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Neurology
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April 30, 2008
T2* and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation
A McNeill, D Birchall, S J Hayflick, et al.
Trends in Genetics : TIG
|
November 14, 2000
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?
P F Chinnery, D R Thorburn, D C Samuels, et al.
Mitochondrion
|
July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathy
A Majander, A G Robson, C João, et al.
Neurology
|
April 23, 2003
Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)
A Agostino, L Valletta, P F Chinnery, et al.
Journal of Medical Genetics
|
June 7, 2007
Mitochondrial DNA haplogroups and type 2 diabetes: a study of 897 cases and 1010 controls
P F Chinnery, C Mowbray, S K Patel, et al.
Journal of Neurology
|
July 5, 2015
Voxel-based analysis in neuroferritinopathy expands the phenotype and determines radiological correlates of disease severity
M J Keogh, B S Aribisala, J He, et al.
Journal of Neurology
|
May 16, 2015
Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia
M J Keogh, H Steele, K Douroudis, et al.
Brain : a Journal of Neurology
|
January 3, 2001
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy
P F Chinnery, D T Brown, R M Andrews, et al.
Neurology
|
May 10, 2006
POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions
G Hudson, M Deschauer, R W Taylor, et al.
Neurology
|
February 11, 2009
Urine heteroplasmy is the best predictor of clinical outcome in the m.3243A>G mtDNA mutation
R G Whittaker, J K Blackwood, C L Alston, et al.
Page
of 16
Search research articles
Search
Showing results (111-120 of 152) with videos related to
Sort By:
Page
of 16
Neurology
|
April 30, 2008
T2* and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation
A McNeill, D Birchall, S J Hayflick, et al.
Trends in Genetics : TIG
|
November 14, 2000
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?
P F Chinnery, D R Thorburn, D C Samuels, et al.
Mitochondrion
|
July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathy
A Majander, A G Robson, C João, et al.
Neurology
|
April 23, 2003
Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)
A Agostino, L Valletta, P F Chinnery, et al.
Journal of Medical Genetics
|
June 7, 2007
Mitochondrial DNA haplogroups and type 2 diabetes: a study of 897 cases and 1010 controls
P F Chinnery, C Mowbray, S K Patel, et al.
Journal of Neurology
|
July 5, 2015
Voxel-based analysis in neuroferritinopathy expands the phenotype and determines radiological correlates of disease severity
M J Keogh, B S Aribisala, J He, et al.
Journal of Neurology
|
May 16, 2015
Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia
M J Keogh, H Steele, K Douroudis, et al.
Brain : a Journal of Neurology
|
January 3, 2001
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy
P F Chinnery, D T Brown, R M Andrews, et al.
Neurology
|
May 10, 2006
POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions
G Hudson, M Deschauer, R W Taylor, et al.
Neurology
|
February 11, 2009
Urine heteroplasmy is the best predictor of clinical outcome in the m.3243A>G mtDNA mutation
R G Whittaker, J K Blackwood, C L Alston, et al.
Page
of 16