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Brain : a Journal of Neurology
|
April 20, 2010
Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes
Charalampos Tzoulis, Gesche Neckelmann, Sverre J Mørk, et al.
Journal of Neuro-Oncology
|
August 4, 2005
Instability of mitochondrial DNA and MRI and clinical correlations in malignant gliomas
Luisa Montanini, Caroline Regna-Gladin, Marica Eoli, et al.
Molecular Genetics and Metabolism
|
December 3, 2019
Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement
Margherita Protasoni, Claudio Bruno, Maria Alice Donati, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 29, 2015
Foxg1 localizes to mitochondria and coordinates cell differentiation and bioenergetics
Laura Pancrazi, Giulietta Di Benedetto, Laura Colombaioni, et al.
International Journal of Molecular Sciences
|
March 10, 2018
Unravelling the Effects of the Mutation m.3571insC/MT-ND1 on Respiratory Complexes Structural Organization
Luisa Iommarini, Anna Ghelli, Concetta Valentina Tropeano, et al.
European Journal of Human Genetics : EJHG
|
February 19, 2009
A novel mutation in the mitochondrial tRNA(Pro) gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency
Paola Da Pozzo, Elena Cardaioli, Edoardo Malfatti, et al.
Human Molecular Genetics
|
February 5, 2003
Constitutive knockout of Surf1 is associated with high embryonic lethality, mitochondrial disease and cytochrome c oxidase deficiency in mice
Alessandro Agostino, Federica Invernizzi, Cecilia Tiveron, et al.
The Journal of Biological Chemistry
|
February 16, 2006
Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex I
Arcangela Iuso, Salvatore Scacco, Claudia Piccoli, et al.
Brain : a Journal of Neurology
|
June 24, 2021
Myopathic mitochondrial DNA depletion syndrome associated with biallelic variants in LIG3
Federica Invernizzi, Andrea Legati, Alessia Nasca, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 3, 2014
A family with paroxysmal nonkinesigenic dyskinesias (PNKD): evidence of mitochondrial dysfunction
Daniele Ghezzi, Carlotta Canavese, Gordana Kovacevic, et al.
Page
of 29
Search research articles
Search
Showing results (131-140 of 289) with videos related to
Sort By:
Page
of 29
Brain : a Journal of Neurology
|
April 20, 2010
Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes
Charalampos Tzoulis, Gesche Neckelmann, Sverre J Mørk, et al.
Journal of Neuro-Oncology
|
August 4, 2005
Instability of mitochondrial DNA and MRI and clinical correlations in malignant gliomas
Luisa Montanini, Caroline Regna-Gladin, Marica Eoli, et al.
Molecular Genetics and Metabolism
|
December 3, 2019
Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement
Margherita Protasoni, Claudio Bruno, Maria Alice Donati, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 29, 2015
Foxg1 localizes to mitochondria and coordinates cell differentiation and bioenergetics
Laura Pancrazi, Giulietta Di Benedetto, Laura Colombaioni, et al.
International Journal of Molecular Sciences
|
March 10, 2018
Unravelling the Effects of the Mutation m.3571insC/MT-ND1 on Respiratory Complexes Structural Organization
Luisa Iommarini, Anna Ghelli, Concetta Valentina Tropeano, et al.
European Journal of Human Genetics : EJHG
|
February 19, 2009
A novel mutation in the mitochondrial tRNA(Pro) gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency
Paola Da Pozzo, Elena Cardaioli, Edoardo Malfatti, et al.
Human Molecular Genetics
|
February 5, 2003
Constitutive knockout of Surf1 is associated with high embryonic lethality, mitochondrial disease and cytochrome c oxidase deficiency in mice
Alessandro Agostino, Federica Invernizzi, Cecilia Tiveron, et al.
The Journal of Biological Chemistry
|
February 16, 2006
Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex I
Arcangela Iuso, Salvatore Scacco, Claudia Piccoli, et al.
Brain : a Journal of Neurology
|
June 24, 2021
Myopathic mitochondrial DNA depletion syndrome associated with biallelic variants in LIG3
Federica Invernizzi, Andrea Legati, Alessia Nasca, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 3, 2014
A family with paroxysmal nonkinesigenic dyskinesias (PNKD): evidence of mitochondrial dysfunction
Daniele Ghezzi, Carlotta Canavese, Gordana Kovacevic, et al.
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of 29