Search research articles
Contact Us
Filters
Showing results (131-140 of 473) with videos related to
Page
of 48
Sort By:
Brain : a Journal of Neurology
|
April 6, 2015
Reply: Evaluation of exome sequencing variation in undiagnosed ataxias
Angela Pyle, Helen Griffin, Michael J Keogh, et al.
Annals of Neurology
|
May 4, 2004
Molecular epidemiology of spinocerebellar ataxia type 6
Kate Craig, Sharon M Keers, Kate Archibald, et al.
Nature Reviews. Drug Discovery
|
April 27, 2023
Opportunities for mitochondrial disease gene therapy
Carlo Viscomi, Jelle van den Ameele, Kathrin C Meyer, et al.
Neurogenetics
|
January 27, 2012
Neuroferritinopathy: a new inborn error of iron metabolism
Michael J Keogh, Patricia Jonas, Alan Coulthard, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Clinical Manifestations
Md Shafiqur Rahman, Timothy Rittman, Brian D M Tom, et al.
Neurology
|
September 6, 2015
Prevalence of neurogenetic disorders in the North of England
David Bargiela, Patrick Yu-Wai-Man, Michael Keogh, et al.
Nucleic Acids Research
|
December 1, 2021
Single-molecule mitochondrial DNA sequencing shows no evidence of CpG methylation in human cells and tissues
Iacopo Bicci, Claudia Calabrese, Zoe J Golder, et al.
Molecular Vision
|
November 5, 2004
Apolipoprotein E promoter polymorphisms do not have a major influence on the risk of developing primary open angle glaucoma
Thomas Ressiniotis, Philip G Griffiths, Michael Birch, et al.
BMC Ophthalmology
|
April 6, 2005
A polymorphism at codon 31 of gene p21 is not associated with primary open angle glaucoma in Caucasians
Thomas Ressiniotis, Philip G Griffiths, Sharon M Keers, et al.
Seminars in Cell & Developmental Biology
|
October 16, 2019
Mitochondrial heteroplasmy beyond the oocyte bottleneck
Jelle van den Ameele, Andy Y Z Li, Hansong Ma, et al.
Page
of 48
Search research articles
Search
Showing results (131-140 of 473) with videos related to
Sort By:
Page
of 48
Brain : a Journal of Neurology
|
April 6, 2015
Reply: Evaluation of exome sequencing variation in undiagnosed ataxias
Angela Pyle, Helen Griffin, Michael J Keogh, et al.
Annals of Neurology
|
May 4, 2004
Molecular epidemiology of spinocerebellar ataxia type 6
Kate Craig, Sharon M Keers, Kate Archibald, et al.
Nature Reviews. Drug Discovery
|
April 27, 2023
Opportunities for mitochondrial disease gene therapy
Carlo Viscomi, Jelle van den Ameele, Kathrin C Meyer, et al.
Neurogenetics
|
January 27, 2012
Neuroferritinopathy: a new inborn error of iron metabolism
Michael J Keogh, Patricia Jonas, Alan Coulthard, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Clinical Manifestations
Md Shafiqur Rahman, Timothy Rittman, Brian D M Tom, et al.
Neurology
|
September 6, 2015
Prevalence of neurogenetic disorders in the North of England
David Bargiela, Patrick Yu-Wai-Man, Michael Keogh, et al.
Nucleic Acids Research
|
December 1, 2021
Single-molecule mitochondrial DNA sequencing shows no evidence of CpG methylation in human cells and tissues
Iacopo Bicci, Claudia Calabrese, Zoe J Golder, et al.
Molecular Vision
|
November 5, 2004
Apolipoprotein E promoter polymorphisms do not have a major influence on the risk of developing primary open angle glaucoma
Thomas Ressiniotis, Philip G Griffiths, Michael Birch, et al.
BMC Ophthalmology
|
April 6, 2005
A polymorphism at codon 31 of gene p21 is not associated with primary open angle glaucoma in Caucasians
Thomas Ressiniotis, Philip G Griffiths, Sharon M Keers, et al.
Seminars in Cell & Developmental Biology
|
October 16, 2019
Mitochondrial heteroplasmy beyond the oocyte bottleneck
Jelle van den Ameele, Andy Y Z Li, Hansong Ma, et al.
Page
of 48