratio in the non-amnestic profile group with CMB (particularly in the cortical region) in comparison to those without CMB. While this is an interesting finding, its significance needs to be assessed in a prospective follow-up.
         datePublished:2016-07-07T00:00:00Z
         dateModified:2016-07-07T00:00:00Z
         pageStart:1961
         pageEnd:1968
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            Mild cognitive impairment
            Alzheimer disease
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      headline:Cerebral microbleeds in early Alzheimer’s disease
      description:We hypothesize that cerebral microbleeds (CMB) in patients with different neuropsychological profiles (amnestic or non-amnestic) and MRI features of vascular damage could provide important information on the underlying pathological process in early Alzheimer’s disease. The study was performed at two trial sites. We studied 136 outpatients with cognitive decline. MRI was performed using a magnetic field of 1.5 and 3 T. Neuropsychological assessment included Mini-Mental State Examination (MMSE), Montreal Cognitive Assessment scale (MoCA), Addenbrooke’s Cognitive Examination (ACE-R), Cambridge Cognitive Examination battery (CAMCOG) (Part 3), Clock Drawing Test, fluency test and the visual memory test (SCT). CSF was examined for standard parameters such as tau, phosphorylated tau, amyloid-β 1–40 and 42 and Qalbumin, in accordance with established protocols and genotype. In 61 patients (45 %), at least 1 CMB was found. Most of the CMBs were described in the amnestic profile (67 %). In 86 % of the cases, multiple CMB were observed. The ratio of Aβ1-40/42 in non-amnestic patients with CMB was significantly lower (mean 0.6) than in patients without CMB (mean 1.2). A notable difference in the albumin ratio as an indicator of the BBB was observed between groups with and without CMB. In the CMP-positive group, the E2 genotype was observed more frequently, and the E4 genotype less frequently, than in the CMB-negative group. Based on the cerebrospinal fluid–serum albumin ratio, we were able to show that patients with CMB present several features of BBB dysfunction. According to logistic regression, the predictive factors for CMB in patients with cognitive decline were age, WMHs score and albumin ratio. We found a significant reduction in the Aβ-amyloid ratio in the non-amnestic profile group with CMB (particularly in the cortical region) in comparison to those without CMB. While this is an interesting finding, its significance needs to be assessed in a prospective follow-up.
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         Cerebral microbleeds
         Mild cognitive impairment
         Alzheimer disease
         White matter lesions
         Magnetic resonance imaging
         Blood–brain barrier damage
         Neurology
         Neurosciences
         Neuroradiology
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                  address:
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      affiliation:
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            name:Clinical Hospital of S.P. Botkin
            address:
               name:Clinical Hospital of S.P. Botkin, Moscow, Russia
               type:PostalAddress
            type:Organization
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            name:Russian Medical Academy of Postgraduate Education
            address:
               name:Russian Medical Academy of Postgraduate Education, Moscow, Russia
               type:PostalAddress
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      name:I. Zerr
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            name:University Medical School, Georg-August-Universität GĂśttingen
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External Links {🔗}(186)

Analytics and Tracking {📊}

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Libraries {📚}

  • Clipboard.js
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Emails and Hosting {✉️}

Mail Servers:

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Name Servers:

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CDN Services {📦}

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