Search research articles
Contact Us
Filters
Showing results (221-230 of 1,071) with videos related to
Page
of 108
Sort By:
Human Mutation
|
January 1, 1994
An A-to-C substitution involving the translation initiation codon in a patient with myophosphorylase deficiency (McArdle's disease)
S Tsujino, L A Rubin, S Shanske, et al.
BMC Research Notes
|
September 22, 2012
A simple protocol for the subcellular fractionation of skeletal muscle cells and tissue
Ivan Dimauro, Timothy Pearson, Daniela Caporossi, et al.
Archives of Neurology
|
November 10, 2004
A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism
Michelangelo Mancuso, Massimiliano Filosto, Shin J Oh, et al.
Epilepsy Research. Supplement
|
January 1, 1991
Epilepsy in mitochondrial encephalomyopathies
S DiMauro, E Ricci, M Hirano, et al.
Behaviour Research and Therapy
|
December 25, 2012
Long-term effectiveness of CBT for anxiety disorders in an adult outpatient clinic sample: a follow-up study
Jennifer DiMauro, Janine Domingues, Geraldine Fernandez, et al.
Sensors (Basel, Switzerland)
|
June 24, 2022
Industry 4.0 and Precision Livestock Farming (PLF): An up to Date Overview across Animal Productions
Sarah Morrone, Corrado Dimauro, Filippo Gambella, et al.
The Journal of Pediatrics
|
July 1, 1988
Fatal infantile cardiopathy caused by phosphorylase b kinase deficiency
S Servidei, L A Metlay, J Chodosh, et al.
Neurologic Clinics
|
February 1, 1989
Mitochondrial diseases
M Zeviani, E Bonilla, D C DeVivo, et al.
Free Radical Biology & Medicine
|
October 2, 2012
In vitro susceptibility of thioredoxins and glutathione to redox modification and aging-related changes in skeletal muscle
Ivan Dimauro, Timothy Pearson, Daniela Caporossi, et al.
Journal of Molecular Biology
|
February 20, 1989
Q beta replicase: mapping the functional domains of an RNA-dependent RNA polymerase
D R Mills, C Priano, P DiMauro, et al.
Page
of 108
Search research articles
Search
Showing results (221-230 of 1,071) with videos related to
Sort By:
Page
of 108
Human Mutation
|
January 1, 1994
An A-to-C substitution involving the translation initiation codon in a patient with myophosphorylase deficiency (McArdle's disease)
S Tsujino, L A Rubin, S Shanske, et al.
BMC Research Notes
|
September 22, 2012
A simple protocol for the subcellular fractionation of skeletal muscle cells and tissue
Ivan Dimauro, Timothy Pearson, Daniela Caporossi, et al.
Archives of Neurology
|
November 10, 2004
A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism
Michelangelo Mancuso, Massimiliano Filosto, Shin J Oh, et al.
Epilepsy Research. Supplement
|
January 1, 1991
Epilepsy in mitochondrial encephalomyopathies
S DiMauro, E Ricci, M Hirano, et al.
Behaviour Research and Therapy
|
December 25, 2012
Long-term effectiveness of CBT for anxiety disorders in an adult outpatient clinic sample: a follow-up study
Jennifer DiMauro, Janine Domingues, Geraldine Fernandez, et al.
Sensors (Basel, Switzerland)
|
June 24, 2022
Industry 4.0 and Precision Livestock Farming (PLF): An up to Date Overview across Animal Productions
Sarah Morrone, Corrado Dimauro, Filippo Gambella, et al.
The Journal of Pediatrics
|
July 1, 1988
Fatal infantile cardiopathy caused by phosphorylase b kinase deficiency
S Servidei, L A Metlay, J Chodosh, et al.
Neurologic Clinics
|
February 1, 1989
Mitochondrial diseases
M Zeviani, E Bonilla, D C DeVivo, et al.
Free Radical Biology & Medicine
|
October 2, 2012
In vitro susceptibility of thioredoxins and glutathione to redox modification and aging-related changes in skeletal muscle
Ivan Dimauro, Timothy Pearson, Daniela Caporossi, et al.
Journal of Molecular Biology
|
February 20, 1989
Q beta replicase: mapping the functional domains of an RNA-dependent RNA polymerase
D R Mills, C Priano, P DiMauro, et al.
Page
of 108