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Archives of Neurology
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August 12, 2009
Human NARP mitochondrial mutation metabolism corrected with alpha-ketoglutarate/aspartate: a potential new therapy
Gianluca Sgarbi, Gabriella A Casalena, Alessandra Baracca, et al.
Plos One
|
July 15, 2020
Open-tES: An open-source stimulator for transcranial electrical stimulation designed for rodent research
Solène Pedron, Stéphanie Dumontoy, Julien Dimauro, et al.
Brain Pathology (Zurich, Switzerland)
|
April 1, 1992
Disorders associated with depletion of mitochondrial DNA
E Ricci, C T Moraes, S Servidei, et al.
Growth Factors (Chur, Switzerland)
|
January 13, 2011
Modulation of the apoptotic pathway in skeletal muscle models: the role of growth hormone
Ivan Dimauro, Fiorenza Magi, Gina La Sala, et al.
Journal of Child Neurology
|
September 17, 1999
A novel mutation in the mitochondrial DNA transfer ribonucleic acidAsp gene in a child with myoclonic epilepsy and psychomotor regression
A Shtilbans, M El-Schahawi, E Malkin, et al.
Biology of the Neonate
|
January 1, 1995
End-tidal carbon monoxide in newborn infants: observations during the 1st week of life
V Balaraman, S Pelke, S DiMauro, et al.
Neurology
|
April 1, 1993
Polyglucosan body disease simulating amyotrophic lateral sclerosis
T D McDonald, P L Faust, C Bruno, et al.
Archives of Neurology
|
March 11, 2009
Muscle phosphoglycerate mutase deficiency revisited
Ali Naini, Antonio Toscano, Olimpia Musumeci, et al.
Neuromuscular Disorders : NMD
|
March 17, 2009
The m.3244G>A mutation in mtDNA is another cause of progressive external ophthalmoplegia
Evangelia Sotiriou, Jorida Coku, Kurenai Tanji, et al.
Physical Review Letters
|
June 1, 2004
Multiphoton double ionization via field-independent resonant excitation
J Rudati, J L Chaloupka, P Agostini, et al.
Page
of 95
Search research articles
Search
Showing results (281-290 of 942) with videos related to
Sort By:
Page
of 95
Archives of Neurology
|
August 12, 2009
Human NARP mitochondrial mutation metabolism corrected with alpha-ketoglutarate/aspartate: a potential new therapy
Gianluca Sgarbi, Gabriella A Casalena, Alessandra Baracca, et al.
Plos One
|
July 15, 2020
Open-tES: An open-source stimulator for transcranial electrical stimulation designed for rodent research
Solène Pedron, Stéphanie Dumontoy, Julien Dimauro, et al.
Brain Pathology (Zurich, Switzerland)
|
April 1, 1992
Disorders associated with depletion of mitochondrial DNA
E Ricci, C T Moraes, S Servidei, et al.
Growth Factors (Chur, Switzerland)
|
January 13, 2011
Modulation of the apoptotic pathway in skeletal muscle models: the role of growth hormone
Ivan Dimauro, Fiorenza Magi, Gina La Sala, et al.
Journal of Child Neurology
|
September 17, 1999
A novel mutation in the mitochondrial DNA transfer ribonucleic acidAsp gene in a child with myoclonic epilepsy and psychomotor regression
A Shtilbans, M El-Schahawi, E Malkin, et al.
Biology of the Neonate
|
January 1, 1995
End-tidal carbon monoxide in newborn infants: observations during the 1st week of life
V Balaraman, S Pelke, S DiMauro, et al.
Neurology
|
April 1, 1993
Polyglucosan body disease simulating amyotrophic lateral sclerosis
T D McDonald, P L Faust, C Bruno, et al.
Archives of Neurology
|
March 11, 2009
Muscle phosphoglycerate mutase deficiency revisited
Ali Naini, Antonio Toscano, Olimpia Musumeci, et al.
Neuromuscular Disorders : NMD
|
March 17, 2009
The m.3244G>A mutation in mtDNA is another cause of progressive external ophthalmoplegia
Evangelia Sotiriou, Jorida Coku, Kurenai Tanji, et al.
Physical Review Letters
|
June 1, 2004
Multiphoton double ionization via field-independent resonant excitation
J Rudati, J L Chaloupka, P Agostini, et al.
Page
of 95