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Creutzfeldt-Jakob disease and cerebral amyloid angiopathy
An 83-year-old female with no personal or familial neurological history developed progressive gait and speech disturbance and left motor deficit. She suffered intractable seizures and died 3 months after the o...
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Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain
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Abstracts
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Lyme disease presenting as a stroke in the vertebrobasilar territory: MRI
A 28-year-old female farmer, without vascular risk factors, developed a limited infarct of the pons, associated with a lymphocytic cerebrospial fluid (CSF) pleocytosis. Titres of specific antibodies againstBorrel...
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Atypical MR presentation of Wilson disease: a possible consequence of paramagnetic effect of copper?
A 53-year-old patient with Wilsons's disease and without autonomic dysfunction presented on T2-weighted MR study an atypical decreased signal intensity of the putamina and the caudate nuclei. Possible explanat...
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Muscle mitochondrial DNA in encephalomyopathy and ragged red fibres: a Southern blot analysis and literature review
Various mitochondrial DNA abnormalities have been described in patients with encephalomyopathies. We performed Southern blot analysis of skeletal muscle mitochondrial DNA in nine adult patients with clinical f...
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Extensive form of progressive multifocal leucoencephalopathy associated with laryngeal carcinoma
A case is reported of the rare association between progressive multifocal leucoencephalopathy and carcinoma. A 66-year-old man underwent a laryngectomy for carcinoma. Four years later he developed a local recu...
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Monstrocellular heavily lipidized malignant glioma
A man of 32 years was admitted with a 3-month history of temporal lobe epilepsy. CT-Scan showed a well-circumscribed area of heterogenous contrast enhancement in the right temporal lobe. Gross total resection ...
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Parkinsonian syndrome and central nervous system lymphoma involving the substantia nigra
The clinical history and postmortem neuropathologic findings of a case of cerebral lymphoma revealed by a typical parkinsonian syndrome are reported. The clinical symptoms initially improved with dopa therapy....
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Luyso-pallido-nigral atrophy and amyotrophic lateral sclerosis
The clinical and pathologic findings in a 34-year-old woman with basal ganglia degeneration and amyotrophic lateral sclerosis are reported. The duration of symptoms was 2 years. A maternal uncle had a parkinso...