Results 11 to 20 of about 2,184 (211)
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
doaj +3 more sources
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
doaj +2 more sources
Reye syndrome and liver transplantation [PDF]
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
doaj +1 more source
Griscelli syndrome: A case report of Reye′s syndrome and atopic dermatitis history [PDF]
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
doaj +1 more source
Neurologic Clinics, 1985 Reye syndrome has emerged as the quintessential example of an acute metabolic encephalopathy. The clinical presentation is quite stereotyped in most instances permitting rapid, accurate diagnosis and early therapeutic intervention. Intoxications and certain inborn metabolic errors may mimic Reye syndrome. All patients with a recurrent episode should be
Darryl C. De Vivo
openaire +3 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
wiley +1 more source
What are the clues for an inherited metabolic disorder in Reye syndrome? A single Centre study of 58 children [PDF]
, 2022 International audienceObjectivesReye Syndrome is an acute encephalopathy with increased liver enzymes and blood ammonia, without jaundice. The prevalence of an underlying inherited metabolic disorder (IMD) is unclear, nor the clinical or biological ...
Violette Goetz +29 more
core +1 more source
, 2022 Tato bakalářská práce popisuje vzácné onemocnění zvané Reyův syndrom. Začátek práce pojednává o historii a četnosti výskytu onemocnění. Samostatná kapitola je věnována kyselině acetylsalicylové, která k tomuto onemocnění bezprostředně patří.
Konečná, Veronika
core
Reye Syndrome Associated with Vaccination with Live Virus Vaccines [PDF]
, 1979 To determine whether vaccination with live virus vaccines may be etiologi cally related to Reye syndrome, we examined 404 cases reported to the Center for Disease Control.
Schonberger, Lawrence +7 more
core +1 more source