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  • Articles: DFG German National Licenses  (5)
  • Embolisation  (3)
  • Autoimmune diseases  (1)
  • Carbamazepine  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 67 (1989), S. 967-970 
    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
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  • 2
    ISSN: 1433-0407
    Keywords: Schlüsselwörter Aneurysma ; Transkranielle Duplexsonographie ; Embolisation ; Subarachnoidalblutung ; Key words Aneurysm ; Transcranial Duplex sonography ; Coil embolization ; Subarachnoid hemorrhage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary We investigated 88 Patients with a total of 102 angiographically diagnosed intracranial aneurysms by means of transcranial colour coded Duplex sonography (TCCD) during a time period of 15 months. Both the size and teh localization of teh aneuryms were determined. Seventy aneurysms (77%) with a diameter of 16±8 mm (6-55mm) were detectable, with excellent visualization in 36 (42%), moderate visualization in 34 (40%), and no sufficient visualization in 16 (16%) aneurysms, respectively. In another 16 cases (16%) there was no sufficient vone window. Thrombotic material inside the aneurysm was detectable in 16/20 cases (75%), visualization of coil embolized aneurysms in 12/25 patients (48%). TCCD allows the follow up of cerebral aneurysms, with the detection of thrombosis and treatment effects after embolization. The method is not valid for the detection of intracranial aneurysms
    Notes: Zusammenfassung Innerhalb eines Zeitraumes von 15 Monaten wurden 88 Patienten mit 102 angiographisch nachgewiesenen intrakraniellen Aneurysmen unter Verwendung einer 2-MHz-Sonde mit der transkraniellen farbkodierten Duplexsonographie (TCCD) untersucht. Es wurden die Größe und der genaue Aneurysmasitz bestimmmt. Insgesamt konnten 70 (77%) Aneurysmen mit einem Durchmesser von 16±8 mm (6–55 mm) dargestellt werden. Eine sehr gute Darstellung der Aneurysmen gelang bei 36 (42%), eine mäßige bei 34 (40%) Aneurysmen, 16 (16%) Aneurysmen konnten trotz ausreichender Bildqualität nicht dargestellt werden. Bei weiteren 16 (16%) Aneurysmen war kein ausreichendes Knochenfenster vorhanden. Thrombosierte Anteile innerhalb der Aneurysmen konnten bei 16 (75%) von 20, der mit Coils behandelte Anteil bei 12 (48%) von 25 Aneurysmen erfolgreich dokumentiert werden. Die Methode ist zum Nachweis von teilthrombosierten Anteilen, von Behandlungserfolgen nach Coilembolisation und zur Verlaufskontrolle nicht behandelbarer Aneurysmen geeignet. Die Darstellbarkeit kleiner Aneurysmen ist begrenzt durch das Auflösungsvermögen und die teilweise ungünstigen Beschallungswinkel, somit eignet sich die TCCD nicht als Screeningmethode zum Nachweis von Aneurysmen.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1920
    Keywords: Key words Aneurysm ; Transcranial colour-coded duplex sonography ; Embolisation ; Subarachnoid haemorrhage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We examined 72 patients with 89 angiographically confirmed intracranial aneurysms, using transcranial colour-coded duplex sonography (TCCD) to determine the location and size of the aneurysm. The patients were admitted for coil embolisation of their aneurysm following subarachnoid haemorrhage or because of a cranial nerve palsy. Using a 2/2.25 MHz transducer, 42 aneurysms (47 %) were seen satisfactorily through the temporal bone window or foramen magnum. In 24 cases (27 %) image quality was insufficient as a result of a poor bone window, of the aneurysm having a diameter of less than 6 mm or of its being in an unfavourable location. In 23 other cases (26 %) it was not possible to detect the aneurysm. Thrombosed structures could be demonstrated using TCCD in 8 of 12 giant intracavernous or basilar artery aneurysms, and in 15 of 19 aneurysms treated by platinum coil embolisation. TCCD offers a noninvasive method for monitoring progressive intra-aneurysmal thrombosis following coil embolisation and for follow-up of patients with untreatable fusiform aneurysms, should this be required. Detection of small aneurysms is limited by spatial resolution and insonation angles.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1920
    Keywords: Aneurysm ; Transcranial colour-coded duplex sonography ; Embolisation ; Subarachnoid haemorrhage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We examined 72 patients with 89 angiographically confirmed intracranial aneurysms, using transcranial colour-coded duplex sonography (TCCD) to determine the location and size of the aneurysm. The patients were admitted for coil embolisation of their aneurysm following subarachnoid haemorrhage or because of a cranial nerve palsy. Using a 2/2.25 MHz transducer, 42 aneurysms (47%) were seen satisfactorily through the temporal bone window or foramen magnum. In 24 cases (27%) image quality was insufficient as a result of a poor bone window, of the aneurysm having a diameter of less than 6 mm or of its being in an unfavourable location. In 23 other cases (26%) it was not possible to detect the aneurysm. Thrombosed structures could be demonstrated using TCCD in 8 of 12 giant intracavernous or basilar artery aneurysms, and in 15 of 19 aneurysms treated by platinum coil embolisation. TCCD offers a noninvasive method for monitoring progressive intra-aneurysmal thrombosis following coil embolisation and for follow-up of patients with untreatable fusiform aeurysms, should this be required. Detection of small aneurysms is limited by spatial resolution and insonation angles.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neurology 230 (1983), S. 193-196 
    ISSN: 1432-1459
    Keywords: Arginine vasopressin ; Carbamazepine ; Anticonvulsants ; Epilepsy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Bei 112 unter Monotherapie mit Carbamazepin, Phenytoin, Primidon oder Valproat stehenden erwachsenen Anfallskranken sowie bei 19 gleichaltrigen Kontrollpersonen wurden radioimmunologisch die Vasopressin-Plasma-Konzentrationen bestimmt. Es wurden keine signifikanten Unterschiede zwischen den Gruppen gefunden. Einige der mit Carbamazepin und Primidon monotherapierten Epileptiker wiesen niedrige Vasopressin-Werte auf. Die Carbamazepin-Serumspiegel korrelierten nicht mit den Vasopressin-Konzentrationen. Somit ergab sich weder ein Hinweis auf eine vermehrte Vasopressin-Ausschüttung unter Langzeittherapie mit Carbamazepin noch eine besondere Hemmung der Ausschüttung durch Phenytoin.
    Notes: Summary Plasma arginine vasopressin concentrations were determined by radio-immunoassay in 112 adult epileptics who were taking carbamazepine, phenytoin, primidone, or sodium valproate in long-term monotherapy, and in 19 controls. No significant difference was found between the groups, but some epileptics taking carbamazepine and primidone showed low values. Serum concentrations of carbamazepine did not correlate with the concentrations of plasma arginine vasopressin. In conclusion, there was no evidence of a stimulating effect of chronic carbamazepine medication or a special inhibiting effect of phenytoin on the release of vasopressin arginine from the posterior pituitary.
    Type of Medium: Electronic Resource
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