Results 31 to 40 of about 2,184 (211)
Carnitine Deficiency Syndromes
Pediatric Neurology Briefs, 1990 Carnitine deficiency syndromes manifested as metabolic encephalopathy, lipid storage myopathy, or cardiomyopathy are reviewed from the Department of Pediatrics, Park Nicollet Medical Center, Minneapolis, MN.
J Gordon Millichap
doaj +1 more source
Aspirin as a Risk Factor in Reye\u27s Syndrome [PDF]
, 1982 Fifty-six cases of Reye\u27s syndrome (RS) in school-aged children were reported in Michigan during the winter of 1979-1980. The parents of 25 of these children were interviewed in the spring of 1980, as were controls matched to the cases for age, race ...
Hall, William N. +3 more
core +1 more source
Cells, 2018 Mitochondrial fatty acid β-oxidation (FAO) is the primary pathway for fatty acid metabolism in humans, performing a key role in liver, heart and skeletal muscle energy homeostasis.
Alice J. Sharpe, Matthew McKenzie
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Defining and Measuring Developmental Regression During Childhood: A Scoping Review
Autism Research, EarlyView.ABSTRACT Developmental regression during childhood is inconsistently defined and measured, resulting in delayed diagnostic discovery and intervention. This study aimed to examine published definitions and measures for developmental regression. A comprehensive search strategy was applied to Medline, Embase, Cochrane, and PsycINFO databases.
Kirsten Furley +4 more
wiley +1 more source
Is Reye’s syndrome still a valid diagnosis? [PDF]
, 2014 Reye’s syndrome is characterised by acute non-inflammatory encephalopathy and fatty degeneration of the liver. The exact aetiology of the syndrome is unknown, but there is an association with viral infections and the use of aspirin.
Du Toit-Prinsloo, Lorraine +2 more
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Adult Reye-like syndrome associated with serologic evidence of acute parvovirus B19 infection
Brazilian Journal of Infectious Diseases, 2011 Reye's syndrome is an infrequently diagnosed medical condition affecting mainly children. The etiology, epidemiology and natural history of Reye's syndrome have been cloudily written in footnotes of medical books and exotic papers since the initial ...
Paulo Sérgio Gonçalves da Costa, PhD +4 more
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Organelle‐Resolved Tetrazine‐trans‐Cyclooctene Click Chemistry for Cargo Delivery and Release
Chemistry – A European Journal, EarlyView.Bioorthogonal click chemistry tools provide a means for specific intracellular conjugation of molecules. In this study, we used reactive tetrazine (Tz) and TCO moieties for labeling of organelles and organelle‐specific delivery and activation of doxorubicin prodrugs.
Oleh Durydivka +6 more
wiley +1 more source
Liver Ultrastructure in Mitochondrial Urea Cycle Enzyme Deficiencies and Comparison with Reye\u27s Syndrome [PDF]
, 1984 The liver ultrastructural findings in two girls with partial carbamyl phosphate synthetase I (CPS) deficiency and their heterozygote parents and two siblings with ornithine transcarbamylase (OTC) deficiency are described. Liver ultrastructure in the four
Mcreynolds, John W. +3 more
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Italian Journal of Pediatrics, 2012 Medium chain acyl CoA dehydrogenase deficiency (MCAD) is the most common inborn error of fatty acid oxidation. This condition may lead to cellular energy shortage and cause severe clinical events such as hypoketotic hypoglycemia, Reye syndrome and sudden
Lovera Cristina +8 more
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A long-term follow-up of cognitive, emotional, and behavioural sequelae to Reye syndrome [PDF]
, 1999 Eighteen adolescents who had survived Reye syndrome (RS) in early childhood were assessed on cognitive, emotional, and behavioural variables in a second follow-up study tracking this group. Siblings were used as controls.
Glasgow, J F T +8 more
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