Peter Baxter
Sheffield Children's NHS Foundation Trust(GB)Sheffield Children's Hospital(GB)
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Cerebral Palsy and Movement Disorders, Neonatal and fetal brain pathology, Epilepsy research and treatment, Infant Development and Preterm Care
Most-Cited Works
- → Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection(2006)670 cited
- → Mutations in antiquitin in individuals with pyridoxine-dependent seizures(2006)545 cited
- → Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome(2007)445 cited
- → Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus(2012)286 cited
- → Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)(2010)264 cited
- → Long-term benefits and adverse effects of intermittent versus daily glucocorticoids in boys with Duchenne muscular dystrophy(2012)256 cited