1. S. Srivastava, F. Diaz, L. Iommarini, K. Aure, A. Lombes, and C. T. Moraes. PGC-1alpha/beta induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders. Hum Mol Genet, 18(10):1805-12, 2009. Note: CA085700/CA/NCI NIH HHS/United StatesEY10804/EY/NEI NIH HHS/United StatesNS041777/NS/NINDS NIH HHS/United StatesJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tEngland. [WWW]



2. K. Aure, K. Mamchaoui, P. Frachon, G. S. Butler-Browne, A. Lombes, and V. Mouly. Impact on oxidative phosphorylation of immortalization with the telomerase gene. Neuromuscul Disord, 17(5):368-75, 2007. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglandNmd. [WWW] Keyword(s): Adenosine Triphosphate/metabolism, Adult, Cell Survival, Cells, Cultured, Child, Child, Preschool, Fibroblasts/drug effects/*physiology, Glucose/pharmacology, Humans, Middle Aged, Mitochondrial Myopathies/pathology, *Oxidative Phosphorylation, Skin/pathology, Telomerase/genetics/*metabolism, Time Factors, Transduction, Genetic/methods.



3. K. Aure, H. Ogier de Baulny, P. Laforet, C. Jardel, B. Eymard, and A. Lombes. Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?. Brain, 130(Pt 6):1516-24, 2007. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglanda journal of neurology. [WWW] Keyword(s): Adolescent, Adult, Age of Onset, Child, Child, Preschool, DNA, Mitochondrial/blood/*genetics, Disease Progression, Follow-Up Studies, Gene Deletion, *Gene Rearrangement, Humans, Kearns-Sayer Syndrome/genetics, Middle Aged, Ophthalmoplegia, Chronic Progressive External/*genetics, Prognosis, Retrospective Studies, Risk Factors.



4. K. Aure, H. O. de Baulny, P. Laforet, C. Jardel, B. Eymard, and A. Lombes. Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?. Brain, 130:1516-1524, 2007. Note: Part 6183IATimes Cited:0Cited References Count:34. [WWW] Keyword(s): mitochondrial disease, deletion, kearns-sayre syndrome, cpeo, natural history, mitochondrial-DNA deletions, marrow-pancreas syndrome, external ophthalmoplegia, pearson-syndrome, tissue distribution, muscle-fibers, myopathies, duplications, plus.



5. K. Aure, G. Fayet, J. P. Leroy, E. Lacene, N. B. Romero, and A. Lombes. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation. Brain, 129(Pt 5):1249-59, 2006. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglanda journal of neurology. [WWW] Keyword(s): Adolescent, Adult, Aged, *Apoptosis, Caspase 3, Caspases/metabolism, Cell Nucleus/ultrastructure, Cell Respiration, Child, DNA, Mitochondrial/analysis/genetics, Electron Transport Complex IV/metabolism, Female, Gene Deletion, Humans, In Situ Nick-End Labeling, Infant, MELAS Syndrome/genetics/pathology, Male, Middle Aged, Mitochondria, Muscle/metabolism/*pathology, Mitochondrial Myopathies/genetics/metabolism/*pathology, Muscle Fibers/enzymology, Muscle, Skeletal/ultrastructure, Point Mutation, bcl-2-Associated X Protein/metabolism.



6. K. Aure, J. F. Benoist, H. Ogier de Baulny, N. B. Romero, O. Rigal, and A. Lombes. Progression despite replacement of a myopathic form of coenzyme Q10 defect. Neurology, 63(4):727-9, 2004. Note: Case ReportsJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Benzoquinones/adverse effects/therapeutic use, Carnitine/therapeutic use, Cerebellar Ataxia/*genetics, Cerebellum/pathology, Child, Preschool, Disease Progression, Drug Therapy, Combination, Exercise Tolerance/drug effects/*genetics, Female, Follow-Up Studies, Humans, Lactates/*blood, Magnetic Resonance Imaging, Mitochondria, Muscle/chemistry, Mitochondrial Myopathies/complications/drug therapy/*genetics/metabolism, Muscle, Skeletal/pathology, Treatment Failure, Ubiquinone/*deficiency/pharmacokinetics/therapeutic use, Vomiting/etiology.



7. K. Aure, D. Sternberg, T. Maisonobe, S. Herson, C. Jardel, P. Blondy, A. Lombes, B. Eymard, and P. Laforet. [Myopathy-lipomatosis associated with A8344G mitochondrial DNA mutation]. Rev Neurol (Paris), 159(12):1163-8, 2003. Note: Case ReportsEnglish AbstractJournal ArticleFrance. [WWW] Keyword(s): *Adenine, DNA, Mitochondrial/*genetics, Female, *Guanine, Humans, Lipomatosis/*genetics, Lysine/genetics, Male, Middle Aged, Muscular Diseases/*genetics, Mutation, RNA, Transfer/genetics.

This material is presented to ensure timely dissemination of scholarly and technical work. Copyright and all rights therein are retained by authors or by other copyright holders. All person copying this information are expected to adhere to the terms and constraints invoked by each author's copyright. In most cases, these works may not be reposted without the explicit permission of the copyright holder.

Les documents contenus dans ces répertoires sont rendus disponibles par les auteurs qui y ont contribué en vue d'assurer la diffusion à temps de travaux savants et techniques sur une base non-commerciale. Les droits de copie et autres droits sont gardés par les auteurs et par les détenteurs du copyright, en dépit du fait qu'ils présentent ici leurs travaux sous forme électronique. Les personnes copiant ces informations doivent adhérer aux termes et contraintes couverts par le copyright de chaque auteur. Ces travaux ne peuvent pas être rendus disponibles ailleurs sans la permission explicite du détenteur du copyright.

This document was translated from BibT_EX by bibtex2html