Development of encephalopathic features similar to Reye syndrome in rabbits.
نویسندگان
چکیده
منابع مشابه
Reye syndrome and salicylates.
This year in the United States there has been considerable controversy about circumstantial evidence linking salicylates to the pathogenesis of Reye syndrome and, in particular, whether that evidence is sufficiently strong to justify action. After careful review both the Federal government and the American Academy of Pediatrics have warned physicians and parents of the possible risk of Reye syn...
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اشعار ریچ، به عنوان اشعاری که همیشه در حال تغییر و دگرگونی هستند، تجسمی از رشد و دگرگونیِ انسان هستد. پایان نامه ی حاضر، با تمرکز بر روی مراحل سیر شعری ریچ از تغییری در دنیا به عکس هایی فوری از یک عروس، سپس به شیرجه به درون کشتی شکسته و در نهایت به صبری عجیب مرا تا اینجا آورده، به بررسی این مراحل در قالب نظر شوالتر در رابطه با سه مرحله ی پیشرفت ادبی زنان یعنی مرحله ی زنانه، زن گرا و زن محور می پ...
15 صفحه اولValproic acid producing a Reye-like syndrome.
.Although several cases of acute hepatic failure associated with the administration of valproic acid (VPA) have been reported, the pathogenesis of this problem remains unclear. We report the case of a 40 month old male with a chronic seizure disorder treated with VPA and phenytoin for two years, who developed sudden progressive neurological deterioration with evidence of increased intracranial ...
متن کاملCT findings in adult Reye syndrome.
Reye syndrome, a condition of unknown etiology, is characterized by encephalopathy and fatty infiltration of the liver after viral infections, notably influenza B and varicella [1] . A history of relatively large doses of aspirin ingested during the infection is usually elicited [2] . Reye syndrome is seen most often in children ages 6 months to 15 years; the computed tomographic (CT) findings ...
متن کاملPartial trisomy 13 with features similar to C syndrome.
We report a case of partial trisomy 13 with trigonocephaly, upslant eyes, long smooth philtrum, polydactyly, agenesis of right kidney and mild developmental delay. In this family phenotypically normal mother had pericentric inversion of chromosome 13 and the child (proband) received recombinant 13 from the mother. Genetic counselling of the family for reproductive risks and testing siblings of ...
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ژورنال
عنوان ژورنال: Proceedings of the National Academy of Sciences
سال: 1984
ISSN: 0027-8424,1091-6490
DOI: 10.1073/pnas.81.19.6169