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Neurology
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November 1, 1991
Adult Reye's syndrome: a review with new evidence for a generalized defect in intramitochondrial enzyme processing
R N Van Coster, D C De Vivo, D Blake, et al.
Neurology
|
August 1, 1982
Familial myoadenylate deaminase deficiency and exertional myalgia
J Kelemen, D R Rice, W G Bradley, et al.
Archives of Neurology
|
March 1, 1993
The syndrome of mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes presenting without stroke
R K Mosewich, J R Donat, S DiMauro, et al.
Neurology
|
August 1, 1980
Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency
S DiMauro, J R Mendell, Z Sahenk, et al.
American Journal of Diseases of Children (1960)
|
June 1, 1991
Autosomal recessive lethal infantile cytochrome C oxidase deficiency
G Eshel, E Lahat, K Fried, et al.
Physical Review Letters
|
February 9, 2005
Self-referencing, spectrally, or spatially encoded spectral interferometry for the complete characterization of attosecond electromagnetic pulses
Eric Cormier, Ian A Walmsley, Ellen M Kosik, et al.
Journal of Inherited Metabolic Disease
|
April 8, 2006
Measurement of ATP production in mitochondrial disorders
R K Shepherd, N Checcarelli, A Naini, et al.
Annals of Neurology
|
April 25, 2006
Early-onset familial parkinsonism due to POLG mutations
Guido Davidzon, Paul Greene, Michelangelo Mancuso, et al.
Biology
|
June 2, 2021
Sildenafil Counteracts the In Vitro Activation of CXCL-9, CXCL-10 and CXCL-11/CXCR3 Axis Induced by Reactive Oxygen Species in Scleroderma Fibroblasts
Cristina Antinozzi, Paolo Sgrò, Francesco Marampon, et al.
Hippocampus
|
August 25, 2015
Transient optogenetic inactivation of the medial entorhinal cortex biases the active population of hippocampal neurons
Jon W Rueckemann, Audrey J DiMauro, Lara M Rangel, et al.
Page
of 95
Search research articles
Search
Showing results (431-440 of 942) with videos related to
Sort By:
Page
of 95
Neurology
|
November 1, 1991
Adult Reye's syndrome: a review with new evidence for a generalized defect in intramitochondrial enzyme processing
R N Van Coster, D C De Vivo, D Blake, et al.
Neurology
|
August 1, 1982
Familial myoadenylate deaminase deficiency and exertional myalgia
J Kelemen, D R Rice, W G Bradley, et al.
Archives of Neurology
|
March 1, 1993
The syndrome of mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes presenting without stroke
R K Mosewich, J R Donat, S DiMauro, et al.
Neurology
|
August 1, 1980
Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency
S DiMauro, J R Mendell, Z Sahenk, et al.
American Journal of Diseases of Children (1960)
|
June 1, 1991
Autosomal recessive lethal infantile cytochrome C oxidase deficiency
G Eshel, E Lahat, K Fried, et al.
Physical Review Letters
|
February 9, 2005
Self-referencing, spectrally, or spatially encoded spectral interferometry for the complete characterization of attosecond electromagnetic pulses
Eric Cormier, Ian A Walmsley, Ellen M Kosik, et al.
Journal of Inherited Metabolic Disease
|
April 8, 2006
Measurement of ATP production in mitochondrial disorders
R K Shepherd, N Checcarelli, A Naini, et al.
Annals of Neurology
|
April 25, 2006
Early-onset familial parkinsonism due to POLG mutations
Guido Davidzon, Paul Greene, Michelangelo Mancuso, et al.
Biology
|
June 2, 2021
Sildenafil Counteracts the In Vitro Activation of CXCL-9, CXCL-10 and CXCL-11/CXCR3 Axis Induced by Reactive Oxygen Species in Scleroderma Fibroblasts
Cristina Antinozzi, Paolo Sgrò, Francesco Marampon, et al.
Hippocampus
|
August 25, 2015
Transient optogenetic inactivation of the medial entorhinal cortex biases the active population of hippocampal neurons
Jon W Rueckemann, Audrey J DiMauro, Lara M Rangel, et al.
Page
of 95