Lyvia Dabydeen

Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>

Yanick J. Crow, Diana Chase, Johanna L. Schmidt et al. · American Journal of Medical Genetics Part A · 2015 · 589 citations · Full text

Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study

Gillian Rice, Gabriella Forte, Marcin Szynkiewicz et al. · The Lancet Neurology · 2013 · 425 citations · Full text

Genetic Disorder, Aicardi-goutières Syndrome, Genetics +9

Is hemiplegic cerebral palsy equivalent to amblyopia of the corticospinal system?

J A Eyre, Martin Smith, Lyvia Dabydeen et al. · Annals of Neurology · 2007 · 265 citations

Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial

Finbar O’Callaghan, Stuart W. Edwards, Fabienne Dietrich Alber et al. · The Lancet Child & Adolescent Health · 2018 · 161 citations · Full text

Pain Disorders, Hormonal Treatment, Pediatrics +6

Symptoms of depression, anxiety, and stress in parents of young children with epilepsy: A case controlled population-based study

Colin Reilly, Patricia Atkinson, Ayesha Memon et al. · Epilepsy & Behavior · 2018 · 94 citations · Full text

Child Psychology, Population-based Study, Psychiatry +11