Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Reye like syndrome"'
Autor:
Mehmet Cihan Balci, Meryem Karaca, Arzu Selamioglu, Huseyin Kutay Korbeyli, Asli Durmus, Belkis Ak, Tugba Kozanoglu, Gulden Fatma Gokcay
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 38, Iss , Pp 101032- (2024)
Carnitine palmitoyltransferase I (CPT I) deficiency is an autosomal recessive disorder causing long-chain fatty acid oxidation defect, characterized by metabolic decompensation episodes accompanied by hypoketotic hypoglycemia, hepatomegaly, seizures,
Externí odkaz:
https://doaj.org/article/9db955c19bb542af9e6fa85dfd9a33c7
Akademický článek
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Autor:
S. S. Postnikov, S. V. Mikhailova, G. P. Bryusov, M. N. Kostyleva, A. N. Gratsianskaya, A. E. Ermilin
Publikováno v:
Безопасность и риск фармакотерапии, Vol 6, Iss 3, Pp 103-110 (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
Externí odkaz:
https://doaj.org/article/66a77ea126ea4e7e8309c26413d2f1ac
Autor:
Svetlana Viktorovna Lunenok, Tatyana Valerievna Piskareva, Anastasia Anatolievna Nemtseva, Yury Vasilievich Zobnin
Publikováno v:
Scientific medical Bulletin of Ugra. 25:35-43
The article presents the results of a commission and a comprehensive forensic medical examination on the “Criminal case on suspicion of S. of committing a crime under Part 1 of Art. 109 of the Criminal Code of the Russian Federation”, concerning
Publikováno v:
Muller Journal of Medical Sciences and Research, Vol 4, Iss 2, Pp 111-112 (2013)
Hepatic encephalopathy (HE) is an important and common metabolic disturbance in children. The causes are many. Reye-like syndrome (RLS) can manifest with hypoglycemia, hyperammonemia and altered sensorium with elevated liver enzymes as in Reye syndro
Externí odkaz:
https://doaj.org/article/4ad635dc16204423a47eb60962073378
Autor:
Sukru Arslan
Publikováno v:
Journal of Clinical and Analytical Medicine, Vol 5, Iss 93, Pp 191-194 (2013)
We performed a retrospective study to explore the mortality rates and prognosis of the Reye like syndrome in patients treated at Konya Research and Education Hospital. Twenty two children with ages between 5 months and 7 years old were included in th
Akademický článek
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Autor:
Armstrong Dawna L, Towbin Jeffrey A, Scheuerle Angela E, Scaglia Fernando, Sweetman Lawrence, Wong Lee-Jun C
Publikováno v:
BMC Pediatrics, Vol 2, Iss 1, p 12 (2002)
Abstract 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 o
Externí odkaz:
https://doaj.org/article/e3717fd3c34b4bdb95b2d8f4f220c604
Autor:
Kenichi Ikeda, Ken Sonoda
Publikováno v:
Kansenshogaku Zasshi. 83:658-660
We report a rare case of Reye's-like syndrome associated with suspected pertussis infection. A 26-year-old woman admitted comatose and found in laboratory studies to have acute liver dysfunction, severe hypoglycemia and prolonged prothrombin time, wa
Publikováno v:
Journal of medical primatology. 41(5)
Background A 15-year-old western lowland gorilla (Gorilla gorilla gorilla) died shortly after transfer to the North Carolina Zoo. Methods Complete blood count, serum biochemical analysis, and necropsy were performed. Results Combination of compatible