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2. Aicardi–Goutières syndrome harbours abundant systemic and brain-reactive autoantibodies. Issue 10 (6th June 2014)

4. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1. (16th January 2015)

6. Impact of COVID-19 lockdown in children with neurological disorders in Italy. Issue 2 (April 2021)

7. Neuroradiologic patterns and novel imaging findings in Aicardi-Goutières syndrome. (5th January 2016)

8. Patient‐reported outcomes measure for children born preterm: validation of the SOLE VLBWI Questionnaire, a new quality of life self‐assessment tool. (7th April 2016)

10. Synonymous Mutations in RNASEH2A Create Cryptic Splice Sites Impairing RNase H2 Enzyme Function in Aicardi–Goutières Syndrome. Issue 8 (13th May 2013)