Macrophagic myofasciitis lesions assess long-term persistence of vaccine-derived aluminium hydroxide in muscle
Gherardi, R. K., Coquet, M., Cherin, P., Belec, L., Moretto, P., Dreyfus, P. A., Pellissier, J.-F., Chariot, P., Authier, F.-J.
Published in Brain (London, England : 1878) (01.09.2001)
Published in Brain (London, England : 1878) (01.09.2001)
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Diagnostic evaluation of clinically normal subjects with chronic hyperCKemia
Fernandez, C, de Paula, A Maues, Figarella-Branger, D, Krahn, M, Giorgi, R, Chabrol, B, Monfort, M-F, Pouget, J, Pellissier, J-F
Published in Neurology (23.05.2006)
Published in Neurology (23.05.2006)
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The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein
Rouzier, C, Le Guédard-Méreuze, S, Fragaki, K, Serre, V, Miro, J, Tuffery-Giraud, S, Chaussenot, A, Bannwarth, S, Caruba, C, Ostergaard, E, Pellissier, J-F, Richelme, C, Espil, C, Chabrol, B, Paquis-Flucklinger, V
Published in Journal of medical genetics (01.10.2010)
Published in Journal of medical genetics (01.10.2010)
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Macrophagic myofasciitis: an emerging entity
Gherardi, RK, Coquet, M, Chérin, P, Authier, F-J, Laforêt, P, Bélec, L, Figarella-Branger, D, Mussini, J-M, Pellissier, J-F, Fardeau, M
Published in The Lancet (British edition) (01.08.1998)
Published in The Lancet (British edition) (01.08.1998)
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PMP22 overexpression causes dysmyelination in mice
Robaglia‐Schlupp, A., Pizant, J., Norreel, J.‐C., Passage, E., Sabéran‐Djoneidi, D., Ansaldi, J.‐L., Vinay, L., Figarella‐Branger, D., Lévy, N., Clarac, F., Cau, P., Pellissier, J.‐F., Fontés, M.
Published in Brain (London, England : 1878) (01.10.2002)
Published in Brain (London, England : 1878) (01.10.2002)
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Prognostic factors in intracranial ependymomas in children
Figarella-Branger, D, Civatte, M, Bouvier-Labit, C, Gouvernet, J, Gambarelli, D, Gentet, J C, Lena, G, Choux, M, Pellissier, J F
Published in Journal of neurosurgery (01.10.2000)
Published in Journal of neurosurgery (01.10.2000)
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Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease
Fontés, Michel, Passage, Edith, Norreel, Jean Chrétien, Noack-Fraissignes, Pauline, Sanguedolce, Véronique, Pizant, Josette, Thirion, Xavier, Robaglia-Schlupp, Andrée, Pellissier, Jean François
Published in Nature medicine (01.04.2004)
Published in Nature medicine (01.04.2004)
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Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2
Vihola, A, Bassez, G, Meola, G, Zhang, S, Haapasalo, H, Paetau, A, Mancinelli, E, Rouche, A, Hogrel, J Y, Laforêt, P, Maisonobe, T, Pellissier, J F, Krahe, R, Eymard, B, Udd, B
Published in Neurology (10.06.2003)
Published in Neurology (10.06.2003)
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Correlation Between Varying Levels of PMP22 Expression and the Degree of Demyelination and Reduction in Nerve Conduction Velocity in Transgenic Mice
Huxley, C., Passage, E., Robertson, A. M., Youl, B., Huston, S., Manson, A., Sabéran-Djoniedi, D., Figarella-Branger, D., Pellissier, J. F., Thomas, P. K., Fontés, M.
Published in Human molecular genetics (01.03.1998)
Published in Human molecular genetics (01.03.1998)
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Pituicytomas, a mis-diagnosed benign tumor of the neurohypophysis: report of three cases
FIGARELLA-BRANGER, D, DUFOUR, H, FERNANDEZ, C, BOUVIER-LABIT, C, GRISOLI, F, PELLISSIER, J. F
Published in Acta neuropathologica (01.09.2002)
Published in Acta neuropathologica (01.09.2002)
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The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype
Rouzier, Cécile, Bannwarth, Sylvie, Chaussenot, Annabelle, Chevrollier, Arnaud, Verschueren, Annie, Bonello-Palot, Nathalie, Fragaki, Konstantina, Cano, Aline, Pouget, Jean, Pellissier, Jean-François, Procaccio, Vincent, Chabrol, Brigitte, Paquis-Flucklinger, Véronique
Published in Brain (London, England : 1878) (01.01.2012)
Published in Brain (London, England : 1878) (01.01.2012)
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Local expression of monocyte chemoattractant protein-1 (MCP-1) in idiopathic inflammatory myopathies
LIPRANDI, A, BARTOLI, C, FIGARELLA-BRANGER, D, PELLISSIER, J.-F, LEPIDI, H
Published in Acta neuropathologica (01.06.1999)
Published in Acta neuropathologica (01.06.1999)
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Class I MHC detection as a diagnostic tool in noninformative muscle biopsies of patients suffering from dermatomyositis (DM)
Civatte, M., Schleinitz, N., Krammer, P., Fernandez, C., Guis, S., Veit, V., Pouget, J., Harlé, J.-R., Pellissier, J.-F., Figarella-Branger, D.
Published in Neuropathology and applied neurobiology (01.12.2003)
Published in Neuropathology and applied neurobiology (01.12.2003)
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CCR2A and CCR2B, the two isoforms of the monocyte chemoattractant protein-1 receptor are up-regulated and expressed by different cell subsets in idiopathic inflammatory myopathies
BARTOLI, C, CIVATTE, M, PELLISSIER, J. F, FIGARELLA-BRANGER, D
Published in Acta neuropathologica (01.10.2001)
Published in Acta neuropathologica (01.10.2001)
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Gastrointestinal tract symptoms in Maternally Inherited Diabetes and Deafness (MIDD)
Narbonne, H, Paquis-Fluckinger, V, Valero, R, Heyries, L, Pellissier, JF, Vialettes, B
Published in Diabetes & metabolism (01.02.2004)
Published in Diabetes & metabolism (01.02.2004)
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Tau aggregates are abnormally phosphorylated in inclusion body myositis and have an immunoelectrophoretic profile distinct from other tauopathies
Maurage, C.-A., Bussière, T., Sergeant, N., Ghesteem, A., Figarella-Branger, D., Ruchoux, M.-M., Pellissier, J.-F., Delacourte, A.
Published in Neuropathology and applied neurobiology (01.12.2004)
Published in Neuropathology and applied neurobiology (01.12.2004)
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In vivo and in vitro characterization of skeletal muscle metabolism in patients with statin‐induced adverse effects
Guis, S., Figarella‐branger, D., Mattei, J. P., Nicoli, F., Le Fur, Y., Kozak‐Ribbens, G., Pellissier, J. F., Cozzone, P. J., Amabile, N., Bendahan, D.
Published in Arthritis and rheumatism (15.08.2006)
Published in Arthritis and rheumatism (15.08.2006)
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