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  • 1
    Electronic Resource
    Electronic Resource
    Diagnosis of neurinoma in the region of the jugular foramen — a case report (1987)
    Springer
    Neurosurgical review 10 (1987), S. 41-46 
    Details
    ISSN: 1437-2320
    Keywords: Collet-Sicard syndrome ; hypoglossal nerve ; jugular foramen ; neurinoma ; Vernet's paralysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Neurinomas in the region of the jugular foramen are extremely rare, are difficult to diagnose before surgery, and have seldom been described in the literature. The typical jugular foramen syndromes (Collet-Sicard syndrome, Vernet's paralysis) may be caused by many various disorders. The diagnostic problems are illustrated using one of our cases as an example. The differential diagnosis was made before surgery using currently available radiologic techniques. The tentative diagnosis “neurinoma of the hypoglossal nerve” was confirmed intraoperatively and histologically.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01780593
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Ungewöhnliche Morphologie beim Leigh-Syndrom (2000)
    Springer
    Klinische Neuroradiologie 10 (2000), S. 13-17 
    Details
    ISSN: 1615-6706
    Keywords: Schlüsselwörter: Leigh-Syndrom ; MRT ; Pathologisch-anatomische Befunde ; Key Words: Leigh syndrome ; MRI ; Patho-histological findings
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Abstract: We report on 3 children suffering from Leigh syndrome as diagnosed on clinical and laboratory results. In each child there were some deviations from the reported typical morphological picture on MRI. However, the lesions reported here fit very well to the patho-histological findings in Leigh syndrome.
    Notes: Zusammenfassung: Wir beschreiben drei Kinder, bei denen klinisch und laborchemisch ein Leigh-Syndrom diagnostiziert wurde. Bei jedem dieser Kinder lagen in der Bildgebung unterschiedliche Abweichungen von den typischen, bisher beim Leigh-Syndrom berichteten Läsionen in der MRT vor. Die gefundenen Veränderungen in der MRT passen allerdings sehr gut zu den pathologisch-anatomischen Befunden bei dieser Erkrankung.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
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