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  • 1990-1994  (2)
  • Anti-GM2 antibody  (1)
  • Central nervous system (CNS)  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Magnetic resonance imaging of the brain in congenital rubella virus and cytomegalovirus infections (1991)
    Springer
    Neuroradiology 33 (1991), S. 239-242 
    Details
    ISSN: 1432-1920
    Schlagwort(e): Congenital infection ; Cytomegalovirus ; Rubella ; Central nervous system (CNS) ; Magnetic resonance imaging (MRI)
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Two children with congenital rubella virus and six with cytomegalovirus (CMV) infections, were examined by magnetic resonance (MR) and CT. Cranial MR imaging (MRI) with T2-weighted spin-echo (SE) and inversion recovery (IR) sequences demonstrated the following: periventricular hyperintensity (4), subcortical hyperintensity (5), delayed myelination (4), oligo/pachygyria (2), cerebellar hypoplasia (2). This study showed that the more-disabled children had more marked abnormal MRI findings. MRI was more effective in the detection of parenchymal lesion than was CT, although intraventricular calcification was better visualized with CT.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF00588225
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Guillain-Barré syndrome associated with IgM anti-GM1 antibody followingCampylobacter jejuni enteritis (1994)
    Springer
    European journal of pediatrics 153 (1994), S. 181-183 
    Details
    ISSN: 1432-1076
    Schlagwort(e): Guillain-Barré syndrome ; Anti-GM1 antibody ; Anti-GM2 antibody ; Campylobacter jejuni ; HLA-B35
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract We report a 4-year-old girl diagnosed as having Guillain-Barré syndrome after infection by Penner serotype 19 ofCampylobacter jejuni. The patient had the HLA-B35 antigen. Neurological examination revealed distal-dominant weakness and intact sensation. Serial electrophysiological studies indicated that the predominant process was axonal degeneration involving motor nerves. An enzyme-linked immunosorbent assay revealed the presence of high titres of serum IgM antibodies to gangliosides GM1 and GM2. The IgM auto-antibody titres decreased concurrently with the clinical course of the illness and no switching from IgM to IgG secretion took place.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF01958981
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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    Artikel (Nationallizenzen)
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