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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
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We are analyzing https://link.springer.com/article/10.1007/bf02252926.

Title:
Brain iron and ferritin in Parkinson's and Alzheimer's diseases | Journal of Neural Transmission: Parkinson's Disease a and Dementia Section
Description:
Semiquantitative histological evaluation of brain iron and ferritin in Parkinson
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Health & Fitness

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

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

🌠 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.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Link.springer.com Make Money? {💸}

The income method remains a mystery to us.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {🔍}

article, google, scholar, pubmed, cas, iron, disease, brain, parkinsons, ferritin, alzheimers, jellinger, riederer, content, youdim, nigra, neurol, substantia, neurochem, neural, parkinsonian, brains, access, neurology, human, mbh, sci, agid, privacy, cookies, journal, grundkeiqbal, microglia, res, dexter, jenner, marsden, central, press, joshi, usa, biochem, clinical, information, publish, research, search, dementia, paulus, selective,

Topics {✒️}

month download article/chapter nincds/adrda work group soluble antigen-antibody complex horseradish peroxidase-antihorseradisch peroxidase iron-induced lipid peroxidation full article pdf melanin induced neurodegeneration mptp-mpp+-induced neurotoxicity privacy choices/manage cookies orlando san diego ludwig boltzmann institute related subjects substantia nigra resulting european economic area included frontal cortex damaged areas devoid oxidative stress van woert mh post mortem distribution long term consequences dopaminergic neurotransmission int regulatory rna sequences metal irons occurring free radical reactions calcium-binding protein 28-kilo-dalton calbindin active neuropathological process selective nigra toxicity article journal article jellinger conditions privacy policy control mrna levels magnetic resonance imaging clinico-pathological analysis total iron content article log faint iron staining iron responsive elements iron-responsive element iron storage protein glutathione peroxidase activity ben-shachar accepting optional cookies forno ls strong ferritin reactivity strong ferritin immunoreactivity journal finder publish decreased ferritin levels article cite significant selective increase

Questions {❓}

  • Gerber MR, Connor JR (1989) Do oligodendrocytes mediate iron regulation in human brain?
  • Youdim MBH, Ben-Shachar D, Riederer P (1989) Is Parkinson's disease a progressive siderosis of substantia nigra resulting in iron and melanin induced neurodegeneration?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Brain iron and ferritin in Parkinson's and Alzheimer's diseases
         description:Semiquantitative histological evaluation of brain iron and ferritin in Parkinson's (PD) and Alzheimer's disease (DAT) have been performed in paraffin sections of brain regions which included frontal cortex, hippocampus, basal ganglia and brain stem. The results indicate a significant selective increase of Fe3+ and ferritin in substantia nigra zona compacta but not in zona reticulata of Parkinsonian brains, confirming the biochemical estimation of iron. No such changes were observed in the same regions of DAT brains. The increase of iron is evident in astrocytes, macrophages, reactive microglia and non-pigmented neurons, and in damaged areas devoid of pigmented neurons. In substantia nigra of PD and PD/DAT, strong ferritin reactivity was also associated with proliferated microglia. A faint iron staining was seen occasionally in peripheral halo of Lewy bodies. By contrast, in DAT and PD/DAT, strong ferritin immunoreactivity was observed in and around senile plaques and neurofibrillary tangles. The interrelationship between selective increase of iron and ferritin in PD requires further investigation, because both changes could participate in the induction of oxidative stress and neuronal dath, due to their ability to promote formation of oxygen radicals.
         datePublished:1990-12-01T00:00:00Z
         dateModified:1990-12-01T00:00:00Z
         pageStart:327
         pageEnd:340
         sameAs:https://doi.org/10.1007/BF02252926
         keywords:
            Iron
            ferritin
            Parkinson's disease
            Alzheimer's disease
            melanin
            Lewy body
            Neurology
         image:
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            name:Journal of Neural Transmission - Parkinson's Disease and Dementia Section
            issn:
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               PublicationVolume
         publisher:
            name:Springer Vienna
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               type:ImageObject
            type:Organization
         author:
               name:K. Jellinger
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                     name:University of Würzburg School of Medicine
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ScholarlyArticle:
      headline:Brain iron and ferritin in Parkinson's and Alzheimer's diseases
      description:Semiquantitative histological evaluation of brain iron and ferritin in Parkinson's (PD) and Alzheimer's disease (DAT) have been performed in paraffin sections of brain regions which included frontal cortex, hippocampus, basal ganglia and brain stem. The results indicate a significant selective increase of Fe3+ and ferritin in substantia nigra zona compacta but not in zona reticulata of Parkinsonian brains, confirming the biochemical estimation of iron. No such changes were observed in the same regions of DAT brains. The increase of iron is evident in astrocytes, macrophages, reactive microglia and non-pigmented neurons, and in damaged areas devoid of pigmented neurons. In substantia nigra of PD and PD/DAT, strong ferritin reactivity was also associated with proliferated microglia. A faint iron staining was seen occasionally in peripheral halo of Lewy bodies. By contrast, in DAT and PD/DAT, strong ferritin immunoreactivity was observed in and around senile plaques and neurofibrillary tangles. The interrelationship between selective increase of iron and ferritin in PD requires further investigation, because both changes could participate in the induction of oxidative stress and neuronal dath, due to their ability to promote formation of oxygen radicals.
      datePublished:1990-12-01T00:00:00Z
      dateModified:1990-12-01T00:00:00Z
      pageStart:327
      pageEnd:340
      sameAs:https://doi.org/10.1007/BF02252926
      keywords:
         Iron
         ferritin
         Parkinson's disease
         Alzheimer's disease
         melanin
         Lewy body
         Neurology
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                  name:University of Würzburg School of Medicine
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               name:Ludwig Boltzmann Institute of Clinical Neurobiology, Lainz Hospital, Vienna, Austria
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               name:Ludwig Boltzmann Institute of Clinical Neurobiology, Lainz Hospital, Vienna, Austria
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            name:NYS Institute for Basic Research in Developmental Disabilities
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            name:Technion, Faculty of Medicine
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      name:Ludwig Boltzmann Institute of Clinical Neurobiology, Lainz Hospital, Vienna, Austria
      name:Ludwig Boltzmann Institute of Clinical Neurobiology, Lainz Hospital, Vienna, Austria
      name:NYS Institute for Basic Research in Developmental Disabilities, Staten Island, USA
      name:Clinical Neurochemistry, Department of Psychiatry, University of Würzburg School of Medicine, Würzburg, Federal Republic of Germany
      name:Department of Pharmacology, Technion, Faculty of Medicine, Haifa, Israel
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External Links {🔗}(162)

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