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  • Author Correction: BDNF Val66Met gene polymorphism modulates brain activity following rTMS-induced memory impairment.

    Published in:
    2022
    By:
    • Abellaneda‑Pérez, Kilian;
    • Martin‑Trias, Pablo;
    • Cassé‑Perrot, Catherine;
    • Vaqué‑Alcázar, Lídia;
    • Lanteaume, Laura;
    • Solana, Elisabeth;
    • Babiloni, Claudio;
    • Lizio, Roberta;
    • Junqué, Carme;
    • Bargalló, Núria;
    • Rossini, Paolo Maria;
    • Micallef, Joëlle;
    • Truillet, Romain;
    • Charles, Estelle;
    • Jouve, Elisabeth;
    • Bordet, Régis;
    • Santamaria, Joan;
    • Rossi, Simone;
    • Pascual‑Leone, Alvaro;
    • Blin, Olivier
    Publication type:
    Correction Notice

  • BDNF Val66Met gene polymorphism modulates brain activity following rTMS-induced memory impairment.

    Published in:
    Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-021-04175-x
    By:
    • Abellaneda-Pérez, Kilian;
    • Martin-Trias, Pablo;
    • Cassé-Perrot, Catherine;
    • Vaqué-Alcázar, Lídia;
    • Lanteaume, Laura;
    • Solana, Elisabeth;
    • Babiloni, Claudio;
    • Lizio, Roberta;
    • Junqué, Carme;
    • Bargalló, Núria;
    • Rossini, Paolo Maria;
    • Micallef, Joëlle;
    • Truillet, Romain;
    • Charles, Estelle;
    • Jouve, Elisabeth;
    • Bordet, Régis;
    • Santamaria, Joan;
    • Rossi, Simone;
    • Pascual-Leone, Alvaro;
    • Blin, Olivier
    Publication type:
    Article

  • Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study.

    Published in:
    Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-014-0218-1
    By:
    • Salort-Campana, Emmanuelle;
    • Nguyen, Karine;
    • Bernard, Rafaelle;
    • Jouve, Elisabeth;
    • Solé, Guilhem;
    • Nadaj-Pakleza, Aleksandra;
    • Niederhauser, Julien;
    • Charles, Estelle;
    • Ollagnon, Elisabeth;
    • Bouhour, Françoise;
    • Sacconi, Sabrina;
    • Echaniz-Laguna, Andoni;
    • Desnuelle, Claude;
    • Tranchant, Christine;
    • Vial, Christophe;
    • Magdinier, Frederique;
    • Bartoli, Marc;
    • Arne-Bes, Marie-Christine;
    • Ferrer, Xavier;
    • Kuntzer, Thierry
    Publication type:
    Article

  • Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study.

    Published in:
    Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 22, doi. 10.1186/s13023-014-0218-1
    By:
    • Salort-Campana, Emmanuelle;
    • Nguyen, Karine;
    • Bernard, Rafaelle;
    • Jouve, Elisabeth;
    • Solé, Guilhem;
    • Nadaj-Pakleza, Aleksandra;
    • Niederhauser, Julien;
    • Charles, Estelle;
    • Ollagnon, Elisabeth;
    • Bouhour, Françoise;
    • Sacconi, Sabrina;
    • Echaniz-Laguna, Andoni;
    • Desnuelle, Claude;
    • Tranchant, Christine;
    • Vial, Christophe;
    • Magdinier, Frederique;
    • Bartoli, Marc;
    • Arne-Bes, Marie-Christine;
    • Ferrer, Xavier;
    • Kuntzer, Thierry
    Publication type:
    Article