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Effets secondaires graves: Le médicament contre la SEP Daclizumab (Zinbryta) a été retiré du marché mondial

04 mars 2018 – Le daclizumab (Zinbryta) a été approuvé pour le traitement de la sclérose en plaques (SEP) rémittente cyclique en mai 2016 aux États-Unis, en juillet 2016 dans l’Union européenne (UE) et en janvier 2017 en Suisse.

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Myopathie nécrosante immuno-médiée associée aux statines

Ce sont des informations de Swissmedic à l’adresse www.swissmedicinfo.ch.

Au cours des dernières années, les statines (inhibiteurs de la HMG-CoA réductase) ont été identifiées comme étant un des facteurs déclencheurs possibles d’une maladie rare: la myopathie nécrosante immuno-médiée (Immune-mediated necrotising myopathy,

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  • New candidate cancer genes identified using math models novembre 15, 2019
    Computational modeling is the use of computers to simulate and study the behavior of complex systems. Computational approaches are widely adopted in the bioimedical sciences and can be used to sift through large volumes of complex data to extract recurrent patterns that may point to a disease's causes and effects.
  • Turning 'junk' DNA into gold novembre 15, 2019
    Mining the rich uncharted territory of the genome or genetic material of a cancer cell has yielded gold for Princess Margaret scientists: new protein targets for drug development against prostate cancer.
  • Researchers take first step toward genetic test for childhood short-sightedness novembre 15, 2019
    Researchers from the Universities of Cardiff and Bristol have devised a test that could in future help to identify children at risk of developing a very common eye condition.
  • Researchers link sisters' paralysis to an 'extremely rare' genetic variant novembre 15, 2019
    Following a nearly 25-year search across three continents, parents of a pair of sisters—who as children slowly became paralyzed from the waist down—finally have a diagnosis, according to researchers at University of Southern California (USC) and Translational Genomics Research Institute (TGen), an affiliate of City of Hope.
  • Genetic variation in individual brain cell types may predict disease risk novembre 15, 2019
    One might think that the primary cause of most genetically linked diseases comes from mutations in coding DNA—alterations in coding regions of the genome that can lead directly to changes in the expression of particular proteins important for a healthy body. But the majority of human DNA is non-coding DNA—regions of DNA that do not […]
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