Results 11 to 20 of about 1,147,373 (216)
Pediatric Neurology Briefs, 1987 Twenty-six cases of Reye syndrome occurring between 1973 and 1982 have been reviewed in relation to aspirin ingestion at the Children’s Hospital, Camperdown, Australia (formerly the Royal Alexandra Hospital for Children in Sydney), where Reye first ...
J Gordon Millichap
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Potential alternatives in treatment of kawasaki disease to reduce the extremely rare risk of reye syndrome [PDF]
Frontiers in PediatricsBackground/objective: Kawasaki disease is an acute, systemic vasculitis most commonly observed in young Asian children. While the exact pathogenesis remains unknown, it is thought to be triggered by a pathogenic exposure that elicits an inflammatory ...
Ethan J. Johnson +5 more
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Reye Syndrome and Anti-Emetics
Pediatric Neurology Briefs, 1991 A drug-induced encephalopathy mainly by anti-emetics in two children with a diagnosis of Reye syndrome is reported from the Department of Paediatrics, University Hospital, Gasthuisberg, Leuven, Belgium.
J Gordon Millichap
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REYE-LIKE SYNDROME IN THREE-YEAR-OLD CHILD [PDF]
Безопасность и риск фармакотерапии, 2018 The article reviews the literature on classical and atypical Reye’s syndrome, explores the circumstances that contribute to its occurrence, provides criteria for diagnosing with an illustration in the form of an authentic case of Reye-like disease in a ...
S. S. Postnikov +5 more
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Reye syndrome and liver transplantation
The Turkish Journal of Pediatrics, 2010 Reye syndrome is a rare, but severe and often fatal disease. The etiology of the classical Reye syndrome is unknown, but it is typically preceded by a viral infection with a free interval of three to five days.
Murat Cağ +4 more
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Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism [PDF]
BMC Pediatrics, 2002 Background Hyperammonemia, hypoglycemia, hepatopathy, and ventricular tachycardia are common presenting features of carnitine-acylcarnitine translocase deficiency (Mendelian Inheritance in Man database: *212138), a mitochondrial fatty acid oxidation ...
Armstrong Dawna L +5 more
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Griscelli syndrome: A case report of Reye′s syndrome and atopic dermatitis history
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2008 Griscelli syndrome (GS) is a rare autosomal recessive disorder that results in pigmentary dilution of the skin and the hair (silver hair), with the presence of large clumps of pigment in hair shafts, and an accumulation of melanosomes in melanocytes ...
Kirzioglu Z, Altun A
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Trends in Neurosciences, 1982 Reye's syndrome (encephalopathy with fatty infiltration of the viscera) is an acute illness of childhood that produces hepatic dysfunction and metabolic encephalopathy. The disease is fatal in as many as 40% of cases. The cause is unknown. Several environmental agents, particularly salicylates and aflatoxin, have been implicated as possible toxins in ...
D A, Richmond, T, Stair
+8 more sources
Hepatology, EarlyView., 2022 A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan +19 more
wiley +1 more source
AASLD practice guidance on drug, herbal, and dietary supplement–induced liver injury
, 2022 Hepatology, EarlyView.
Robert J. Fontana +6 more
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