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Science (New York, N.Y.)|May 17, 2014
Mechanism of activation of protein kinase JAK2 by the growth hormone receptorAndrew J Brooks, Wei Dai, Megan L O'Mara, et al.
Epilepsia|May 19, 2015
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcomeBronwyn E Grinton, Sarah E Heron, James T Pelekanos, et al.
Brain : a Journal of Neurology|March 10, 2007
The spectrum of SCN1A-related infantile epileptic encephalopathiesLouise A Harkin, Jacinta M McMahon, Xenia Iona, et al.
Neurology|May 26, 2021
Association of <i>SLC32A1</i> Missense Variants With Genetic Epilepsy With Febrile Seizures PlusSarah E Heron, Brigid M Regan, Rebekah V Harris, et al.
American Journal of Human Genetics|January 17, 2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndromeSarah E Heron, Bronwyn E Grinton, Sara Kivity, et al.
The Journal of Antimicrobial Chemotherapy|December 3, 2013
Effect of clarithromycin in patients with suspected Gram-negative sepsis: results of a randomized controlled trialEvangelos J Giamarellos-Bourboulis, Vassiliki Mylona, Anastasia Antonopoulou, et al.
BMJ Open|July 15, 2017
PREDICT-CP: study protocol of implementation of comprehensive surveillance to predict outcomes for school-aged children with cerebral palsyRoslyn N Boyd, Peter Sw Davies, Jenny Ziviani, et al.
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