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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 55 (1982), S. 309-315 
    ISSN: 1435-1463
    Keywords: Hepatic coma ; L-valine binding ; branched chain amino acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Serotonin (5-HT) receptors are modulated by L-valine (VAL). For further characterization of this effect a binding assay of [14C]-L-VAL has been developed. A brief description of the experimental conditions is given. Moreover, measurement of VAL-binding has been applied to human brain tissue either from controls or hepatic failure. A marked increase of VAL-binding sites with no change in affinity was noted in hepatic coma, while in patients treated with parenteral nutrition plus VAL no such change could be measured. It is concluded that the beneficial therapeutic effects of VAL in hepatic encephalopathy are, at least in part, due to its modulating action on post-synaptic receptor membranes.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 51 (1981), S. 113-122 
    ISSN: 1435-1463
    Keywords: Parkinson's disease ; serotonin receptors ; receptor binding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Crude membrane preparations from the frontal cortex of controls and parkinsonian patients were used to demonstrate affinity changes of the specific3H-5-hydroxytryptamine (5-HT) binding sites. Two such sites were noteable in controls, a finding consistent with earlier observations. In Parkinson's disease, both high- and low-affinity sites are significantly decreased. Additional experiments either with prolonged incubation times or pre-incubation with N-ethylmaleimide change the two affinities to a single high-affinity or low-affinity constant. The concept of transitional states of 5-HT receptors is discussed and seems to have important implications in the treatment of parkinsonism.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 54 (1982), S. 171-179 
    ISSN: 1435-1463
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Antigens immunochemically related to rat brain D2-protein and D 3-protein were measured by crossed immunoelectrophoresis in human putamen extracts. 10 patients with Parkinson's disease were compared with 10 controls. No difference was found between the specific concentration of the D 2-like and the D 3-like antigens in the two groups. This was taken as indicative for the absence of both major neuronal degeneration and ongoing synaptic remodelling in putamen of Parkinson's disease patients.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0533
    Keywords: Holoprosencephaly ; Callosal defect ; Malformations ; Craniofacial dysplasias
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Review of 28 autopsy cases of holoprosencephaly (HPE) and 50 cases of agenesis of corpus callosum (ACC) (16 complete and 34 partial) revealed a high incidence of associated abnormalities in both the CNS and other organs. Craniofacial dysplasias were present in 92.8% of the HPE and in 37.8% of the cases with ACC; most frequent were microcephaly, hypotelorism, hypertelorism, and cleft formations. Associated CNS malformations were present in 93% of the cases of HPE and in 88% of those with ACC. In HPE except for constant defects of the forebrain commissures, the most frequent anomalies are migration disorders (95%), displaced hippocampus (85%) and fusion of the basal ganglia (65%) not seen in “arhinencephaly” (olfactory aplasia without failure of prosencephalic cleavage) except for occasional synthalamus. Less frequent were hydrocephalus (61%), lobar hypoplasia, porencephaly, arachnoid cysts, vascular malformations, and dysraphic lesions. Associated anomalies in ACC are Probst's longitudinal bundle (64%), hydrocephalus (44%), microcephaly and dysgyrias (38% each), rhinencephalic defects (32%), absence of forebrain commissures and other dysraphic changes, lobar hypoplasias and arachnoid cysts (12% each), and rare instances of cerebellar and brainstem dysplasia, optic nerve and tract anomalies, encephalocele and choroid plexus lesions. Non-nervous system malformations include a wide variety of musculoskeletal defects (35.8 and 25%), genitourinary (32.1 and 22.7%), cardiovascular (28.5 and 20.5%), gastrointestinal (39.5 and 9.5%), and other organ abnormalities. Comparison of these observations with the data from the literature emphasize the heterogeneity of associated malformations in telencephalic midline defects which show no consistent pattern except for craniofacial anomalies, microcephaly, hydrocephalus, and frequent migration disorders of the CBS.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0584
    Keywords: Granulocyte transfusion ; Graft-versus-Host reaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Fatal Graft-versus-Host reactions (GVHR) were observed in a 5-year-old boy with Hodgkin's disease after application of non irradiated granulocytes derived from his mother and in a 59 year old female suffering from glioblastoma following transfusion of buffy coat cells from fresh blood units. Clinical signs as well as histopathological changes found in skin biopsies and subsequently at autopsy, were typical for GVHR. In one of the cases the sex difference between donor and recipient provided evidence for engraftment of donor lymphocytes.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 65 (1984), S. 168-171 
    ISSN: 1432-0533
    Keywords: Metastasis ; Extraocular muscle ; Solid tumors ; Orbital metastases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Three autopsy cases with discrete metastatic involvement of one or several extraocular orbital muscles by disseminated amelanotic melanoma (one case) and lobular mammary adenocarcinoma (two cases) associated with extensive meningeal involvement are reported. Clinical ocular symptoms including pain, exophthalamus, and diplopia occurred 6 months to almost 5 years after resection of the primary tumor; in two cases CT scan showed spindle-like enlargement of orbital mucles. Pathologic examination disclosed solid localized metastatic deposits in several extraocular muscles of one (breast carcinomas) or both orbits (melanoma), with diffuse invasion of striated muscle, but without necrosis, inflammation, or involvement of other orbital adnexa, eye ball, optic nerves, or orbital bone. Since no continous invasion of orbital or intraocular structures by diffuse meningeal blastomatosis was histologically observed, rare metastatic involvement of extraocular muscles via hematogenic route is suggested.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0942-0940
