1. A. Amiot, M. Tchikviladze, F. Joly, A. Slama, D. C. Hatem, C. Jardel, B. Messing, and A. Lombes. Frequency of mitochondrial defects in patients with chronic intestinal pseudo-obstruction. Gastroenterology, 137(1):101-9, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]



2. M. O. Habert, L. C. de Souza, F. Lamari, N. Daragon, S. Desarnaud, C. Jardel, B. Dubois, and M. Sarazin. Brain perfusion SPECT correlates with CSF biomarkers in Alzheimer's disease. Eur J Nucl Med Mol Imaging, 2009. Note: Journal article. [WWW]



3. E. Maillart, C. Acquaviva-Bourdain, O. Rigal, M. Brivet, C. Jardel, A. Lombes, B. Eymard, C. Vianey-Saban, and P. Laforet. [Multiple acyl-CoA dehydrogenase deficiency (MADD): A curable cause of genetic muscular lipidosis.]. Rev Neurol (Paris), 2009. Note: Journal article. [WWW]



4. F. Medja, S. Allouche, P. Frachon, C. Jardel, M. Malgat, B. M. de Camaret, A. Slama, J. Lunardi, J. P. Mazat, and A. Lombes. Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis. Mitochondrion, 9(5):331-9, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tNetherlands. [WWW]



5. S. Mercier, M. Josselin de Wasch, F. Labarthe, C. Jardel, A. Lombes, A. Munnich, A. Toutain, H. Nivet, E. Saliba, A. Chantepie, and P. Castelnau. [Clinical variability and diagnosis steps in childhood mitochondrial disease]. Arch Pediatr, 16(4):322-30, 2009. Note: English AbstractJournal ArticleFranceorgane officiel de la Societe francaise de pediatrie. [WWW] Keyword(s): Adolescent, Age of Onset, Central Nervous System Diseases/etiology, Child, Child, Preschool, Female, Growth Disorders/etiology, Heart Diseases/etiology, Humans, Infant, Infant, Newborn, Male, Mitochondrial Diseases/classification/*diagnosis/epidemiology, Muscle Hypotonia/etiology, Retrospective Studies.



6. J. Poulton, M. Hirano, A. Spinazzola, M. Arenas Hernandez, C. Jardel, A. Lombes, B. Czermin, R. Horvath, J. W. Taanman, A. Rotig, M. Zeviani, and C. Fratter. Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1). Biochim Biophys Acta, 2009. Note: Journal article. [WWW]



7. M. Tateo, A. M. Roque-Afonso, T. M. Antonini, F. Medja, A. Lombes, C. Jardel, E. Teicher, M. Sebagh, B. Roche, D. Castaing, D. Samuel, and J. C. Duclos-Vallee. Long-term follow-up of liver transplanted HIV/hepatitis B virus coinfected patients: perfect control of hepatitis B virus replication and absence of mitochondrial toxicity. Aids, 23(9):1069-76, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Adult, Antiretroviral Therapy, Highly Active/*adverse effects, Female, Follow-Up Studies, Graft Survival, HIV/physiology, HIV Infections/*complications/mortality/virology, Hepatitis B virus/physiology, Hepatitis B, Chronic/*complications/prevention & control, Hepatitis C, Chronic/complications, Hepatitis D, Chronic/complications, Humans, Immunosuppressive Agents/therapeutic use, Liver Failure/mortality/*surgery/virology, *Liver Transplantation/mortality, Male, Middle Aged, Mitochondrial Diseases/*chemically induced, Prospective Studies, Recurrence/prevention & control, Survival Rate, Treatment Outcome, Virus Replication.



8. M. J. Kim, C. Jardel, C. Barthelemy, V. Jan, J. P. Bastard, S. Fillaut-Chapin, S. Houry, J. Capeau, and A. Lombes. Mitochondrial DNA content, an inaccurate biomarker of mitochondrial alteration in human immunodeficiency virus-related lipodystrophy. Antimicrob Agents Chemother, 52(5):1670-6, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]



9. 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.



10. 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.



