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Neurology
|
November 13, 2002
Diagnostic criteria for respiratory chain disorders in adults and children
F P Bernier, A Boneh, X Dennett, et al.
Clinical and Experimental Neurology
|
January 1, 1993
Motor nerve biopsy: feasibility and safety
P Gates, E Byrne, P McKelvie, 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) syndrome
E Byrne, I Trounce, S Marzuki, et al.
Clinical and Experimental Neurology
|
January 1, 1992
Hereditary sensory radicular neuropathy: defective neurogenic inflammation
R A Westerman, A Block, A Nunn, et al.
Journal of Child Neurology
|
October 31, 1998
Congenital muscular dystrophy, white-matter abnormalities, and neuronal migration disorders: the expanding concept
M T Mackay, A J Kornberg, L Shield, et al.
The Journal of Pediatrics
|
March 1, 1997
Mitochondrial electron transport chain defect presenting as hypoglycemia
M L Freckmann, D R Thorburn, D M Kirby, et al.
American Journal of Human Genetics
|
September 1, 1992
A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I
P Lertrit, A S Noer, M J Jean-Francois, et al.
Brain : a Journal of Neurology
|
June 1, 1986
Dominantly inherited cardioskeletal myopathy with lysosomal glycogen storage and normal acid maltase levels
E Byrne, X Dennett, B Crotty, et al.
Neurology
|
February 26, 2003
Clinical course correlates poorly with muscle pathology in nemaline myopathy
M M Ryan, B Ilkovski, C D Strickland, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 59) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 59 results.
Neurology
|
November 13, 2002
Diagnostic criteria for respiratory chain disorders in adults and children
F P Bernier, A Boneh, X Dennett, et al.
Clinical and Experimental Neurology
|
January 1, 1993
Motor nerve biopsy: feasibility and safety
P Gates, E Byrne, P McKelvie, 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) syndrome
E Byrne, I Trounce, S Marzuki, et al.
Clinical and Experimental Neurology
|
January 1, 1992
Hereditary sensory radicular neuropathy: defective neurogenic inflammation
R A Westerman, A Block, A Nunn, et al.
Journal of Child Neurology
|
October 31, 1998
Congenital muscular dystrophy, white-matter abnormalities, and neuronal migration disorders: the expanding concept
M T Mackay, A J Kornberg, L Shield, et al.
The Journal of Pediatrics
|
March 1, 1997
Mitochondrial electron transport chain defect presenting as hypoglycemia
M L Freckmann, D R Thorburn, D M Kirby, et al.
American Journal of Human Genetics
|
September 1, 1992
A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I
P Lertrit, A S Noer, M J Jean-Francois, et al.
Brain : a Journal of Neurology
|
June 1, 1986
Dominantly inherited cardioskeletal myopathy with lysosomal glycogen storage and normal acid maltase levels
E Byrne, X Dennett, B Crotty, et al.
Neurology
|
February 26, 2003
Clinical course correlates poorly with muscle pathology in nemaline myopathy
M M Ryan, B Ilkovski, C D Strickland, et al.
Page
of 6