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Journal of Child Neurology|October 5, 2020
Chudley-McCullough Syndrome: A Recognizable Clinical Entity Characterized by Deafness and Typical Brain MalformationsAglaë Blauen, Chloe A Stutterd, Katrien Stouffs, et al.
Scientific Reports|May 16, 2018
Generation and characterisation of a parkin-Pacrg knockout mouse line and a Pacrg knockout mouse lineSarah E M Stephenson, Timothy D Aumann, Juliet M Taylor, et al.
Human Molecular Genetics|October 11, 2002
Functional association of the parkin gene promoter with idiopathic Parkinson's diseaseAndrew B West, Demetrius Maraganore, Julia Crook, et al.
Neuron|December 24, 2002
Parkin protects against the toxicity associated with mutant alpha-synuclein: proteasome dysfunction selectively affects catecholaminergic neuronsLeonard Petrucelli, Casey O'Farrell, Paul J Lockhart, et al.
Developmental Medicine and Child Neurology|February 16, 2020
Callosal agenesis and congenital mirror movements: outcomes associated with DCC mutationsMegan Spencer-Smith, Jacquelyn L Knight, Emmanuelle Lacaze, et al.
Fertility and Sterility|March 10, 2009
Molecular analysis of the PArkin co-regulated gene and association with male infertilityGabrielle R Wilson, Marcus L-J Sim, Kate M Brody, et al.
Behavioral and Brain Functions : BBF|May 30, 2012
The COMT Val158 allele is associated with impaired delayed-match-to-sample performance in ADHDNatasha Matthews, Alasdair Vance, Tarrant D R Cummins, et al.
Epilepsia Open|December 3, 2022
Basal ganglia dysplasia and mTORopathy: A potential cause of postoperative seizures in focal cortical dysplasiaWei Shern Lee, Emma Macdonald-Laurs, Sarah E M Stephenson, et al.
Stem Cell Research|January 4, 2019
Generation of iPSC lines from peripheral blood mononuclear cells from 5 healthy adultsKaterina Vlahos, Koula Sourris, Robyn Mayberry, et al.
Epilepsy Research|March 4, 2021
Resection of tuber centers only for seizure control in tuberous sclerosis complexSarah E M Stephenson, Wirginia J Maixner, Sarah M Barton, et al.
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