Bernard Rosenblatt
Montreal, QC, Canada
Last Updated: 09/26/2026
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Found 15 publications
The Experience of Parents of Children With Genetically Determined Leukoencephalopathies With the Health Care System: A Qualitative Study.
Journal: Journal of child neurology
Published: May 24, 2023
mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development: Novel Variants, Topographic Mapping, and Clinical Outcomes.
Journal: Neurology. Genetics
Published: April 21, 2023
Surgically Remediable Secondary Network Epileptic Encephalopathies With Continuous Spike Wave in Sleep: Lesions May Not Be Visible on Brain Magnetic Resonance Imaging (MRI).
Journal: Journal of child neurology
Published: October 03, 2022
Experience of Parents of Children with Genetically Determined Leukoencephalopathies Regarding the Adapted Health Care Services During the COVID-19 Pandemic.
Journal: Journal of child neurology
Published: January 05, 2022
New interinstitutional, multimodal presurgical evaluation protocol associated with improved seizure freedom for poorly defined cases of focal epilepsy in children.
Journal: Journal of neurosurgery. Pediatrics
Published: January 08, 2021
Overnight Ictal Magnetoencephalography.
Journal: Neurology. Clinical practice
Published: February 18, 2020
DCC Is Required for the Development of Nociceptive Topognosis in Mice and Humans.
Journal: Cell reports
Published: September 18, 2017
Clinical and Radiologic Spectrum of Septo-optic Dysplasia: Review of 17 Cases.
Journal: Journal of child neurology
Published: May 10, 2017
Breaking the cycle: A comparison between intravenous immunoglobulins and high dosage prednisone in the treatment of medically intractable epilepsy in children.
Journal: Seizure
Published: October 12, 2016
Somatosensory evoked potentials in neonates with hypoxic-ischemic encephalopathy treated with hypothermia.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: October 28, 2014
De novo deletion of FMN2 in a girl with mild non-syndromic intellectual disability.
Journal: European journal of medical genetics
Published: March 05, 2013
Last Updated: 09/26/2026