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European Heart Journal. Cardiovascular Imaging
|
November 7, 2012
Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriers
Matthew G D Bates, Kieren G Hollingsworth, Jane H Newman, et al.
Annals of Neurology
|
July 26, 2016
Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination
Yi Shiau Ng, Catherine Feeney, Andrew M Schaefer, et al.
Gastro Hep Advances
|
August 12, 2024
Phase II Feasibility Study of the Efficacy, Tolerability, and Impact on the Gut Microbiome of a Low-Residue (Fiber) Diet in Adult Patients With Mitochondrial Disease
David Houghton, Yi Shiau Ng, Matthew A Jackson, et al.
JAMA Neurology
|
November 25, 2014
Clonal expansion of secondary mitochondrial DNA deletions associated with spinocerebellar ataxia type 28
Gráinne S Gorman, Gerald Pfeffer, Helen Griffin, et al.
Neurology
|
November 8, 2013
Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions
Charlotte L Alston, Andrew M Schaefer, Pravrutha Raman, et al.
Neurology
|
May 4, 2018
Multifocal demyelinating motor neuropathy and hamartoma syndrome associated with a de novo <i>PTEN</i> mutation
Boglarka Bansagi, Vietxuan Phan, Mark R Baker, et al.
EMBO Molecular Medicine
|
May 9, 2018
mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease
John P Grady, Sarah J Pickett, Yi Shiau Ng, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 2011
Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3
Rita Horvath, Birgit Czermin, Sweena Gulati, et al.
Annals of Neurology
|
December 29, 2017
Pathological mechanisms underlying single large-scale mitochondrial DNA deletions
Mariana C Rocha, Hannah S Rosa, John P Grady, et al.
Molecular Cell
|
January 2, 2018
Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNA
Thomas J Nicholls, Cristina A Nadalutti, Elisa Motori, et al.
Page
of 30
Search research articles
Search
Showing results (241-250 of 299) with videos related to
Sort By:
Page
of 30
European Heart Journal. Cardiovascular Imaging
|
November 7, 2012
Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriers
Matthew G D Bates, Kieren G Hollingsworth, Jane H Newman, et al.
Annals of Neurology
|
July 26, 2016
Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination
Yi Shiau Ng, Catherine Feeney, Andrew M Schaefer, et al.
Gastro Hep Advances
|
August 12, 2024
Phase II Feasibility Study of the Efficacy, Tolerability, and Impact on the Gut Microbiome of a Low-Residue (Fiber) Diet in Adult Patients With Mitochondrial Disease
David Houghton, Yi Shiau Ng, Matthew A Jackson, et al.
JAMA Neurology
|
November 25, 2014
Clonal expansion of secondary mitochondrial DNA deletions associated with spinocerebellar ataxia type 28
Gráinne S Gorman, Gerald Pfeffer, Helen Griffin, et al.
Neurology
|
November 8, 2013
Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions
Charlotte L Alston, Andrew M Schaefer, Pravrutha Raman, et al.
Neurology
|
May 4, 2018
Multifocal demyelinating motor neuropathy and hamartoma syndrome associated with a de novo <i>PTEN</i> mutation
Boglarka Bansagi, Vietxuan Phan, Mark R Baker, et al.
EMBO Molecular Medicine
|
May 9, 2018
mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease
John P Grady, Sarah J Pickett, Yi Shiau Ng, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 2011
Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3
Rita Horvath, Birgit Czermin, Sweena Gulati, et al.
Annals of Neurology
|
December 29, 2017
Pathological mechanisms underlying single large-scale mitochondrial DNA deletions
Mariana C Rocha, Hannah S Rosa, John P Grady, et al.
Molecular Cell
|
January 2, 2018
Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNA
Thomas J Nicholls, Cristina A Nadalutti, Elisa Motori, et al.
Page
of 30