Search Results - "Perillat, Lucie"

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  1. 1

    Generation and characterization of a novel mouse model of Becker Muscular Dystrophy with a deletion of exons 52 to 55 by Perillat, Lucie O M, Wong, Tatianna W Y, Maino, Eleonora, Ahmed, Abdalla, Scott, Ori, Hyatt, Elzbieta, Delgado-Olguin, Paul, Visuvanathan, Shagana, Ivakine, Evgueni A, Cohn, Ronald D

    Published in Disease models & mechanisms (05-08-2024)
    “…Becker Muscular Dystrophy (BMD) is a rare X-linked recessive neuromuscular disorder frequently caused by in-frame deletions in the DMD gene that result in the…”
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    Journal Article
  2. 2

    Clinical recommendations: The role of mechanisms in the GRADE framework by Perillat, Lucie, Mercuri, Mathew

    “…The Grading of Recommendations Assessment, Development and Evaluation (GRADE) framework has become one of the most influential frameworks for assessing quality…”
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  3. 3

    COVID‐19 and the generation of novel scientific knowledge: Evidence‐based decisions and data sharing by Perillat, Lucie, Baigrie, Brian S.

    Published in Journal of evaluation in clinical practice (01-06-2021)
    “…Rationale, aims and objectives The COVID‐19 pandemic has impacted every facet of society, including medical research. This paper is the second part of a series…”
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    Journal Article
  4. 4

    COVID‐19 and the generation of novel scientific knowledge: Research questions and study designs by Perillat, Lucie, Baigrie, Brian S.

    Published in Journal of evaluation in clinical practice (01-06-2021)
    “…Rationale, aims, and objectives One of the sectors challenged by the COVID‐19 pandemic is medical research. COVID‐19 originates from a novel coronavirus…”
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    Journal Article
  5. 5

    Advances in CRISPR/Cas9 Genome Editing for the Treatment of Muscular Dystrophies by Fatehi, Sina, Marks, Ryan M, Rok, Matthew J, Perillat, Lucie, Ivakine, Evgueni A, Cohn, Ronald D

    Published in Human gene therapy (01-05-2023)
    “…Muscular dystrophies (MDs) comprise a diverse group of inherited disorders characterized by progressive muscle loss and weakness. Given the genetic etiology…”
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    Journal Article