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  • 1
    ISSN: 1546-170X
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] Ischemic peripheral neuropathy is a frequent, irreversible complication of lower extremity vascular insufficiency. We investigated whether ischemic peripheral neuropathy could be prevented and/or reversed by gene transfer of an endothelial cell mitogen designed to promote therapeutic ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 95 (1998), S. 213-216 
    ISSN: 1432-0533
    Keywords: Key words Cerebral amyloid angiopathy ; Lobar cerebral hemorrhage ; Down’s syndrome ; Alzheimer’s disease ; Hereditary cerebral hemorrhage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Cerebral amyloid angiopathy (CAA) is an important cause of spontaneous intracerebral hemorrhages in the elderly and is often seen in the brains of patients with Alzheimer’s disease, Down’s syndrome (DS), and hereditary cerebral hemorrhage with amyloidosis of the Dutch type. We report two patients with DS and extensive CAA who died of intracerebral hemorrhage; only two other such case reports exist in the literature. We believe the incidence of such cases is higher than is reported and that the likelihood of hemorrhage in the setting of CAA is independent of the patient’s underlying disease.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 29 (1974), S. 93-97 
    ISSN: 1432-0533
    Keywords: Dissecting Aneurysm ; Carotid Artery ; Moya-Moya
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We present clinical and pathologic data on a 14-year-old boy with bilateral dissecting aneurysms of the internal carotid and middle cerebral arteries. The case is unusual in that bilateral dissecting aneurysms of the intracranial vessels have not been described, and because the internal elastic lamina was focally absent in both intracranial and somatic arteries. This abnormality of the elastica has been described in association with internal carotid occlusion and telangiectasia of the basal ganglia, the moya-moya syndrome. The relation between dissecting carotid aneurysms and moya-moya is discussed.
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  • 4
    ISSN: 1573-7373
    Keywords: seizures ; epilepsy ; children ; brain tumors ; astrocytoma ; medulloblastoma ; ependymoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We examined potential clinical and pathologic correlates of seizures among the 3,291 children in the Childhood Brain Tumor Consortium database. Fourteen percent had seizures prior to their hospitalization for a brain tumor. Among children who had a supratentorial tumor, seizures occurred in 22% of those less than 14 years of age. The prevalence of seizures increased to 68% of older teenagers. Among children with an infratentorial tumor, the prevalence of seizures was relatively constant at 6% over all age groups. The onset of seizures began more than one year prior to surgical tumor removal in over half of the children aged five or more with supratentorial tumors, significantly longer than for those of the same age with infratentorial tumors. Almost all children (98.9%) with an infratentorial tumor and seizures had at least one other symptom and more than three-fourths of them had at least three. Eighty-nine percent of children with a supratentorial tumor and seizures had at least one other symptom and more than one-half had at least three symptoms. Regardless of whether the tumor was above or below the tentorium, confusion or stupor and coma were more common in children with seizures than in children without seizures. Among children with supratentorial tumors, symptoms of a declining academic performance or an abnormality of personality, speech, walking, or sensation were significantly more frequent in children with seizures, while visual symptoms (other than visual loss or diplopia) and nausea or vomiting were less frequent. Among children with supratentorial tumors, those who had seizures were more likely to have paralysis of an arm, hand, or face, confusion or stupor, or coma and less likely to exhibit irritability, papilledema, optic atrophy, decreased visual acuity, pupillary abnormalities, or abducens paresis. Among children with infratentorial tumors, those with seizures were significantly less likely to have truncal ataxia, but more likely to experience confusion.
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