11. I. Le Ber, O. Dubourg, J. F. Benoist, C. Jardel, F. Mochel, M. Koenig, A. Brice, A. Lombes, and A. Durr. Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1. Neurology, 68(4):295-297, 2007. [WWW]



12. R. Ben Yaou, P. Laforet, H. M. Becane, C. Jardel, D. Sternberg, A. Lombes, and B. Eymard. [Misdiagnosis of mitochondrial myopathies: a study of 12 thymectomized patients]. Rev Neurol (Paris), 162(3):339-46, 2006. Note: Case ReportsEnglish AbstractJournal ArticleResearch Support, Non-U.S. Gov'tFrance. [WWW] Keyword(s): Administration, Oral, Adolescent, Adult, Aged, Blepharoptosis/etiology, Cardiomyopathies/etiology, Child, Child, Preschool, Cholinesterase Inhibitors/administration & dosage/diagnostic use, DNA, Mitochondrial/genetics, *Diagnostic Errors, Disease Progression, Electromyography, Electron Transport Complex IV/analysis, Female, Hearing Loss, Sensorineural/etiology, Humans, Injections, Male, Middle Aged, Mitochondrial Myopathies/complications/*diagnosis/genetics/pathology, Muscle Fatigue, Muscle Fibers/enzymology/ultrastructure, Myasthenia Gravis/*diagnosis, Neurologic Examination, Ocular Motility Disorders/etiology, Retrospective Studies, *Thymectomy, *Unnecessary Procedures.



13. M. Laloi-Michelin, M. Virally, C. Jardel, T. Meas, I. Ingster-Moati, A. Lombes, P. Massin, H. Chabriat, A. Tielmans, J. Mikol, and P. J. Guillausseau. Kearns Sayre syndrome: an unusual form of mitochondrial diabetes. Diabetes Metab, 32(2):182-6, 2006. Note: Case ReportsJournal ArticleFrance. [WWW] Keyword(s): Biopsy, Diabetes Mellitus/*diagnosis, Diabetes, Gestational/drug therapy, Female, Humans, Insulin/therapeutic use, Kearns-Sayer Syndrome/*etiology/pathology, Middle Aged, Muscle, Skeletal/pathology, Pregnancy.



14. J. C. Duclos-Vallee, D. Vittecoq, E. Teicher, C. Feray, A. M. Roque-Afonso, A. Lombes, C. Jardel, M. Gigou, E. Dussaix, M. Sebagh, C. Guettier, D. Azoulay, R. Adam, P. Ichai, F. Saliba, B. Roche, D. Castaing, H. Bismuth, and D. Samuel. Hepatitis C virus viral recurrence and liver mitochondrial damage after liver transplantation in HIV-HCV co-infected patients. J Hepatol, 42(3):341-9, 2005. Note: Journal ArticleEngland. [WWW] Keyword(s): Adult, Antiretroviral Therapy, Highly Active, Antiviral Agents/therapeutic use, Bilirubin/blood, Chronic Disease, Female, France, HIV Infections/*complications, Hepatitis C/blood/complications/*pathology/*surgery, Hepatitis C, Chronic/blood/complications/pathology/surgery, Humans, Immunosuppression/methods, Liver Transplantation/immunology/*pathology, Male, Middle Aged, Mitochondria, Liver/*pathology/virology, RNA, Viral/blood, Recurrence, Retrospective Studies, Treatment Outcome, Viral Load.



15. J. Ghosn, M. Guiguet, C. Jardel, R. Benyaou, V. Zeller, A. Simon, M. A. Valantin, B. Amellal, L. Assoumo, J. Y. Hogrel, D. Costagliola, C. Katlama, and A. Lombes. Muscle and liver lactate metabolism in HAART-treated and naive HIV-infected patients: the MITOVIR study. Antivir Ther, 10(4):543-50, 2005. Note: Comparative StudyJournal ArticleMulticenter StudyResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Adult, Aged, Antiretroviral Therapy, Highly Active/*adverse effects, Cross-Sectional Studies, Female, HIV Infections/*drug therapy, Humans, Lactic Acid/*metabolism, Liver/*drug effects/metabolism, Male, Middle Aged, Muscle, Skeletal/*drug effects/metabolism.



16. F. Labarthe, D. Dobbelaere, L. Devisme, A. De Muret, C. Jardel, J. W. Taanman, F. Gottrand, and A. Lombes. Clinical, biochemical and morphological features of hepatocerebral syndrome with mitochondrial DNA depletion due to deoxyguanosine kinase deficiency. J Hepatol, 43(2):333-41, 2005. Note: Case ReportsJournal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Biopsy, Blotting, Southern, Child, Preschool, DNA, Mitochondrial/*genetics, Disease Progression, Fatal Outcome, Female, Hepatocytes/ultrastructure, *Hepatolenticular Degeneration/genetics/metabolism/pathology, Humans, Infant, Infant, Newborn, Liver Failure/etiology/metabolism/pathology, Male, Microscopy, Electron, Pedigree, Phosphotransferases (Alcohol Group Acceptor)/*deficiency/genetics, Polymerase Chain Reaction, Pregnancy, Prenatal Diagnosis, Syndrome.



17. 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.

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