Results 171 to 180 of about 2,184 (211)
Some of the next articles are maybe not open access.
Archives of Pediatrics & Adolescent Medicine, 1978
The clinical diagnosis of recurrent Reye's syndrome can be made only after a systemic exclusion of other diagnostic possibilities. We report such a case, providing guidelines for a complete clinical and biochenical evaluation of this entity. If a comprehensive study of patients experiencing recurrent Reye's syndrome is to be made, each patient must be ...
M E, Pichichero, E R, McCabe
openaire +2 more sources
The clinical diagnosis of recurrent Reye's syndrome can be made only after a systemic exclusion of other diagnostic possibilities. We report such a case, providing guidelines for a complete clinical and biochenical evaluation of this entity. If a comprehensive study of patients experiencing recurrent Reye's syndrome is to be made, each patient must be ...
M E, Pichichero, E R, McCabe
openaire +2 more sources
Pancreatitis and Reye's Syndrome
Archives of Pediatrics & Adolescent Medicine, 1979A review of 18 cases of Reye's syndrome autopsied at Indiana University Hospital since 1970 was done to document pancreatic lesions associated with the syndrome. A spectrum of inflammatory lesions was identified and grouped into four categories: group 1, no changes; group 2, minimal microscopic changes; group 3, moderate changes, ie, focal necrosis ...
G H, Ellis, L D, Mirkin, M C, Mills
openaire +2 more sources
Salicylate and Reye's Syndrome
Pediatrics, 1981Starko et at1 have written an interesting paper, their observations concerning the interaction of fever, viral illness, and salicylates in the pathogenesis of Reye's syndrome appear plausible. However, their data do not unequivocally support their conclusion "salicylate causes Reye's syndrome." Although the authors are investigating the ...
openaire +2 more sources
The Indian Journal of Pediatrics, 1981
Reye’s syndrome was diagnosed in about 15% of cases of encephalopathy syndrome admitted in hospital. Hypoglycemia, considered a hallmark of the disease, was an uncommon observation particularly in patients beyond one year of age (8.5%). Transaminases were more useful than hypoglycemia for suspecting this syndrome (raised in 80% of cases).
V, Kalra, H P, Sachdev, P S, Menon
openaire +2 more sources
Reye’s syndrome was diagnosed in about 15% of cases of encephalopathy syndrome admitted in hospital. Hypoglycemia, considered a hallmark of the disease, was an uncommon observation particularly in patients beyond one year of age (8.5%). Transaminases were more useful than hypoglycemia for suspecting this syndrome (raised in 80% of cases).
V, Kalra, H P, Sachdev, P S, Menon
openaire +2 more sources
Irish Journal of Medical Science, 1982
Early recognition of Reye’s syndrome is important as prompt treatment may reduce morbidity and mortality. We report a case where the syndrome presented as ketoacidosis in a known diabetic.
M, McEvoy, M I, Drury
openaire +2 more sources
Early recognition of Reye’s syndrome is important as prompt treatment may reduce morbidity and mortality. We report a case where the syndrome presented as ketoacidosis in a known diabetic.
M, McEvoy, M I, Drury
openaire +2 more sources
[Reye syndrome and Reye-like syndrome].
Nihon rinsho. Japanese journal of clinical medicine, 2011Reye syndrome (RS) is an acute metabolic encephalopathy and hepatopathy affecting children and adolescents. Outbreaks of RS were common in United States until the early 1980s. However, after the abolition of salicylate (aspirin) therapy for infectious diseases such as influenza or varicella in patients under 18 years of age the incidence decreased. Now
openaire +1 more source
Archives of Pediatrics & Adolescent Medicine, 1973
To the Editor. —The report by Glasgow et al 1 on the occurrence of Reye syndrome in the absence of severe fatty infiltration of the liver represents both some useful clinical observation and a disservice to the effort to define Reye syndrome more precisely. The latter objection arises, in part, from a most dubious clinical example (case 1).
openaire +2 more sources
To the Editor. —The report by Glasgow et al 1 on the occurrence of Reye syndrome in the absence of severe fatty infiltration of the liver represents both some useful clinical observation and a disservice to the effort to define Reye syndrome more precisely. The latter objection arises, in part, from a most dubious clinical example (case 1).
openaire +2 more sources
Salicylates and Reye's Syndrome
JAMA: The Journal of the American Medical Association, 1983To the Editor.— Daniels et al (1983; 249:1311), in their discussion of salicylate use and Reye's syndrome, seem to use the terms aspirin and salicylates almost interchangeably. If we are to lessen the "scientific uncertainties" connected with the studies of salicylate use and Reye's syndrome, may I suggest that we first make a clear statement about ...
openaire +2 more sources