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  • Acquired arrhythmia  (1)
  • Chronic intracerebral and intracerebellar hematoma  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Chronic encapsulated hematomas in the brain (1985)
    Springer
    Acta neuropathologica 66 (1985), S. 24-28 
    Details
    ISSN: 1432-0533
    Keywords: Chronic intracerebral and intracerebellar hematoma ; Fibrous capsule ; Small vascular malformation ; Encapsulated mass lesion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Two cases, one of a chronic encapsulated intracerebral hematoma occuring in a 43-year-old man and the other of an intracerebellar hematoma in an 8-year-old boy, are reported. In both cases CT scans revealed an encapsulated lesion containing the hematoma, but angiographic pictures were poor except for revealing a space-occupying lesion and a small vascular lesion. Both hematomas were successfully removed. Each case was associated with a thick, fibrous capsule that was found histologically to arise from an occult angiomatous malformation. The encapsulated hematomas partially included old thromboses, and both old and recent areas of hemorrhage. The latter were considered to be due to the rupture of vessels developed near the inner surface of the thickest part of the fibrous capsule. Although the condition is uncommon, chronic hematoma must be considered when encapsulated mass lesion is present in the brain.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00698291
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population (2000)
    Springer
    Journal of human genetics 45 (2000), S. 182-183 
    Details
    ISSN: 1435-232X
    Keywords: Key words Long QT syndrome ; Single nucleotide polymorphism ; Japanese population ; Acquired arrhythmia ; Proarrhythmia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract We report here 20 single nucleotide polymorphisms (SNPs), including 10 novel ones, and their allelic frequencies detected in four genes that are known to be responsible for familial long QT syndrome in the Japanese population; 7 polymorphisms are in the KCNQ1 gene, 6 in the KCNH2 gene, 5 in the SCN5A gene, and 2 in the KCNE1 gene. These data will be of use for genetic association studies of acquired cardiac arrhythmias.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s100380050207
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
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