Eija Anttila

Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy

Christine P. Diggle, Stacey J. Sukoff Rizzo, Michael Popiolek et al. · The American Journal of Human Genetics · 2016 · 80 citations · Full text

Biallelic Mutations, Neurological Disorder, Striatal Pde10a +10

Neurally adjusted ventilatory assist (NAVA) in pediatric intensive care—A randomized controlled trial

Merja Kallio, Outi Peltoniemi, Eija Anttila et al. · Pediatric Pulmonology · 2014 · 62 citations

Marked variation in oxycodone pharmacokinetics in infants

Marja‐Leena Pokela, Eija Anttila, Timo Seppαlä et al. · Pediatric Anesthesia · 2005 · 54 citations

Early hypoadrenalism in premature infants at risk for bronchopulmonary dysplasia or death

Päivi Nykänen, Eija Anttila, Kirsti Heinonen et al. · Acta Paediatrica · 2007 · 30 citations

Electrical activity of the diaphragm during neurally adjusted ventilatory assist in pediatric patients

Merja Kallio, Outi Peltoniemi, Eija Anttila et al. · Pediatric Pulmonology · 2014 · 19 citations