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  • 1
    Electronic Resource
    Electronic Resource
    Immunoglobulin therapy in neurologic diseases (1989)
    Springer
    Journal of molecular medicine 67 (1989), S. 967-970 
    Details
    ISSN: 1432-1440
    Keywords: Immunoglobulins ; Autoimmune diseases ; Encephalitis ; Myasthenia gravis ; Guillain-Barré syndrome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary An overview is given on the use of immunoglobulins in clinical neurology. While 5S-immunoglobulins may be employed in addition to virostatics in viral encephalitis, 7S-immunoglobulins can be used in autoimmune diseases like myasthenia gravis, multiple sclerosis, and the Guillain-Barré syndrome. Refractory childhood epilepsies like the Lennox-Gastaut syndrome responded to 7S-immunoglobulins. Hyperimmunoglobulins are to be given in bacterial infections in which toxins are formed and in viral infections caused by cytomegalovirus and tick-borne encephalitis virus. While some open studies report benefit from the use of immunoglobulins in neurological diseases, controlled evidence for their efficacy is still missing.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01716058
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    The heart in muscular dystrophy: An electrocardiographic and ultrasound study of 20 patients (1991)
    Springer
    European archives of psychiatry and clinical neuroscience 241 (1991), S. 177-180 
    Details
    ISSN: 1433-8491
    Keywords: Muscular dystrophy ; Cardiomyopathy ; Myotonic dystrophy ; Heart disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Twenty patients with different types of muscular dystrophy (MD) were included in a cross-sectional study by means of electrocardiography and ultrasound cardiography. A manifest cardiomyopathy was detected in 8 patients; a latent cardiomyopathy was found in 4. A hypertrophic cardiomyopathy was especially frequent in facioscapulohumeral MD, a congestive cardiomyopathy in Becker-Kiener MD. The ECG showed a reduction in the QT interval and frequent block formers in the X-chromosomal inherited forms and the trunc-girdle form. Bradycardia and a prolonged QT interval were frequent in myotonic dystrophy and facioscapulohumeral MD. Signs of cardiac infarction in the ECG were most frequent in the trunc-girdle forms. A high cardiac output per minute in conjuction with increased left ventricular volume was frequent in Becker-Kiener, and Landouzy MD. A left ventricular dysfunction with reduced ejection was characteristic of myotonic dystrophy and truncgirdle MD. A mitral valve prolapse was more frequent with increasing severity of the muscle disease and was particularly frequent in myotonic dystrophic and Landouzy MD. The cardiac output per minute and the stroke volume were significantly lower (P≤0.03) where a mitral valve prolapse was present.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02219718
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
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