Depletion of mitochondrial DNA associated with infantile cholestasis and progressive liver fibrosis by Ducluzeau, Pierre-Henri, Lachaux, Alain, Bouvier, Raymonde, Streichenberger, Nathalie, Stepien, Georges, Mousson, Bénédicte

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Ataxie cérébelleuse récessive par mutation de POLG1 : à propos d’une famille by Kremer, Laurent, Lagha-Boukbiza, Ouhaid, Fleury, Marie-Celine, Lannes, Beatrice, Echaniz-Laguna, Andoni, Mousson De Camaret, Benedicte, Tranchant, Christine

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Identification of a large-scale mitochondrial deoxyribonucleic acid deletion in endocrinopathies and deafness : Report of two unrelated cases with diabetes mellitus and adrenal ins... by NICOLINO, M, FERLIN, T, FOREST, M, GODINOT, C, CARRIER, H, DAVID, M, CHATELAIN, P, MOUSSON, B

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Segregation of the G8993 mutant mitochondrial DNA through generations and embryonic tissues in a family at risk of leigh syndrome by Ferlin, Thérèse, Landrieu, Pierre, Rambaud, Caroline, Fernandez, Hervé, Dumoulin, Renée, Rustin, Pierre, Mousson, Bénédicte

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Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts by Procaccio, V, Mousson, B, Beugnot, R, Duborjal, H, Feillet, F, Putet, G, Pignot-Paintrand, I, Lombès, A, De Coo, R, Smeets, H, Lunardi, J, Issartel, J P

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Quantification of OXPHOS Gene Transcripts during Muscle Cell Differentiation in Patients with Mitochondrial Myopathies by Bonod-Bidaud, Christelle, Giraud, Stéphane, Mandon, Ginette, Mousson, Bénédicte, Stepien, Georges

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Metabolic studies in a patient with severe carnitine palmitoyltransferase type II deficiency by Fontaine, Monique, Briand, Gilbert, Largillière, Claude, Degand, Pierre, Divry, Priscille, Vianey-Saban, Christine, Mousson, Bénédicte, Vamecq, Joseph

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Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial complex I: genomic organization and expression by Procaccio, V, Lescuyer, P, Bourges, I, Beugnot, R, Duborjal, H, Depetris, D, Mousson, B, Montfort, M F, Smeets, H, De Coo, R, Issartel, J P

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Identification of a Large-Scale Mitochondrial Deoxyribonucleic Acid Deletion in Endocrinopathies and Deafness: Report of Two Unrelated Cases with Diabetes Mellitus and Adrenal Insu... by Nicolino, Marc, Ferlin, Thérèse, Forest, Maguelone, Godinot, Catherine, Carrier, Henri, David, Michel, Chatelain, Pierre, Mousson, Bénédicte

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Identification of a Large-Scale Mitochondrial Deoxyribonucleic Acid Deletion in Endocrinopathies and Deafness: Report of Two Unrelated Cases with Diabetes Mellitus and Adrenal Insu... by Nicolino, Marc, Ferlin, Thérèse, Forest, Maguelone, Godinot, Catherine, Carrier, Henri, David, Michel, Chatelain, Pierre, Mousson, Bénédicte

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Necrotizing encephalopathy and macrocephaly with mitochondrial complex I deficiency by Feillet, François, Mousson, Bénédicte, Grignon, Yves, Leonard, James V, Vidailhet, Michel

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Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: expression of the molecular phenotype in cultured muscle cells by Villard, Jean, Fischer, Andréas, Mandon, Ginette, Collombet, Jean Marc, Taroni, Franco, Mousson, Bénédicte

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Molecular histology of mitochondrial and nuclear transcripts in the muscle of patients harbouring a single mitochondrial DNA deletion by CARRIER, H, BURT-PICHAT, B, FLOCARD, F, GUFFON, N, MOUSSON, B, DUMOULIN, R, GODINOT, C

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Progressive reversion of clinical and molecular phenotype in a child with liver mitochondrial DNA depletion by Ducluzeau, Pierre-Henri, Lachaux, Alain, Bouvier, Raymonde, Duborjal, Hervé, Stepien, Georges, Bozon, Dominique, Mousson de Camaret, Bénédicte

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Induction of ANT2 gene expression in liver of patients with mitochondrial DNA depletion by Bonod-Bidaud, Christelle, Chevrollier, Arnaud, Bourasseau, Ingrid, Lachaux, Alain, Mousson de Camaret, Bénédicte, Stepien, Georges

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Drug-resistant cytomegalovirus in transplant recipients: a French cohort study by Hantz, Sébastien, Garnier-Geoffroy, Françoise, Mazeron, Marie-Christine, Garrigue, Isabelle, Merville, Pierre, Mengelle, Catherine, Rostaing, Lionel, Saint Marcoux, Franck, Essig, Marie, Rerolle, Jean-Philippe, Cotin, Sébastien, Germi, Raphaëlle, Pillet, Sylvie, Lebranchu, Yvon, Turlure, Pascal, Alain, Sophie

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SP830EARLY RECURRENCE OF ISOLATED RENAL MICROPOLYANGIITIS DURING THE FIRST THREE MONTHS OF KIDNEY TRANSPLANTATION by Mousson, Christiane I, Tinel, Claire, Kamar, Nassim, del Bello, Arnaud, Laurent, Charlotte, Janbon, Benedicte

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