    Keywords: Cerebral cysts ; malignant gliomas ; multimodality treatment ; radiation necrosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Eight cases of cerebral cyst formation among 50 patients (= 16%) with malignant supratentorial gliomas treated by surgery, megavoltage radiation, and multiple-agent chemotherapy are reported. Five of them developed signs of intracranial hypertension or progressive neurological deficit, while in three patients cerebral cysts were detected by CT without clinical deterioration. At operation or autopsy, or both, the large fluid-filled, smooth-walled cysts were lined by glio-mesenchymal scar tissue with no or little tumour recurrence in five, while three patients showed large recurrent tumour masses associated with necrosis and cyst formation. Clinical signs or CT evidence, or both, of cerebral cysts developed 4 to 12 months (average 10 months) after the first craniotomy, and 3 to 9 months after termination of radiotherapy, usually after the second to fourth course of polychemotherapy. The cystic cavities which are attributed to increased necrosis and other effects of radiation and cytostatic treatment, may mimic tumour progression or recurrence, and cerebral abscess, but are usually recognized by CT. Surgical treatment produced transient clinical improvement in 5 patients, but usually did not prevent the fatal outcome of the disease, which in these patients occurred 3 weeks to 6 months after surgical treatment of cyst formation, their life span ranging from 9 to 22 months. The pathogenesis and clinical problems related to cerebral cysts arising following multimodality treatment of malignant brain tumours are discussed.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Acta neurochirurgica 58 (1981), S. 121-126 
    ISSN: 0942-0940
    Keywords: Intramedullary tumour ; giant-cell glioblastoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A case of giant-cell glioblastoma occurring in the upper thoracic cord of a male aged 76 without evidence of intracranial lesion is reported. Partial tumour resection with decompression and radiotherapy did not improve the patient's neurological deficit.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-1459
    Keywords: Tuberculous meningitis ; Midbrain syndrome ; Bulbarbrain syndrome ; Apallic syndrome ; Specific vasculitis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es wird über 7 Fälle einer schwersten Verlaufsform der Meningitis tuberculosa berichtet, bei denen sich ein Mittelhirnsyndrom entwickelt hat. Es ließen sich 2 bzw. 3 Verlaufsformen trennen. Bei der ersten Gruppe stand die exsudative Entzündung mit Hirnödem im Vordergrund und dadurch eine relativ rasche Entwicklung zum Vollbild des akuten Mittelhirnsyndroms, das in ein Bulbärhirnsyndrom übergehen kann. Bei der zweiten Gruppe zeigte sich eine protrahierte Entwicklung des Mittelhirnsyndroms mit Übergang in ein apallisches Syndrom und morphologisch eine lokale Zwischenhirn- und Mittelhirnschädigung durch Einklemmung und spezifische Vaskulitis bzw. Gefäßkompression. Die dritte Gruppe wies neben der lokalen Mittelhirnsymptomatik, die sich nie bis zum Vollbild verstärkte, eine diffuse Großhirnstörung in einem Desintegrationsverlauf auf. Aus den Verlaufsbeobachtungen ergibt sich, daß die spät einsetzende Diagnose mit verzögertem Therapiebeginn für die schwerste Verlaufsform der Meningitis tuberculosa von entscheidender Bedeutung ist.
    Notes: Summary Seven cases of the most severe form of tuberculous meningitis, in which a midbrain syndrome developed, are reported. Three different types of progress were observed. Exudative inflammation and cerebral edema dominated in the first group, causing the rapid development of the acute midbrain syndrome, which may turn into a bulbar syndrome. In the second group the development of the midbrain syndrome was delayed and an apallic syndrome followed. The morphological examination disclosed local diencephalic and midbrain lesions caused by herniation and specific vasculitis and vascular compression. The third group showed disintegration of cortical function as a result of parenchymal lesions, apart from local midbrain symptoms which never fully intensified into the midbrain syndrome. Observation of the progress of the disease proved that late diagnosis and delayed therapy were decisive in cases of the most severe form of tuberculous meningitis.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neurology 231 (1984), S. 38-42 
    ISSN: 1432-1459
    Keywords: Granulomatous angiitis ; Nervous system ; Giant cell arteriitis ; Vasculitis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es wird über einen Fall von zerebraler granulomatöser Angiitis des linken Schläfenlappens berichtet, der zunächst für einen Hirntumor gehalten wurde. Nach der operativen Entfernung von gliomatös anmutendem Gewebe wurde histologisch die Diagnose einer granulomatösen Vaskulitis gestellt. Medikamentös wurde lediglich Dexamethason in fallender Dosierung während der ersten fünf postoperativen Tage verabreicht. Auf klinische und morphologische Unterschiede zu bisher publizierten Fällen von granulomatöser Angiitis des Nervensystems wird näher eingegangen.
    Notes: Summary A case of cerebral granulomatous angiitis of the left temporal lobe mimicking a brain tumour is presented. Following surgical removal of a glioma-imitating mass, histological examination disclosed a granulomatous vasculitis. Treatment consisted of dexamethasone given in tapering doses for 5 days after surgery. Clinical and morphological differences from other reported cases of granulomatous angiitis of the nervous system are described.
    Type of Medium: Electronic Resource
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