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Journal of Clinical Neuromuscular Disease
|
December 17, 2008
A novel clinical phenotype of myopathy, sensorimotor neuropathy, infertility, and hypogonadism with multiple mitochondrial DNA deletions
A Quigley, K Reardon, R Kapsa, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
April 1, 1997
Are mitochondrial DNA deletions causative in chronic progressive external ophthalmoplegia patients?
M J Jean-Francois, S Collins, N Kotsimbos, et al.
Australian and New Zealand Journal of Medicine
|
August 1, 1987
Chronic alcoholic proximal wasting: physiological, morphological and biochemical studies in skeletal muscle
I Trounce, E Byrne, X Dennett, et al.
Journal of Developmental Physiology
|
October 1, 1982
Function of the future respiratory system in the growth retarded fetal sheep
J E Maloney, G Bowes, V Brodecky, 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 deficiencies
E 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 approach
E Byrne, B Jean-Francois, D Thyagarajan, et al.
The Medical Journal of Australia
|
April 16, 1998
Polymyositis caused by a new genus of nematode
X Dennett, S J Siejka, J R Andrews, et al.
Archives of Neurology
|
August 1, 1986
Proximal motor neuropathy, dermato-endocrine syndrome, and IgG kappa paraproteinemia
S F Berkovic, J D Scarlett, G R Symington, et al.
Journal of the Neurological Sciences
|
March 1, 1991
Functional respiratory chain studies in subjects with chronic progressive external ophthalmoplegia and large heteroplasmic mitochondrial DNA deletions
I Trounce, E Byrne, S Marzuki, et al.
Neurology
|
April 24, 1999
Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder
D M Kirby, M Crawford, M A Cleary, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 59) with videos related to
Sort By:
Page
of 6
Journal of Clinical Neuromuscular Disease
|
December 17, 2008
A novel clinical phenotype of myopathy, sensorimotor neuropathy, infertility, and hypogonadism with multiple mitochondrial DNA deletions
A Quigley, K Reardon, R Kapsa, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
April 1, 1997
Are mitochondrial DNA deletions causative in chronic progressive external ophthalmoplegia patients?
M J Jean-Francois, S Collins, N Kotsimbos, et al.
Australian and New Zealand Journal of Medicine
|
August 1, 1987
Chronic alcoholic proximal wasting: physiological, morphological and biochemical studies in skeletal muscle
I Trounce, E Byrne, X Dennett, et al.
Journal of Developmental Physiology
|
October 1, 1982
Function of the future respiratory system in the growth retarded fetal sheep
J E Maloney, G Bowes, V Brodecky, 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 deficiencies
E 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 approach
E Byrne, B Jean-Francois, D Thyagarajan, et al.
The Medical Journal of Australia
|
April 16, 1998
Polymyositis caused by a new genus of nematode
X Dennett, S J Siejka, J R Andrews, et al.
Archives of Neurology
|
August 1, 1986
Proximal motor neuropathy, dermato-endocrine syndrome, and IgG kappa paraproteinemia
S F Berkovic, J D Scarlett, G R Symington, et al.
Journal of the Neurological Sciences
|
March 1, 1991
Functional respiratory chain studies in subjects with chronic progressive external ophthalmoplegia and large heteroplasmic mitochondrial DNA deletions
I Trounce, E Byrne, S Marzuki, et al.
Neurology
|
April 24, 1999
Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder
D M Kirby, M Crawford, M A Cleary, et al.
Page
of 6