Clinical features and neuroradiological findings of mitochondrial pathology in six neonates
GIRE, C, GIRARD, N, NICAISE, C, EINAUDI, M. A, MONTFORT, M. F, DEJODE, J. M
Published in Child's nervous system (01.11.2002)
Published in Child's nervous system (01.11.2002)
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Phenotypic expression of diabetes secondary to a T14709C mutation of mitochondrial DNA. Comparison with MIDD syndrome (A3243G mutation): a case report
Vialettes, B H, Paquis-Flucklinger, V, Pelissier, J F, Bendahan, D, Narbonne, H, Silvestre-Aillaud, P, Montfort, M F, Righini-Chossegros, M, Pouget, J, Cozzone, P J, Desnuelle, C
Published in Diabetes care (01.11.1997)
Published in Diabetes care (01.11.1997)
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Stüve-Wiedemann syndrome and defects of the mitochondrial respiratory chain
Chabrol, B, Sigaudy, S, Paquis, V, Montfort, M F, Giudicelli, H, Pellissier, J F, Millet, V, Mancini, J, Philip, N
Published in American journal of medical genetics (17.10.1997)
Published in American journal of medical genetics (17.10.1997)
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Cytochrome c oxydase-deficient Leigh syndrome with homozygous mutation in SURF1 gene
Monnot, S, Chabrol, B, Cano, A, Pellissier, J F, Collignon, P, Montfort, M F, Paquis-Flucklinger, V
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.05.2005)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.05.2005)
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Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial complex I: genomic organization and expression
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
Published in Mammalian genome (01.09.2000)
Published in Mammalian genome (01.09.2000)
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Thyroglobulins of cyclostomes and an elasmobranch
Suzuki, Shintaro, Gorbman, Aubrey, Rolland, Marcel, Montfort, Marie-France, Lissitzky, Serge
Published in General and comparative endocrinology (01.05.1975)
Published in General and comparative endocrinology (01.05.1975)
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Syndrome de Leigh avec déficit en cytochrome c oxydase lié à une mutation homozygote du gène SURF1
Monnot, S., Chabrol, B., Cano, A., Pellissier, J.F., Collignon, P., Montfort, M.F., Paquis-Flucklinger, V.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.05.2005)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.05.2005)
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Efficiency of thyroglobulin as a thyroid hormone-forming protein
Rolland, Marcel, Montfort, Marie-France, Lissitzky, Serge
Published in Biochimica et biophysica acta (20.04.1973)
Published in Biochimica et biophysica acta (20.04.1973)
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Inappropriate liver transplantation in a child with Alpers-Huttenlocher syndrome misdiagnosed as valproate-induced acute liver failure
Delarue, A., Paut, O., Guys, J. -M., Montfort, M. -F., Lethel, V., Roquelaure, B., Pellissier, J. -F., Sarles, J., Camboulives, J.
Published in Pediatric Transplantation (01.02.2000)
Published in Pediatric Transplantation (01.02.2000)
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