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The New England Journal of Medicine
|
May 18, 1989
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
C T Moraes, S DiMauro, M Zeviani, et al.
Acta Neuropathologica
|
December 10, 2002
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction
Kurenai Tanji, Josep Gamez, Carles Cervera, et al.
Annals of Neurology
|
June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene
A L Andreu, K Tanji, C Bruno, et al.
Science (New York, N.Y.)
|
August 11, 2000
High-gain harmonic-generation free-electron laser
Yu, Babzien, Ben-Zvi, et al.
Anales Espanoles De Pediatria
|
February 1, 1991
[Clinical and biochemical heterogeneity of childhood cytochrome C deficiency. Review of the literature]
M Roig Quilis, J Sánchez Esteban, A Lombes, et al.
Plos One
|
July 24, 2014
Platelet-rich plasma and skeletal muscle healing: a molecular analysis of the early phases of the regeneration process in an experimental animal model
Ivan Dimauro, Loredana Grasso, Simona Fittipaldi, et al.
Neurology
|
February 1, 1991
Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approach
H J Tritschler, E Bonilla, A Lombes, et al.
Spine
|
September 11, 2025
Microdose Intrathecal Morphine Injection in Teenagers Undergoing Scoliosis Surgery Decreases Length of Stay, Pain Scores, and Opioid Consumption
Vishal Sarwahi, Alexander Morledge, Anabelle Cohen, et al.
Pediatric Research
|
November 14, 1997
Deficient muscle carnitine transport in primary carnitine deficiency
R Pons, R Carrozzo, I Tein, et al.
Genetics, Selection, Evolution : GSE
|
August 14, 2016
Use of canonical discriminant analysis to study signatures of selection in cattle
Silvia Sorbolini, Giustino Gaspa, Roberto Steri, et al.
Page
of 95
Search research articles
Search
Showing results (671-680 of 942) with videos related to
Sort By:
Page
of 95
The New England Journal of Medicine
|
May 18, 1989
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
C T Moraes, S DiMauro, M Zeviani, et al.
Acta Neuropathologica
|
December 10, 2002
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction
Kurenai Tanji, Josep Gamez, Carles Cervera, et al.
Annals of Neurology
|
June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene
A L Andreu, K Tanji, C Bruno, et al.
Science (New York, N.Y.)
|
August 11, 2000
High-gain harmonic-generation free-electron laser
Yu, Babzien, Ben-Zvi, et al.
Anales Espanoles De Pediatria
|
February 1, 1991
[Clinical and biochemical heterogeneity of childhood cytochrome C deficiency. Review of the literature]
M Roig Quilis, J Sánchez Esteban, A Lombes, et al.
Plos One
|
July 24, 2014
Platelet-rich plasma and skeletal muscle healing: a molecular analysis of the early phases of the regeneration process in an experimental animal model
Ivan Dimauro, Loredana Grasso, Simona Fittipaldi, et al.
Neurology
|
February 1, 1991
Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approach
H J Tritschler, E Bonilla, A Lombes, et al.
Spine
|
September 11, 2025
Microdose Intrathecal Morphine Injection in Teenagers Undergoing Scoliosis Surgery Decreases Length of Stay, Pain Scores, and Opioid Consumption
Vishal Sarwahi, Alexander Morledge, Anabelle Cohen, et al.
Pediatric Research
|
November 14, 1997
Deficient muscle carnitine transport in primary carnitine deficiency
R Pons, R Carrozzo, I Tein, et al.
Genetics, Selection, Evolution : GSE
|
August 14, 2016
Use of canonical discriminant analysis to study signatures of selection in cattle
Silvia Sorbolini, Giustino Gaspa, Roberto Steri, et al.
Page
of 95