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The European Journal of Neuroscience
|
July 10, 2020
Chronic fluoxetine or ketamine treatment differentially affects brain energy homeostasis which is not exacerbated in mice with trait suboptimal mitochondrial function
Tim L Emmerzaal, Leah Jacobs, Bram Geenen, et al.
Journal of Inherited Metabolic Disease
|
March 5, 2015
Whole exome sequencing of suspected mitochondrial patients in clinical practice
Saskia B Wortmann, David A Koolen, Jan A Smeitink, et al.
Orphanet Journal of Rare Diseases
|
February 28, 2024
Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethality
Firas Abu Hanna, Yoav Zehavi, Eran Cohen-Barak, et al.
Neuroscience and Biobehavioral Reviews
|
May 17, 2021
Effect of neuropsychiatric medications on mitochondrial function: For better or for worse
Tim L Emmerzaal, Gerben Nijkamp, Marin Veldic, et al.
EMBO Molecular Medicine
|
March 9, 2016
Mitochondrial disorders in children: toward development of small-molecule treatment strategies
Werner Jh Koopman, Julien Beyrath, Cheuk-Wing Fung, et al.
Mitochondrion
|
June 28, 2011
New mitochondrial tRNA HIS mutation in a family with lactic acidosis and stroke-like episodes (MELAS)
Maria Antonietta Calvaruso, Michel A Willemsen, Richard J Rodenburg, et al.
Molecular Genetics and Metabolism Reports
|
July 17, 2018
Effectiveness of whole exome sequencing in unsolved patients with a clinical suspicion of a mitochondrial disorder in Estonia
Sanna Puusepp, Karit Reinson, Sander Pajusalu, et al.
American Journal of Medical Genetics. Part A
|
March 15, 2006
Clinical and biochemical characteristics in patients with a high mutant load of the mitochondrial T8993G/C mutations
Eva Morava, Richard J Rodenburg, Frans Hol, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 18, 2013
A guide to diagnosis and treatment of Leigh syndrome
Fabian Baertling, Richard J Rodenburg, Jörg Schaper, et al.
Journal of Medical Genetics
|
May 28, 2011
Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome
Elsebet Ostergaard, Richard J Rodenburg, Mariël van den Brand, et al.
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of 14
Search research articles
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Showing results (11-20 of 137) with videos related to
Sort By:
Page
of 14
The European Journal of Neuroscience
|
July 10, 2020
Chronic fluoxetine or ketamine treatment differentially affects brain energy homeostasis which is not exacerbated in mice with trait suboptimal mitochondrial function
Tim L Emmerzaal, Leah Jacobs, Bram Geenen, et al.
Journal of Inherited Metabolic Disease
|
March 5, 2015
Whole exome sequencing of suspected mitochondrial patients in clinical practice
Saskia B Wortmann, David A Koolen, Jan A Smeitink, et al.
Orphanet Journal of Rare Diseases
|
February 28, 2024
Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethality
Firas Abu Hanna, Yoav Zehavi, Eran Cohen-Barak, et al.
Neuroscience and Biobehavioral Reviews
|
May 17, 2021
Effect of neuropsychiatric medications on mitochondrial function: For better or for worse
Tim L Emmerzaal, Gerben Nijkamp, Marin Veldic, et al.
EMBO Molecular Medicine
|
March 9, 2016
Mitochondrial disorders in children: toward development of small-molecule treatment strategies
Werner Jh Koopman, Julien Beyrath, Cheuk-Wing Fung, et al.
Mitochondrion
|
June 28, 2011
New mitochondrial tRNA HIS mutation in a family with lactic acidosis and stroke-like episodes (MELAS)
Maria Antonietta Calvaruso, Michel A Willemsen, Richard J Rodenburg, et al.
Molecular Genetics and Metabolism Reports
|
July 17, 2018
Effectiveness of whole exome sequencing in unsolved patients with a clinical suspicion of a mitochondrial disorder in Estonia
Sanna Puusepp, Karit Reinson, Sander Pajusalu, et al.
American Journal of Medical Genetics. Part A
|
March 15, 2006
Clinical and biochemical characteristics in patients with a high mutant load of the mitochondrial T8993G/C mutations
Eva Morava, Richard J Rodenburg, Frans Hol, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 18, 2013
A guide to diagnosis and treatment of Leigh syndrome
Fabian Baertling, Richard J Rodenburg, Jörg Schaper, et al.
Journal of Medical Genetics
|
May 28, 2011
Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome
Elsebet Ostergaard, Richard J Rodenburg, Mariël van den Brand, et al.
Page
of 14