Results 161 to 170 of about 49,127 (197)

Biochemical Relationships Between Reye’s and Reye’s-Like Metabolic and Toxicological Syndromes

Medical Toxicology and Adverse Drug Experience, 1989
Reye's syndrome is a hepatic encephalopathy with fatty infiltration of the liver and is due to mitochondrial dysfunction. Knowledge of the mechanisms causing Reye's syndrome has been gained from the study of Reye's syndrome-like diseases, including inborn errors of mitochondrial energy production, viral disease and toxicological injury.
J, Osterloh, W, Cunningham, A, Dixon, D, Combest   +3 more
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Metabolic cause of Reye-like syndrome.

Bratislavske lekarske listy, 2002
The most frequent metabolic cause of Reye-like syndrome is medium chain acyl-CoA dehydrogenase (MCAD) deficiency. The authors describe a gypsy boy who was repeatedly hospitalised due to symptoms of Reye-like syndrome (serious hypoglycemia, loss of consciousness, seizures, increased values of aminotransferases, decreased values of free carnitine).
Bzduch, Vladimir, Behulova, Darina, Lehnert, Willy, Fabriciová, K., Kozak, L., Salingova, A., Hrabincová, E., Benedeková, Marta   +7 more
openaire   +1 more source

Recurrent, familial Reye-like syndrome with a new complex amino and organic aciduria

European Journal of Pediatrics, 1990
Five of 13 siblings from a Jewish-Ashkenazi family suffered from recurrent Reye-like episodes. During attacks, these patients excreted alpha-keto-adipic, alpha-hydroxy-adipic, and alpha-aminoadipic acids, branched-chain keto acids and saccharopine in addition to lactic, pyruvic, and dicarboxylic acids characteristic of Reye syndrome.
O N, Elpeleg, E, Christensen, H, Hurvitz, D, Branski   +3 more
openaire   +2 more sources

[Reye syndrome and Reye-like syndrome].

Nihon rinsho. Japanese journal of clinical medicine, 2011
Reye 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
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Involvement of Carnitine in Reye’s and Reye-Like Syndromes

1997
In 1963 Reye and colleagues described a new clinical pathological entity in childhood, called Reye’s syndrome (RS),1 characterized by non-inflammatory encephalopathy and fatty degeneration of the viscera. RS is a rare, acute, and often fatal metabolic disease affecting mostly 7- to 9-year old children after a few days of mild viral infection, treated ...
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[Description of a case of Reye's-like syndrome with fatal outcome].

Minerva anestesiologica, 1998
A Reye Like Syndrome case occurred in a twelve year-old little girl with a previous familiar history is reported. The little patient was admitted in the pediatric ward for fever, vomiting and aspecific respiratory symptoms and developed very quickly a severe metabolic acidosis, alterations of consciousness, hypoxia, tissular hypoperfusion, multiple ...
R, Oggioni, R, Iamello, G, Tulli
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[Reye-like syndrome following valproate therapy in an adult].

Psychiatrie, Neurologie, und medizinische Psychologie, 1989
Three months after anticonvulsive regulation by means of the spasmolytic agent Convulsofin, a 46-year-old man suffered severe hepatosis, and when the preparation was discontinued he suffered a severe cerebral dysfunction. The clinical picture is interpreted as being "similar to the Reye syndrome", and distinctions between this and previously reported ...
M, Klein, U, Wendt
openaire   +1 more source

Familial Reye-Like Syndrome: A Presentation of Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency

Pediatrics, 1987
A 20-month-old girl with a family history of two siblings who died of an encephalopathy diagnosed as Reye syndrome presented to an emergency room in hypoglycemic coma and was found to have medium-chain acyl-coenzyme A dehydrogenase deficiency. The salient clinical and biochemical features of this newly described inborn error of fatty acid metabolism ...
B, Taubman, D E, Hale, R I, Kelley
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Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemia

European Journal of Pediatrics, 1993
An apparently healthy girl aged 2 years 9 months developed a coma with hepatomegaly within 24 h after an influenza-like infection. Plasma glucose and urinary organic acid profile were normal but plasma and urinary carnitine concentrations were increased. Despite symptomatic therapy, she died 11 days later.
C, Vianey-Saban, B, Mousson, C, Bertrand, D, Stamm, R, Dumoulin, M T, Zabot, P, Divry, D, Floret, M, Mathieu   +8 more
openaire   +2 more sources

Mass spectrometric identification of abnormal aromatic compounds in the urine of a child with Reye's like syndrome

Biological Mass Spectrometry, 1984
The urine of a young child with hypoglycemia and a Reye's like syndrome contained an excess of unusual aromatic products with a three carbon chain, phenylpropionylglycine and 3- and 4-(hydroxyphenyl)propionic and 3-(3-methoxy-4-hydroxyphenyl)propionic acids, as well as of organic acids usually found in fatty acid beta-oxidation defects: the mono- and ...
F, Rocchiccioli, P H, Cartier, P F, Bougnères   +2 more
openaire   +2 more sources