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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

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Andrew M Schaefer

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Movement Disorders : Official Journal of the Movement Disorder Society|August 13, 2015

Adult-onset myoclonus ataxia associated with the mitochondrial m.8993T>C "NARP" mutationMika H Martikainen, Grainne S Gorman, Paul Goldsmith, et al.

Journal of Medical Genetics|September 5, 2006

Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutationAngela Pyle, Robert W Taylor, Steve E Durham, et al.

BMJ Neurology Open|December 15, 2022

Changing faces of mitochondrial disease: autosomal recessive <i>POLG</i> disease mimicking myasthenia gravis and progressive supranuclear palsyMenatalla Elwan, Andrew M Schaefer, Kate Craig, et al.

European Journal of Human Genetics : EJHG|June 17, 2004

Noninvasive diagnosis of the 3243A > G mitochondrial DNA mutation using urinary epithelial cellsMartina T McDonnell, Andrew M Schaefer, Emma L Blakely, et al.

Brain : a Journal of Neurology|November 7, 2006

Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletionsTanja Taivassalo, Julie L Gardner, Robert W Taylor, et al.

Annals of Neurology|September 22, 2007

Prevalence of mitochondrial DNA disease in adultsAndrew M Schaefer, Robert McFarland, Emma L Blakely, et al.

Neurology. Clinical Practice|April 12, 2021

Neuromuscular Junction Abnormalities in Mitochondrial Disease: An Observational Cohort StudyLuis P Braz, Yi Shiau Ng, Gráinne S Gorman, et al.

Brain : a Journal of Neurology|November 6, 2008

Resistance training in patients with single, large-scale deletions of mitochondrial DNAJulie L Murphy, Emma L Blakely, Andrew M Schaefer, et al.

The FEBS Journal|July 13, 2005

A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeastEmma L Blakely, Anna L Mitchell, Nicholas Fisher, et al.

Archives of Neurology|April 11, 2007

Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and ParkinsonismGavin Hudson, Andrew M Schaefer, Robert W Taylor, et al.

Pageof 6

Search research articles

Showing results (11-20 of 60) with videos related to

Sort By:

Pageof 6

Movement Disorders : Official Journal of the Movement Disorder Society|August 13, 2015

Adult-onset myoclonus ataxia associated with the mitochondrial m.8993T>C "NARP" mutationMika H Martikainen, Grainne S Gorman, Paul Goldsmith, et al.

Journal of Medical Genetics|September 5, 2006

Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutationAngela Pyle, Robert W Taylor, Steve E Durham, et al.

BMJ Neurology Open|December 15, 2022

Changing faces of mitochondrial disease: autosomal recessive <i>POLG</i> disease mimicking myasthenia gravis and progressive supranuclear palsyMenatalla Elwan, Andrew M Schaefer, Kate Craig, et al.

European Journal of Human Genetics : EJHG|June 17, 2004

Noninvasive diagnosis of the 3243A > G mitochondrial DNA mutation using urinary epithelial cellsMartina T McDonnell, Andrew M Schaefer, Emma L Blakely, et al.

Brain : a Journal of Neurology|November 7, 2006

Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletionsTanja Taivassalo, Julie L Gardner, Robert W Taylor, et al.

Annals of Neurology|September 22, 2007

Prevalence of mitochondrial DNA disease in adultsAndrew M Schaefer, Robert McFarland, Emma L Blakely, et al.

Neurology. Clinical Practice|April 12, 2021

Neuromuscular Junction Abnormalities in Mitochondrial Disease: An Observational Cohort StudyLuis P Braz, Yi Shiau Ng, Gráinne S Gorman, et al.

Brain : a Journal of Neurology|November 6, 2008

Resistance training in patients with single, large-scale deletions of mitochondrial DNAJulie L Murphy, Emma L Blakely, Andrew M Schaefer, et al.

The FEBS Journal|July 13, 2005

A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeastEmma L Blakely, Anna L Mitchell, Nicholas Fisher, et al.

Archives of Neurology|April 11, 2007

Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and ParkinsonismGavin Hudson, Andrew M Schaefer, Robert W Taylor, et al.

Pageof 6