Search research articles
Contact Us
Filters
Showing results (21-30 of 37) with videos related to
Page
of 4
Sort By:
Clinical Neuropathology
|
March 27, 2023
Brain biopsy in neurological disease of unknown etiology: A single-center 12-year retrospective analysis
Andrew Lockhart, Josephine Heffernan, Ann Kennedy, et al.
Movement Disorders Clinical Practice
|
August 18, 2021
Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by <i>MAPT</i> Variants
Laura Williams, Diana A Olszewska, Conor Fearon, et al.
Irish Journal of Medical Science
|
December 5, 2019
Impact of the 2016 World Health Organization Classification of Tumours of the Central Nervous System: an Irish experience
Conor Fearon, Teresa Loftus, Amber Lynn Byrne, et al.
Purinergic Signalling
|
July 2, 2025
The CALHM1 blocker CGP37157 increases seizure severity during status epilepticus in adult mice
Meghma Mitra, Amaya Sanz Rodriguez, Norman Delanty, et al.
The American Journal of Case Reports
|
July 1, 2020
A Surviving Case of Acanthamoeba Granulomatous Amebic Encephalitis in a Hematopoietic Stem Cell Transplant Recipient
Niamh A Keane, Louise Marie Lane, Emma Canniff, et al.
Clinical Neuropathology
|
March 31, 2026
Retrospective neuropathologic analysis of adult spinal tumors in a single neuroscience center 2018 - 2023
Ciara O'Donoghue, Beibhinn Wilkins, Alan Beausang, et al.
Epilepsia
|
June 3, 2022
MicroRNA inhibition using antimiRs in acute human brain tissue sections
Gareth Morris, Elena Langa, Conor Fearon, et al.
Neurobiology of Aging
|
September 24, 2024
Corrigendum to: A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10 G>T at the intron 9/exon 10 of the MAPT gene
Diana A Olszewska, Conor Fearon, Christopher McGuigan, et al.
Neurobiology of Aging
|
July 18, 2021
A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene
Diana A Olszewska, Conor Fearon, Christopher McGuigan, et al.
Nature Communications
|
April 15, 2022
Microvascular stabilization via blood-brain barrier regulation prevents seizure activity
Chris Greene, Nicole Hanley, Cristina R Reschke, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
Clinical Neuropathology
|
March 27, 2023
Brain biopsy in neurological disease of unknown etiology: A single-center 12-year retrospective analysis
Andrew Lockhart, Josephine Heffernan, Ann Kennedy, et al.
Movement Disorders Clinical Practice
|
August 18, 2021
Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by <i>MAPT</i> Variants
Laura Williams, Diana A Olszewska, Conor Fearon, et al.
Irish Journal of Medical Science
|
December 5, 2019
Impact of the 2016 World Health Organization Classification of Tumours of the Central Nervous System: an Irish experience
Conor Fearon, Teresa Loftus, Amber Lynn Byrne, et al.
Purinergic Signalling
|
July 2, 2025
The CALHM1 blocker CGP37157 increases seizure severity during status epilepticus in adult mice
Meghma Mitra, Amaya Sanz Rodriguez, Norman Delanty, et al.
The American Journal of Case Reports
|
July 1, 2020
A Surviving Case of Acanthamoeba Granulomatous Amebic Encephalitis in a Hematopoietic Stem Cell Transplant Recipient
Niamh A Keane, Louise Marie Lane, Emma Canniff, et al.
Clinical Neuropathology
|
March 31, 2026
Retrospective neuropathologic analysis of adult spinal tumors in a single neuroscience center 2018 - 2023
Ciara O'Donoghue, Beibhinn Wilkins, Alan Beausang, et al.
Epilepsia
|
June 3, 2022
MicroRNA inhibition using antimiRs in acute human brain tissue sections
Gareth Morris, Elena Langa, Conor Fearon, et al.
Neurobiology of Aging
|
September 24, 2024
Corrigendum to: A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10 G>T at the intron 9/exon 10 of the MAPT gene
Diana A Olszewska, Conor Fearon, Christopher McGuigan, et al.
Neurobiology of Aging
|
July 18, 2021
A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene
Diana A Olszewska, Conor Fearon, Christopher McGuigan, et al.
Nature Communications
|
April 15, 2022
Microvascular stabilization via blood-brain barrier regulation prevents seizure activity
Chris Greene, Nicole Hanley, Cristina R Reschke, et al.
Page
of 4