Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Francesca Brett

Showing results (31-40 of 44) with videos related to

Pageof 5
Sort By:
Cancer Genetics|August 3, 2014
Rhabdoid tumor: the Irish experience 1986-2013Alice 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 Variant1Luke 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 experienceConor 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 impairmentJillian P Casey, Svein I Støve, Catherine McGorrian, et al.
Journal of Neurology|February 27, 2024
POLR3A-related disorders: expanding the clinical phenotypeMary 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 geneDiana 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 geneDiana 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 monitoringKate Connor, Emer Conroy, Kieron White, et al.
Biomolecules|February 16, 2020
Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob DiseaseFranc 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 sclerosisRobert J Carton, Michael G Doyle, Hugh Kearney, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Cancer Genetics|August 3, 2014
Rhabdoid tumor: the Irish experience 1986-2013Alice 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 Variant1Luke 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 experienceConor 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 impairmentJillian P Casey, Svein I Støve, Catherine McGorrian, et al.
Journal of Neurology|February 27, 2024
POLR3A-related disorders: expanding the clinical phenotypeMary 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 geneDiana 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 geneDiana 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 monitoringKate Connor, Emer Conroy, Kieron White, et al.
Biomolecules|February 16, 2020
Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob DiseaseFranc 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 sclerosisRobert J Carton, Michael G Doyle, Hugh Kearney, et al.
Pageof 5