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  • 1
    Electronic Resource
    Electronic Resource
    Moyamoya disease with a developmental anomaly of the mesenchyme (1985)
    Springer
    European journal of pediatrics 144 (1985), S. 93-95 
    Details
    ISSN: 1432-1076
    Keywords: Moyamoya disease ; Arterial occlusive disease ; Short stature ; Syndactylia ; Cerebrovascular circulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We treated a Japanese boy with moyamoya disease accompanied by synbrachydactylia, funnel chest, pes equinus and short stature. Angiograms showed the anomalous origin of the occipital artery in addition to the moyamoya vascular network at the base of the brain. A generalised mesenchymal anomaly was suggested in this case.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00491940
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Magnetic resonance imaging of jugular foramen neurinomas (1989)
    Springer
    Acta neurochirurgica 96 (1989), S. 83-87 
    Details
    ISSN: 0942-0940
    Keywords: Jugular foramen neurinoma ; magnetic resonance imaging ; computed tomography ; surgical anatomy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Four cases of jugular foramen neurinoma, extending from the posterior fossa into the temporal bone through the jugular foramen, are reported. The information provided by magnetic resonance imaging was compared with that by computed tomography. Due to the excellent sensitivity, the absence of bone artifacts, and the ease of imaging in any plane, magnetic resonance imaging gave better information particularly about the location of the tumour than X-CT scan did. It included the dumb-bell-shaped tumour through the jugular foramen, the extra-axial nature of the tumour, and the precise anatomical relationships between the tumour and the facial and acoustic nerves or the internal carotid artery. Sagittal and coronal views clearly demonstrated the superior and inferior margins of the tumour. The information is very useful not only for preoperative diagnosis but also for planning the surgical approaches and postoperative follow-up.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01456163
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Surgical treatment for paediatric patients with moyamoya disease by indirect revascularization procedures (EDAS, EMS, EMAS) (1989)
    Springer
    Acta neurochirurgica 98 (1989), S. 135-140 
    Details
    ISSN: 0942-0940
    Keywords: Moyamoya disease ; paediatric case ; surgical treatment ; indirect non-anastomotic EC-IC bypass
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Surgical results of paediatric patients with Moyamoya disease who were treated by indirect revascularization procedures are reported. Encephalo-duro-arterio-synangiosis (EDAS), encephalomyo-arterio-synangiosis (EMAS), and/or encephalo-myo-synangiosis (EMS) were performed on 47 sides of 29 children with Moyamoya disease. The results of those non-anastomotic EC-IC bypass procedures were evaluated clinically, angiographically, and by computed tomography (CT). Postoperative external carotid angiograms showed a good collateral formation through EDAS, EMAS, or EMS in about 70–80 percent of all surgically treated sides. The symptoms such as TIA, RIND, and/or involuntary movements disappeared in the cases with a good collateral formation but not in those with insufficient development of the collateral circulation. The indirect EC-IC bypass surgery seems effective for most of the children with Moyamoya disease who present with ischaemic signs.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01407339
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  • 4
    Electronic Resource
    Electronic Resource
    Balloon test occlusion of the internal carotid artery with monitoring of compressed spectral arrays (CSAs) of electroencephalogram (1989)
    Springer
    Acta neurochirurgica 101 (1989), S. 29-34 
    Details
    ISSN: 0942-0940
    Keywords: Balloon test occlusion ; internal carotid artery ; compressed spectral arrays (CSAs): electroencephalography (EEG) ; Matas test
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We used the compressed spectral arrays (CSAs) of the electroencephalogram (EEG) to monitor cerebral blood flow related events in balloon test occlusion of the internal carotid artery (balloon Matas test). Reliability of the CSAs was examined in 22 patients subjected to the test. Of 9 patients who underwent subsequent permanent carotid occlusion, in 6 there was no change on CSAs and/or in neurological conditions. In 2 patients, there was a slowing on CSAs prior to the appearance of neurological deterioration during clinical testing. CSAs transformed these EEG changes into a succinct graphic display. In 1 of the 2, for whom the Matas test was repeated 1 year later, there was a change from positive to negative and delayed cerebral infarction occurred after carotid occlusion. In the other patient, an ischaemic insult occurred during the balloon occlusive procedures. The third patient had a fatal delayed ischaemic complication 3 days after surgical ligation of the cervical carotid artery, despite the negative balloon Matas test. Complications in these 3 patients were presumably related to thromboembolic mechanisms. The balloon Matas test monitored by CSAs is useful for detecting change in brain functions attributed to an inadequate blood flow. However, this test is unreliable for predicting thrombo-embolic complications.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01410065
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  • 5
    Electronic Resource
    Electronic Resource
    Radiological analysis of hemifacial spasm with special reference to angiographic manifestations (1986)
    Springer
    Neuroradiology 28 (1986), S. 288-295 
    Details
    ISSN: 1432-1920
    Keywords: ‘Essential’ hemifacial spasm ; Microsurgical neurovascular decompression ; Vertebral angiogram ; AICA ; PICA ; Redundant vertebral artery
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Fifty-one patients with hemifacial spasm secondary to facial nerve compression by normal appearing, elongated, tortuous and/or dilated arteries, were treated by microsurgical neurovascular decompression. Post-operatively, 91% of 44 of these patients with one to six year postoperative follow-ups were satisfactory. The angiographic findings showed significant increase in the number of common trunk anomalies. Variations of the anterior and posterior inferior cerebellar and vertebral arteries are discussed in relation to nerve compression.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00333433
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    Paper (German National Licenses)
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  • 6
    Electronic Resource
    Electronic Resource
    Computed tomography and angiography in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes); report of 3 cases (1987)
    Springer
    Neuroradiology 29 (1987), S. 393-397 
    Details
    ISSN: 1432-1920
    Keywords: Mitochondrial encephalomyopathy ; MELAS ; Computed tomography ; Angiography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Among mitochondrial encephalomyopathies, MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes, Pavlakis et al. 1983) is recognized as a distinct syndrome characterized by generalized convulsions and recurrent stroke-like episodes. The neuroradiological findings of three patients with MELAS are reported here. Retrospective review shows that MELAS should be included in the differential diagnosis of infarct-like lesions of the cerebrum.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00348922
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  • 7
    Electronic Resource
    Electronic Resource
    Isolated unilateral absence of left pulmonary artery with peribronchial arteriovenous malformation showing recurrent hemoptysis (1987)
    Springer
    Pediatric radiology 17 (1987), S. 316-318 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Unilateral absence of a pulmonary artery is an uncommon condition and usually complicated by a cardiac anomaly. Our case is a rare one who showed the absence of the left pulmonary artery with left aortic arch and without cardiac anomaly. He suffered from recurrent hemoptysis and pneumonia since he was 9 months old. Angiography revealed peribronchial arteriovenous malformation of the affected lung which was supplied from subclavicular arteries and bronchial arteries. Although he was treated by operative ligation and angiographic embolotherapy of the supplying systemic arteries, the repeated the attacks of massive hemoptysis and necessiated left pneumonectomy at 10 years of age.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02388246
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