Results 31 to 40 of about 1,147,373 (216)
Isolation and Characterization of Novel Human Parechovirus from Clinical Samples
Emerging Infectious Diseases, 2007 Using Vero cells, we isolated a virus (NII561-2000) from a cerebrospinal fluid specimen of a 1-year-old girl with Reye syndrome. The determined amino acid sequence of the virus indicated that the isolate was a human parechovirus (HPeV), a member of ...
Kanako Watanabe +4 more
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Frontiers in Genetics, 2021 Inborn errors of mitochondrial fatty acid oxidation (FAO) comprise the most common group of disorders identified through expanded newborn screening mandated in all 50 states in the United States, affecting 1:10,000 newborns.
Evgenia Sklirou +8 more
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Nodal Enriques surfaces are Reye congruences [PDF]
, 2023 We show that every classical Enriques surface containing a smooth rational curve is a Reye congruence.Comment: 16 ...
Mezzedimi, Giacomo +2 more
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Reye syndrome and the value of electroencephalography in this syndrome [PDF]
, 1988 İç organların yağlı dejenerasyon ile birlikte olan bir ensefalopati olarak tanımlanan Reye sendromu, bir çocukluk çağı hastalığı olarak kabul edilir. Reye sendromunun ülkemizde daha önceleri inandığı kadar az olmadığı inancındayız.
core +1 more source
Non Salicylate-Associated Reye Syndrome: A Case Report
Acta Medica Iranica, 2019 Reye's syndrome (RS) is a rare disease, usually associated with consumption of salicylates during viral illness. In 1965, the first case of association between RS and salicylates was described in United Kingdom (UK).
Arsalan Azizi, Moslem Sedaghattalab
doaj +1 more source
Annals of Indian Academy of Neurology, 2018 Chickenpox (varicella) is primarily a disease of childhood which occurs due to infection with varicella-zoster virus (VZV). Primary VZV infection is rare in adults due to exposure in early childhood in our country.
Anuradha Mehta +4 more
doaj +1 more source
Revue Malienne d’Infectiologie et de Microbiologie, 2014 Objectif: Décrire les aspects épidémiologiques, cliniques et thérapeutiques des varicelles graves de l'adulte et de l'enfant. Méthode: Nous avons étudié prospectivement sur 5 ans, de février 2007 à Janvier 2012 l'ensemble des cas de varicelle grave admis
MI Wateba, S Saka, O Tidjani
doaj +3 more sources
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
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Arthroscopy, EarlyView.Abstract Patients with generalized ligamentous laxity undergoing hip arthroscopy have traditionally been challenging for hip arthroscopists when setting preoperative expectations. Recent literature confirms slower recovery, increased pain, and worse patient‐reported outcomes in the near postoperative period before ultimate normalization in the midterm,
Riley Hemstock, Moin Khan
wiley +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
doaj +1 more source