نتایج جستجو برای: reye

تعداد نتایج: 271  

2012
Marga Sturm Diran Herebian Martina Mueller Maurice D. Laryea Ute Spiekerkoetter

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency (OMIM 201450) is the most common inherited disorder of fatty acid metabolism presenting with hypoglycaemia, hepatopathy and Reye-like symptoms during catabolism. In the past, the majority of patients carried the prevalent c.985A>G mutation in the ACADM gene. Since the introduction of newborn screening many other mutations with unknown clinic...

Journal: :Archives of disease in childhood 1981
S Ozsoylu

Three children with Reye's syndrome are described. One child died, the second had mild and transient illness, and the third had recurrent episodes. In all 3 children a muscle biopsy showed pronounced infiltration of the myofibres with fat microdroplets as shown by the oil red O stain and by electron microscopical examination. We suggest that needle biopsy of muscle may be a quick and safe aid t...

2017

This is a rare syndrome, characterised by an acute, life-threatening, non-inflammatory encephalopathy and fatty degeneration of the liver with minimal or no clinical signs of liver involvement. In classic Reye's syndrome, there is a severe but self-limiting disturbance of mitochondrial structure and associated enzymatic disturbances usually lasting about six days. This is accompanied by an inte...

Journal: :Scottish medical journal 1990
T C Smith

In 1986 there was a public warning in the United Kingdom about a link between the consumption of aspirin and Reye's syndrome. To find out if the use of aspirin and paracetamol in children had altered, and whether the incidence of Reye's syndrome had changed since a previous study, parents were interviewed in Belfast and London, and the British Reye's Syndrome Surveillance System data were revie...

2010
Marta Coll Chiara Piroddi Jeroen Steenbeek Kristin Kaschner Frida Ben Rais Lasram Jacopo Aguzzi Enric Ballesteros Carlo Nike Bianchi Jordi Corbera Thanos Dailianis Roberto Danovaro Marta Estrada Carlo Froglia Bella S. Galil Josep M. Gasol Ruthy Gertwagen João Gil François Guilhaumon Kathleen Kesner-Reyes Miltiadis-Spyridon Kitsos Athanasios Koukouras Nikolaos Lampadariou Elijah Laxamana Carlos M. López-Fé de la Cuadra Heike K. Lotze Daniel Martin David Mouillot Daniel Oro Saša Raicevich Josephine Rius-Barile Jose Ignacio Saiz-Salinas Carles San Vicente Samuel Somot José Templado Xavier Turon Dimitris Vafidis Roger Villanueva Eleni Voultsiadou

Marta Coll*, Chiara Piroddi, Jeroen Steenbeek, Kristin Kaschner, Frida Ben Rais Lasram, Jacopo Aguzzi, Enric Ballesteros, Carlo Nike Bianchi, Jordi Corbera, Thanos Dailianis, Roberto Danovaro, Marta Estrada, Carlo Froglia, Bella S. Galil, Josep M. Gasol, Ruthy Gertwagen, João Gil, François Guilhaumon, Kathleen Kesner-Reyes, Miltiadis-Spyridon Kitsos, Athanasios Koukouras, Nikolaos Lampadariou, ...

2006
Rodolfo Valdés Yenisley Medina William Ferro José A. Montero Tatiana Alvarez Déborah Geada Alberto Leyva Leonardo Gómez Sigifredo Padilla María del Carmen Abrahantes Rodolfo Valdes

Hepatitis B surface antigen immunopurification using a plant-derived specific antibody coupled to Sepharose CL-4B at different ligand densities Rodolfo Valdés, Yenisley Medina, William Ferro, José A. Montero, Tatiana Alvarez, Déborah Geada, Alberto Leyva, Leonardo Gómez, Sigifredo Padilla, Biunayki Reyes, Leonardo Pacín, Alejandro Figueroa, Andrés Tamayo, Lorely Milá, Yurisleydi Aldama and Marí...

2017

This is a rare syndrome, characterised by an acute, life-threatening, non-inflammatory encephalopathy and fatty degeneration of the liver with minimal or no clinical signs of liver involvement. In classic Reye's syndrome, there is a severe but self-limiting disturbance of mitochondrial structure and associated enzymatic disturbances usually lasting about six days. This is accompanied by an inte...

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