Interferon-related transcriptome alterations in the cerebrospinal fluid cells of Aicardi-Goutières patients.

@article{Izzotti2009InterferonrelatedTA,
  title={Interferon-related transcriptome alterations in the cerebrospinal fluid cells of Aicardi-Gouti{\`e}res patients.},
  author={Alberto Izzotti and Alessandra Pulliero and Simona Orcesi and Cristina Cartiglia and Maria Grazia Longobardi and Valeria Capra and Pierre Lebon and A Cama and Roberta La Piana and Giovanni Lanzi and Elisa Fazzi},
  journal={Brain pathology},
  year={2009},
  volume={19 4},
  pages={
          650-60
        }
}
Aicardi-Goutières syndrome (AGS) is a rare interferon (IFN)-related encephalopathy with onset during the first year of life. AGS, is clinically characterized by progressive microcephaly, bilateral basal ganglia calcification, cerebral atrophy, cerebrospinal fluid (CSF), lymphocytosis, delayed development of psychomotor abilities with pyramidal-extrapyramidal syndrome and mimics congenital viral infections. Microarray analysis examining the expression of 18 880 human genes has been applied to… CONTINUE READING
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