Works matching IS 2328-9503 AND VI 1 AND IP 12 AND DT 2014


Results: 11
    1
    2
    3
    4
    5

    Mutations in PTRH2 cause novel infantile-onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weakness.

    Published in:
    Annals of Clinical & Translational Neurology, 2014, v. 1, n. 12, p. 1024, doi. 10.1002/acn3.149
    By:
    • Hu, Hao;
    • Matter, Michelle L.;
    • Issa‐Jahns, Lina;
    • Jijiwa, Mayumi;
    • Kraemer, Nadine;
    • Musante, Luciana;
    • Vega, Michelle;
    • Ninnemann, Olaf;
    • Schindler, Detlev;
    • Damatova, Natalia;
    • Eirich, Katharina;
    • Sifringer, Marco;
    • Schrötter, Sandra;
    • Eickholt, Britta J.;
    • Heuvel, Lambert;
    • Casamina, Chanel;
    • Stoltenburg‐Didinger, Gisela;
    • Ropers, Hans‐Hilger;
    • Wienker, Thomas F.;
    • Hübner, Christoph
    Publication type:
    Article
    6
    7
    8

    Sirtuin 1 activator SRT2104 protects Huntington's disease mice.

    Published in:
    Annals of Clinical & Translational Neurology, 2014, v. 1, n. 12, p. 1047, doi. 10.1002/acn3.135
    By:
    • Jiang, Mali;
    • Zheng, Jennifer;
    • Peng, Qi;
    • Hou, Zhipeng;
    • Zhang, Jiangyang;
    • Mori, Susumu;
    • Ellis, James L.;
    • Vlasuk, George P.;
    • Fries, Harvey;
    • Suri, Vipin;
    • Duan, Wenzhen
    Publication type:
    Article
    9
    10
    11

    Issue Information.

    Published in:
    Annals of Clinical & Translational Neurology, 2014, v. 1, n. 12, p. i, doi. 10.1002/acn3.15
    Publication type:
    Article