Esther Ganelin‐Cohen

Disease Course and Treatment Responses in Children With Relapsing Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease

Yael Hacohen, Yu Yi M. Wong, Christian Lechner et al. · JAMA Neurology · 2018 · 403 citations · Full text

<i><scp>SLC1A4</scp></i> mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum

Gali Heimer, Dina Marek‐Yagel, Eran Eyal et al. · Clinical Genetics · 2015 · 56 citations

CAOS—Episodic Cerebellar Ataxia, Areflexia, Optic Atrophy, and Sensorineural Hearing Loss

Gali Heimer, Yair Sadaka, Lori Israelian et al. · Journal of Child Neurology · 2015 · 52 citations

Acute Cerebellitis in Children

Liora Kornreich, Vered Shkalim‐Zemer, Yoel Levinsky et al. · Journal of Child Neurology · 2016 · 44 citations

Pediatric Hydrocephalus, Pediatric Neurosurgery, Neurological Disorder +10

Myelin oligodendrocyte glycoprotein-positive optic neuritis masquerading as pseudotumor cerebri at presentation

Itay Lotan, Judith Brody, Mark A. Hellmann et al. · Journal of Neurology · 2018 · 33 citations

Ophthalmology, Glycoprotein-positive Optic Neuritis, Optic Neuropathy +7