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Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.
Brain. 2015 Oct;138(Pt 10):2859-74. doi: 10.1093/brain/awv243. Epub 2015 Aug 21.
Brain. 2015.
PMID: 26297560
Free PMC article.
Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy.
Bagnall RD, Crompton DE, Petrovski S, Lam L, Cutmore C, Garry SI, Sadleir LG, Dibbens LM, Cairns A, Kivity S, Afawi Z, Regan BM, Duflou J, Berkovic SF, Scheffer IE, Semsarian C.
Bagnall RD, et al. Among authors: garry si.
Ann Neurol. 2016 Apr;79(4):522-34. doi: 10.1002/ana.24596. Epub 2016 Feb 2.
Ann Neurol. 2016.
PMID: 26704558
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EXOME REPORT: Novel mutation in ATP6V1B2 segregating with autosomal dominant epilepsy, intellectual disability and mild gingival and nail abnormalities.
Shaw M, Winczewska-Wiktor A, Badura-Stronka M, Koirala S, Gardner A, Kuszel Ł, Kowal P, Steinborn B, Starczewska M, Garry S, Scheffer IE, Berkovic SF, Gecz J.
Shaw M, et al.
Eur J Med Genet. 2020 Apr;63(4):103799. doi: 10.1016/j.ejmg.2019.103799. Epub 2019 Oct 23.
Eur J Med Genet. 2020.
PMID: 31655144
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Transient Treg-cell depletion in adult mice results in persistent self-reactive CD4(+) T-cell responses.
Nyström SN, Bourges D, Garry S, Ross EM, van Driel IR, Gleeson PA.
Nyström SN, et al.
Eur J Immunol. 2014 Dec;44(12):3621-31. doi: 10.1002/eji.201344432. Epub 2014 Nov 2.
Eur J Immunol. 2014.
PMID: 25231532
Free article.
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