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Cancer Genetics
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August 3, 2014
Rhabdoid tumor: the Irish experience 1986-2013
Alice Uwineza, Harinder Gill, Patrick Buckley, et al.
Journal of Neuromuscular Diseases
|
April 21, 2020
Chronic Progressive External Ophthalmoplegia due to a Rare de novo m.12334G>A MT-TL2 Mitochondrial DNA Variant1
Luke O'Donnell, Emma L Blakely, Karen Baty, 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.
Scientific Reports
|
November 3, 2015
NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment
Jillian P Casey, Svein I Støve, Catherine McGorrian, et al.
Journal of Neurology
|
February 27, 2024
POLR3A-related disorders: expanding the clinical phenotype
Mary Clare McKenna, Antoinette O'Connor, Andrew Lockhart, 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.
Scientific Reports
|
February 1, 2024
A clinically relevant computed tomography (CT) radiomics strategy for intracranial rodent brain tumour monitoring
Kate Connor, Emer Conroy, Kieron White, et al.
Biomolecules
|
February 16, 2020
Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob Disease
Franc Llorens, Anna Villar-Piqué, Peter Hermann, et al.
Epilepsia
|
March 16, 2024
Somatic variants as a cause of drug-resistant epilepsy including mesial temporal lobe epilepsy with hippocampal sclerosis
Robert J Carton, Michael G Doyle, Hugh Kearney, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 44) with videos related to
Sort By:
Page
of 5
Cancer Genetics
|
August 3, 2014
Rhabdoid tumor: the Irish experience 1986-2013
Alice Uwineza, Harinder Gill, Patrick Buckley, et al.
Journal of Neuromuscular Diseases
|
April 21, 2020
Chronic Progressive External Ophthalmoplegia due to a Rare de novo m.12334G>A MT-TL2 Mitochondrial DNA Variant1
Luke O'Donnell, Emma L Blakely, Karen Baty, 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.
Scientific Reports
|
November 3, 2015
NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment
Jillian P Casey, Svein I Støve, Catherine McGorrian, et al.
Journal of Neurology
|
February 27, 2024
POLR3A-related disorders: expanding the clinical phenotype
Mary Clare McKenna, Antoinette O'Connor, Andrew Lockhart, 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.
Scientific Reports
|
February 1, 2024
A clinically relevant computed tomography (CT) radiomics strategy for intracranial rodent brain tumour monitoring
Kate Connor, Emer Conroy, Kieron White, et al.
Biomolecules
|
February 16, 2020
Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob Disease
Franc Llorens, Anna Villar-Piqué, Peter Hermann, et al.
Epilepsia
|
March 16, 2024
Somatic variants as a cause of drug-resistant epilepsy including mesial temporal lobe epilepsy with hippocampal sclerosis
Robert J Carton, Michael G Doyle, Hugh Kearney, et al.
Page
of 5