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Neurology|August 22, 2014
Rasmussen encephalitis and comorbid autoimmune diseases: A window into disease mechanism?Dina Amrom, Demet Kinay, Yvonne Hart, et al.
American Journal of Medical Genetics. Part A|October 30, 2019
Duplication 2p16 is associated with perisylvian polymicrogyriaDina Amrom, Annapurna Poduri, Jennifer S Goldman, et al.
Clinical & Developmental Immunology|November 24, 2004
Autoimmune epilepsy: some epilepsy patients harbor autoantibodies to glutamate receptors and dsDNA on both sides of the blood-brain barrier, which may kill neurons and decrease in brain fluids after hemispherotomyYonatan Ganor, Hadassa Goldberg-Stern, Dina Amrom, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Möbius sequence, Robin complex, and hypotonia: severe expression of brainstem disruption spectrum versus Carey-Fineman-Ziter syndromeAlain Verloes, Pierre Bitoun, Anne Heuskin, et al.
Journal of Medical Genetics|September 27, 2012
Mutations in TMEM231 cause Joubert syndrome in French CanadiansMyriam Srour, Fadi F Hamdan, Jeremy A Schwartzentruber, et al.
Annals of Neurology|February 11, 2026
Diverse Genetic Etiologies of Unilateral PolymicrogyriaAbbe Lai, Jennifer E Neil, Shyam K Akula, et al.
Neurogenetics|January 6, 2012
Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new casesJill A Rosenfeld, Dina Amrom, Eva Andermann, et al.
Nature Reviews. Neurology|September 8, 2020
International consensus recommendations on the diagnostic work-up for malformations of cortical developmentRenske Oegema, Tahsin Stefan Barakat, Martina Wilke, et al.
Neuron|August 28, 2018
Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor DevelopmentRichard S Smith, Connor J Kenny, Vijay Ganesh, et al.
Molecular Psychiatry|June 30, 2021
Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neuronsKaren Runge, Rémi Mathieu, Stéphane Bugeon, et al.
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