Torthaí cuardaigh - Bright, Alicia

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  1. 1
    Reply to du Moulin et al.: Cerebral vasculopathy is a common hallmark in individuals with SAMHD1 mutations

    Reply to du Moulin et al.: Cerebral vasculopathy is a common hallmark in individuals with SAMHD1 mutations de réir Xin, Baozhong, Li, Wei, Bright, Alicia, Hinze, Claas, Wang, Heng

    Foilsithe / Cruthaithe 2011
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  2. 2
    Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke

    Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke de réir Xin, Baozhong, Jones, Stephen, Puffenberger, Erik G., Hinze, Claas, Bright, Alicia, Tan, Haiyan, Zhou, Aimin, Wu, Guiyun, Vargus-Adams, Jilda, Agamanolis, Dimitris, Wang, Heng

    Foilsithe / Cruthaithe 2011
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  3. 3
    Oral Ganglioside Supplement Improves Growth and Development in Patients with Ganglioside GM3 Synthase Deficiency

    Oral Ganglioside Supplement Improves Growth and Development in Patients with Ganglioside GM3 Synthase Deficiency de réir Wang, Heng, Sency, Valerie, McJarrow, Paul, Bright, Alicia, Huang, Qianyang, Cechner, Karen, Szekely, Julia, Brace, JoAnn, Wang, Andi, Liu, Danting, Rowan, Angela, Wiznitzer, Max, Zhou, Aimin, Xin, Baozhong

    Foilsithe / Cruthaithe 2018
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