Works matching IS 20358377 AND DT 2022 AND VI 14 AND IP 2


Results: 19
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    Italian Case Report with a Double Mutation in PSEN1 (K311R and E318G).

    Published in:
    Neurology International, 2022, v. 14, n. 2, p. 417, doi. 10.3390/neurolint14020034
    By:
    • Bisceglia, Paola;
    • Lo Vecchio, Filomena;
    • Latino, Raffaela Rita;
    • Gravina, Carolina;
    • Urbano, Maria;
    • la Torre, Annamaria;
    • Desina, Gaetano;
    • Greco, Antonio;
    • Leone, Maurizio;
    • Antonioni, Annibale
    Publication type:
    Article
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    Volume of Amygdala Subregions and Plasma Levels of Brain-Derived Neurotrophic Factor and Cortisol in Patients with s/s Genotype of Serotonin Transporter Gene Polymorphism of First-Episode and Drug-Naive Major Depressive Disorder: An Exploratory Study.

    Published in:
    Neurology International, 2022, v. 14, n. 2, p. 378, doi. 10.3390/neurolint14020031
    By:
    • Okamoto, Naomichi;
    • Watanabe, Keita;
    • Tesen, Hirofumi;
    • Ikenouchi, Atsuko;
    • Igata, Ryohei;
    • Konishi, Yuki;
    • Natsuyama, Tomoya;
    • Fujii, Rintaro;
    • Kakeda, Shingo;
    • Kishi, Taro;
    • Iwata, Nakao;
    • Yoshimura, Reiji
    Publication type:
    Article
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    Advances in Neurodegenerative Diseases.

    Published in:
    Neurology International, 2022, v. 14, n. 2, p. 336, doi. 10.3390/neurolint14020027
    By:
    • Siokas, Vasileios;
    • Dardiotis, Efthimios
    Publication type:
    Article
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