Works matching AU Argyriou, Catherine


Results: 5
    1

    Peroxisomes : novel findings and future directions.

    Published in:
    Histochemistry & Cell Biology, 2023, v. 159, n. 5, p. 379, doi. 10.1007/s00418-023-02201-9
    By:
    • Pedrosa, Ana G.;
    • Reglinski, Katharina;
    • Lismont, Celien;
    • Kors, Suzan;
    • Costello, Joseph;
    • Rodrigues, Tony A.;
    • Marques, Mariana;
    • Linka, Nicole;
    • Argyriou, Catherine;
    • Weinhofer, Isabelle;
    • Kocherlakota, Sai;
    • Riccio, Victoria;
    • Ferreira, Vanessa;
    • Di Cara, Francesca;
    • Ferreira, Ana Rita;
    • Francisco, Tânia;
    • Azevedo, Jorge E.;
    • Ribeiro, Daniela
    Publication type:
    Article
    2

    Clinical, neuroradiological, and molecular characterization of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations: a case series.

    Published in:
    Neurogenetics, 2022, v. 23, n. 2, p. 115, doi. 10.1007/s10048-022-00684-7
    By:
    • Cheung, Anthony;
    • Argyriou, Catherine;
    • Yergeau, Christine;
    • D'Souza, Yasmin;
    • Riou, Émilie;
    • Lévesque, Sébastien;
    • Raymond, Gerald;
    • Daba, Mebratu;
    • Rtskhiladze, Irakli;
    • Tkemaladze, Tinatin;
    • Adang, Laura;
    • La Piana, Roberta;
    • Bernard, Geneviève;
    • Braverman, Nancy
    Publication type:
    Article
    3
    4
    5

    The biochemical basis of mitochondrial dysfunction in Zellweger Spectrum Disorder.

    Published in:
    EMBO Reports, 2021, v. 22, n. 10, p. 1, doi. 10.15252/embr.202051991
    By:
    • Nuebel, Esther;
    • Morgan, Jeffrey T;
    • Fogarty, Sarah;
    • Winter, Jacob M;
    • Lettlova, Sandra;
    • Berg, Jordan A;
    • Chen, Yu‐Chan;
    • Kidwell, Chelsea U;
    • Maschek, J Alan;
    • Clowers, Katie J;
    • Argyriou, Catherine;
    • Chen, Lingxiao;
    • Wittig, Ilka;
    • Cox, James E;
    • Roh‐Johnson, Minna;
    • Braverman, Nancy;
    • Bonkowsky, Joshua;
    • Gygi, Steven P;
    • Rutter, Jared
    Publication type:
    Article