E Byrne|S Marzuki|X Dennett - JoVE Visualize

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The Medical Journal of Australia|July 4, 1988

Current perspectives in the study of human mitochondriopathiesE Byrne, S Marzuki, X Dennett

Acta Neuropathologica|January 1, 1991

Chronic progressive external ophthalmoplegia in patients with large heteroplasmic mitochondrial DNA deletions: an immunocytochemical studyS Collins, X Dennett, E Byrne, et al.

Neurology|September 1, 1987

Mitochondrial studies in Kearns-Sayre syndrome: normal respiratory chain function with absence of a mitochondrial translation productE Byrne, S Marzuki, N Sattayasai, et al.

Biochimica Et Biophysica Acta|November 21, 1991

Mitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNAS Collins, C Rudduck, S Marzuki, et al.

Biochemical Medicine and Metabolic Biology|August 1, 1991

Affinity chromatography isolation of human cytochrome oxidase and small-scale Western immunoblot probing of the enzyme complex in mitochondrial cytopathy patientsI Trounce, E Byrne, X Dennett, et al.

Journal of the Neurological Sciences|December 1, 1988

Progression from MERRF to MELAS phenotype in a patient with combined respiratory complex I and IV deficienciesE Byrne, I Trounce, X Dennett, et al.

Australian and New Zealand Journal of Medicine|December 1, 1991

Biochemical and molecular investigation of mitochondrial disease: an illustrative case showing the value of a multifaceted approachE Byrne, B Jean-Francois, D Thyagarajan, et al.

Mutation Research|September 1, 1992

Respiratory chain failure in adult muscle fibres: relationship with ageing and possible implications for the neuronal poolE Byrne, X Dennett

Journal of the Neurological Sciences|March 1, 1991

Functional respiratory chain studies in subjects with chronic progressive external ophthalmoplegia and large heteroplasmic mitochondrial DNA deletionsI Trounce, E Byrne, S Marzuki, et al.

Acta Neuropathologica|January 1, 1991

Functional respiratory chain studies in mitochondrial cytopathies. Support for mitochondrial DNA heteroplasmy in myoclonus epilepsy and ragged red fibers (MERRF) syndromeE Byrne, I Trounce, S Marzuki, et al.

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Showing results (1-10 of 589) with videos related to

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Pageof 59

The Medical Journal of Australia|July 4, 1988

Current perspectives in the study of human mitochondriopathiesE Byrne, S Marzuki, X Dennett

Acta Neuropathologica|January 1, 1991

Chronic progressive external ophthalmoplegia in patients with large heteroplasmic mitochondrial DNA deletions: an immunocytochemical studyS Collins, X Dennett, E Byrne, et al.

Neurology|September 1, 1987

Mitochondrial studies in Kearns-Sayre syndrome: normal respiratory chain function with absence of a mitochondrial translation productE Byrne, S Marzuki, N Sattayasai, et al.

Biochimica Et Biophysica Acta|November 21, 1991

Mitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNAS Collins, C Rudduck, S Marzuki, et al.

Biochemical Medicine and Metabolic Biology|August 1, 1991

Affinity chromatography isolation of human cytochrome oxidase and small-scale Western immunoblot probing of the enzyme complex in mitochondrial cytopathy patientsI Trounce, E Byrne, X Dennett, et al.

Journal of the Neurological Sciences|December 1, 1988

Progression from MERRF to MELAS phenotype in a patient with combined respiratory complex I and IV deficienciesE Byrne, I Trounce, X Dennett, et al.

Australian and New Zealand Journal of Medicine|December 1, 1991

Biochemical and molecular investigation of mitochondrial disease: an illustrative case showing the value of a multifaceted approachE Byrne, B Jean-Francois, D Thyagarajan, et al.

Mutation Research|September 1, 1992

Respiratory chain failure in adult muscle fibres: relationship with ageing and possible implications for the neuronal poolE Byrne, X Dennett

Journal of the Neurological Sciences|March 1, 1991

Functional respiratory chain studies in subjects with chronic progressive external ophthalmoplegia and large heteroplasmic mitochondrial DNA deletionsI Trounce, E Byrne, S Marzuki, et al.

Acta Neuropathologica|January 1, 1991

Functional respiratory chain studies in mitochondrial cytopathies. Support for mitochondrial DNA heteroplasmy in myoclonus epilepsy and ragged red fibers (MERRF) syndromeE Byrne, I Trounce, S Marzuki, et al.

Pageof 59