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Harefuah|September 26, 2008
[Referral letters to the pediatric emergency department]Simon Edvardson, Talya DorHarefuah|March 28, 2018
[EXOME ANALYSIS - A GAME CHANGER IN PEDIATRICS]Asaf Ta-Shma, Simon Edvardson, Orly Elpeleg, et al.Lipids in Health and Disease|May 24, 2011
2-Hydroxylated sphingomyelin profiles in cells from patients with mutated fatty acid 2-hydroxylasePhyllis Dan, Simon Edvardson, Jacek Bielawski, et al.Annals of Neurology|February 29, 2008
Mitochondrial complex I deficiency caused by a deleterious NDUFA11 mutationItai Berger, Eli Hershkovitz, Avraham Shaag, et al.Epilepsia|June 14, 2012
Intractable epilepsy of infancy due to homozygous mutation in the EFHC1 geneItai Berger, Talya Dor, Jonatan Halvardson, et al.Journal of Medical Genetics|July 2, 2013
West syndrome, microcephaly, grey matter heterotopia and hypoplasia of corpus callosum due to a novel ARFGEF2 mutationEhud Banne, Osama Atawneh, Marco Henneke, et al.Neurology|May 18, 2012
Highly fatal fast-channel syndrome caused by AChR ε subunit mutation at the agonist binding siteXin-Ming Shen, Joan M Brengman, Simon Edvardson, et al.Neurogenetics|May 12, 2017
Hypomyelinating leukodystrophy associated with a deleterious mutation in the ATRN geneMaher Awni Shahrour, Motee Ashhab, Simon Edvardson, et al.Annals of Neurology|April 24, 2012
Hereditary sensory autonomic neuropathy caused by a mutation in dystoninSimon Edvardson, Yuval Cinnamon, Chaim Jalas, et al.Molecular Genetics and Metabolism|January 9, 2008
The unique neuroradiology of complex I deficiency due to NDUFA12L defectFlora Barghuti, Khaled Elian, John Moshe Gomori, et al.Pageof 8