Search Results - "LEICHER, C. R"
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Autosomal dominant Emery-Dreifuss dystrophy due to mutations in rod domain of the lamin A/C gene
Published in Neurology (25-07-2000)“…Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and…”
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Hereditary neuropathy with liability to pressure palsies in children
Published in Pediatric neurology (01-11-1999)“…The clinical and neurophysiologic findings of two children presenting with focal weakness and atrophy in unusual nerve distributions and no apparent antecedent…”
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Neurologic manifestations of Schoenlein-Henoch purpura: report of three cases and review of the literature
Published in Pediatrics (Evanston) (01-04-1985)“…Three patients developed prominent neurologic symptoms and signs associated with Schoenlein-Henoch purpura. A 7 1/2-year-old boy was seen with status…”
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Focal cerebral deficits in severe hypomagnesemia
Published in Pediatric neurology (01-09-1991)“…Hypomagnesemia has been associated with multiple neurologic abnormalities, including irritability, seizures, paralysis, and choreiform movements. A patient…”
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A Case of Infant Botulism in New England
Published in The Journal of infectious diseases (01-03-1984)“…Since 1975, over 300 cases of infant botulism have been reported to the Centers for Disease Control. These cases have occurred throughout the United States…”
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Termination of nutrition and hydration in a child with vegetative state
Published in Archives of pediatrics & adolescent medicine (01-01-1994)“…A child in a vegetative state may present difficult decisions for physicians and families regarding the course of treatment. We report a case of a child who…”
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Child neurologist as expert witness: a report of the Ethics and Practice Committees of the Child Neurology Society
Published in Journal of child neurology (01-08-1998)“…A questionnaire was circulated to 1126 members of the Child Neurology Society to assess their opinions regarding the current medical-legal system and to…”
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