David A. Ramsay
London, ON, Canada
Last Updated: 09/26/2026
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Found 13 publications
A Case of Malignant Cerebral Edema Following Removal of Infected Autologous Cranioplasty Flap.
Journal: Journal of neurosurgical anesthesiology
Published: July 06, 2019
Leptomeningeal metastasis of classical Hodgkin lymphoma in a patient with malignant posterior reversible encephalopathy syndrome.
Journal: The Lancet. Oncology
Published: March 13, 2019
Intrasellar cavernous hemangioma presenting as pituitary adenoma: A report of two cases and review of the literature.
Journal: Clinical neuropathology
Published: December 01, 2017
Balo's concentric lesions with concurrent features of Schilder's disease in relapsing multiple sclerosis: neuropathological findings.
Journal: Autopsy & case reports
Published: October 23, 2016
Pathology of toxic leucoencephalopathy in drug abuse supports hypoxic-ischemic pathophysiology/etiology.
Journal: Neuropathology : official journal of the Japanese Society of Neuropathology
Published: October 19, 2016
Cerebellar liponeurocytoma: a rare intracranial tumor with possible familial predisposition. Case report.
Journal: Journal of neurosurgery
Published: November 28, 2015
Molecular subgroups of atypical teratoid rhabdoid tumours in children: an integrated genomic and clinicopathological analysis.
Journal: The Lancet. Oncology
Published: April 18, 2015
Case of multiple sulfatase deficiency and ocular albinism: a diagnostic odyssey.
Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: November 07, 2014
MELAS: A Multigenerational Impact of the MTTL1 A3243G MELAS Mutation.
Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: February 19, 2014
Exome sequencing identifies NFS1 deficiency in a novel Fe-S cluster disease, infantile mitochondrial complex II/III deficiency.
Journal: Molecular genetics & genomic medicine
Published: August 26, 2013
Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations.
Journal: Nature genetics
Published: April 24, 2013
Last Updated: 09/26/2026