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Epilepsy Research|February 14, 2017
SCN1A clinical spectrum includes the self-limited focal epilepsies of childhoodSara Kivity, Karen L Oliver, Zaid Afawi, et al.Epilepsia|January 14, 2017
De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndromeKenneth A Myers, Rosemary Burgess, Zaid Afawi, et al.Epilepsy Research|April 19, 2017
Evaluation of GLUT1 variation in non-acquired focal epilepsyAlexander Peeraer, John A Damiano, Susannah T Bellows, et al.Epilepsia|January 19, 2017
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrumJohn A Damiano, Rosemary Burgess, Sara Kivity, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|December 21, 2017
Sensitive quantitative detection of somatic mosaic mutation in "double cortex" syndromeJohn A Damiano, Hongdo Do, Ezgi Ozturk, et al.Epilepsia|July 6, 2018
Evidence of linkage to chromosome 5p13.2-q11.1 in a large inbred family with genetic generalized epilepsyDemet Kinay, Karen L Oliver, Erdem Tüzün, et al.Epilepsia|February 4, 2014
Glucose metabolism transporters and epilepsy: only GLUT1 has an established roleMichael S Hildebrand, John A Damiano, Saul A Mullen, et al.Developmental Medicine and Child Neurology|June 7, 2016
Evaluation of non-coding variation in GLUT1 deficiencyYu-Chi Liu, Jia Wei Audrey Lee, Susannah T Bellows, et al.Epilepsia|April 11, 2023
Recognition and epileptology of protracted CLN3 diseaseJillian M Cameron, John A Damiano, Bronwyn Grinton, et al.Annals of Neurology|January 3, 2013
Glucose transporter 1 deficiency in the idiopathic generalized epilepsiesTodor Arsov, Saul A Mullen, Sue Rogers, et al.Pageof 4