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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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  • Study examines genetic testing in diverse young breast cancer patients over a decade janvier 28, 2020
    Breast cancer patients diagnosed under age 50 represent 18 percent of new invasive breast cancer cases in the United States. Compared to postmenopausal women, younger women are more likely to develop aggressive subtypes of breast cancer, have a worse prognosis with increased risk of recurrence, and have higher overall mortality. Young breast cancer patients also […]
  • Novel insight into chromosome 21 and its effect on Down syndrome janvier 28, 2020
    A UCL-led research team has, for the first time, identified specific regions of chromosome 21, which cause memory and decision-making problems in mice with Down syndrome, a finding that provides valuable new insight into the condition in humans.
  • Decoding sickle cell disease janvier 28, 2020
    When Lamarcus Jean visits the Hematology Clinic at Dana-Farber/Boston Children's Cancer and Blood Disorders Center, he makes himself right at home. The 6-year-old, whom his mom, Stephanie, describes as "wise beyond his years," has been a patient here since he was born.
  • Gender differences in autism janvier 28, 2020
    Tools used for screening autism may play a part in the failure to detect autism in girls and women, researchers at Bournemouth University have found.
  • New gene correction therapy for Duchenne muscular dystrophy janvier 28, 2020
    Duchenne type muscular dystrophy (DMD) is the most common hereditary muscular disease among children, leaving them wheelchair-bound before the age of 12 and reducing life expectancy. Researchers at Technical University of Munich (TUM), Ludwig Maximilian University of Munich (LMU) and the German Research Center for Environmental Health (Helmholtz Zentrum München) have developed a gene therapy […]
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