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About:
Neuropathologic features of four autopsied COVID‐19 patients
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
wasabi.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Neuropathologic features of four autopsied COVID‐19 patients
Creator
Vapalahti, Olli
Kantele, Anu
Kekäläinen, Eliisa
Andersson, Noora
Carpén, Olli
Kantonen, Jonas
Mahzabin, Shamita
Myllykangas, Liisa
Mäyränpää, Mikko
Paetau, Anders
Sajantila, Antti
Tynninen, Olli
Source
Medline; PMC
abstract
Published descriptions of the neuropathological features of COVID‐19 patients have been controversial, ranging from only modest or no pathology to severe hypoxic and hemorrhagic phenotypes, thrombotic complications, acute disseminated encephalomyelitis‐like changes, and encephalitis and meningitis. Here we describe the neuropathological findings of four COVID‐19‐positive patients autopsied at the Helsinki University Hospital during the spring of 2020. While three of the patients (age range 63–90) exhibited merely mild to moderate hypoxia‐associated changes, one 38‐year‐old subject with obesity, diabetes (type 2), Parkinson’s disease, and a very severe clinical course was found to have severe ischemic injury, abundant microhemorrhages and enlarged perivascular spaces most pronounced in the white matter and deep gray matter. The pattern of ischemic changes suggested a defect in microcirculation. In addition, a few small perivascular white matter lesions, with macrophages engulfing myelin, were found. No signs of encephalitis or meningitis were detected in any of the patients. When conducting RT‐PCR and immunohistochemical analyses of brain tissue we could not demonstrate in any of the patients marked injury or presence of SARS‐CoV2 in the olfactory epithelium, olfactory bulbs, or brain areas responsible for respiratory control. In conclusion, our small autopsy series demonstrates various hypoxia‐associated neuropathological features in COVID‐19 patients, but no evidence of neurotropism or meningitis/encephalitis.
has issue date
2020-08-06
(
xsd:dateTime
)
bibo:doi
10.1111/bpa.12889
bibo:pmid
32762083
has license
no-cc
sha1sum (hex)
ebe120e89b78a9b23686f48294b5b99dcc08cb60
schema:url
https://doi.org/10.1111/bpa.12889
resource representing a document's title
Neuropathologic features of four autopsied COVID‐19 patients
has PubMed Central identifier
PMC7436498
has PubMed identifier
32762083
schema:publication
Brain Pathol
resource representing a document's body
covid:ebe120e89b78a9b23686f48294b5b99dcc08cb60#body_text
is
schema:about
of
named entity 'Helsinki University'
named entity 'range'
named entity 'defect'
named entity 'mild'
named entity 'patients'
named entity 'DETECTED'
named entity 'PATTERN'
named entity 'DISEASE'
named entity 'OBESITY'
named entity 'SMALL'
named entity 'BRAIN AREAS'
named entity 'DESCRIBE'
named entity 'ABUNDANT'
named entity 'HAVE'
named entity 'PATIENTS'
named entity 'INJURY'
named entity 'HERE'
named entity 'PHENOTYPES'
named entity 'MARKED'
named entity 'OLFACTORY EPITHELIUM'
covid:arg/ebe120e89b78a9b23686f48294b5b99dcc08cb60
named entity 'perivascular'
named entity 'ranging'
named entity 'lesions'
named entity 'perivascular spaces'
named entity 'microcirculation'
named entity 'meningitis'
named entity 'disease'
named entity 'diabetes'
named entity 'immunohistochemical'
named entity 'ischemic injury'
named entity 'respiratory'
named entity 'hemorrhagic'
named entity 'immunohistochemical'
named entity 'brain tissue'
named entity 'thrombotic complications'
named entity 'perivascular'
named entity 'acute disseminated encephalomyelitis'
named entity 'encephalitis'
named entity 'SARS-CoV2'
named entity 'hypoxia'
named entity 'patients'
named entity 'comorbidities'
named entity 'alpha-synuclein'
named entity 'Department of Virology'
named entity 'neuropathological'
named entity 'Olfactory mucosa'
named entity 'diabetes'
named entity 'Helsinki University Hospital'
named entity 'neuropathological'
named entity 'Helsinki University Hospital'
named entity 'encephalitis'
named entity 'SARS-CoV2'
named entity 'pathognomonic'
named entity 'loose stools'
named entity 'extracorporeal membrane oxygenation'
named entity 'gray matter'
named entity 'autopsies'
named entity 'diabetes'
named entity 'Helsinki University Hospital'
named entity 'neurons'
named entity 'neuropathological'
named entity 'ADEM'
named entity 'Finnish'
named entity 'neurological symptoms'
named entity 'brain stem'
named entity 'Finnish'
named entity 'edematous'
named entity 'olfactory bulbs'
named entity 'subendothelial'
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