Search Results - "Authier, Francois Jerome"

Myalgia and chronic fatigue syndrome following immunization: macrophagic myofasciitis and animal studies support linkage to aluminum adjuvant persistency and diffusion in the immune system by Gherardi, Romain K., Crépeaux, Guillemette, Authier, François-Jérome

“…Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a multifactorial and poorly undersood disabling disease. We present epidemiological, clinical…”
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Necroptosis mediates myofibre death in dystrophin-deficient mice by Morgan, Jennifer E., Prola, Alexandre, Mariot, Virginie, Pini, Veronica, Meng, Jinhong, Hourde, Christophe, Dumonceaux, Julie, Conti, Francesco, Relaix, Frederic, Authier, Francois-Jerôme, Tiret, Laurent, Muntoni, Francesco, Bencze, Maximilien

“…Duchenne muscular dystrophy (DMD) is a severe degenerative disorder caused by mutations in the dystrophin gene. Dystrophin-deficient muscles are characterised…”
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Idiopathic eosinophilic myositis: a systematic literature review by Fermon, Cécile, Authier, François-Jérôme, Gallay, Laure

“…•Eosinophilic myositis are defined by a muscle eosinophilic infiltrate.•Eosinophilic myositis are divided in subtypes according to the histological…”
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JAK inhibitors are effective in a subset of patients with juvenile dermatomyositis: a monocentric retrospective study by Le Voyer, Tom, Gitiaux, Cyril, Authier, François-Jérôme, Bodemer, Christine, Melki, Isabelle, Quartier, Pierre, Aeschlimann, Florence, Isapof, Arnaud, Herbeuval, Jean Philippe, Bondet, Vincent, Charuel, Jean-Luc, Frémond, Marie-Louise, Duffy, Darragh, Rodero, Mathieu P, Bader-Meunier, Brigitte

“…Abstract Objective To evaluate the efficacy and safety of Janus kinase inhibitors (JAKis) in JDM. Methods We conducted a single-centre retrospective study of…”
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Muscle ischaemia associated with NXP2 autoantibodies: a severe subtype of juvenile dermatomyositis by Aouizerate, Jessie, De Antonio, Marie, Bader-Meunier, Brigitte, Barnerias, Christine, Bodemer, Christine, Isapof, Arnaud, Quartier, Pierre, Melki, Isabelle, Charuel, Jean-Luc, Bassez, Guillaume, Desguerre, Isabelle, Gherardi, Romain K, Authier, François-Jérôme, Gitiaux, Cyril

“…Abstract Objectives Myositis-specific autoantibodies (MSAs) are increasingly used to delineate distinct subgroups of JDM. The aim of our study was to explore…”
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Muscle satellite cells and endothelial cells: close neighbors and privileged partners by Christov, Christo, Chrétien, Fabrice, Abou-Khalil, Rana, Bassez, Guillaume, Vallet, Grégoire, Authier, François-Jérôme, Bassaglia, Yann, Shinin, Vasily, Tajbakhsh, Shahragim, Chazaud, Bénédicte, Gherardi, Romain K

“…Genetically engineered mice (Myf5nLacZ/+, Myf5GFP-P/+) allowing direct muscle satellite cell (SC) visualization indicate that, in addition to being located…”
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Critical analysis of reference studies on the toxicokinetics of aluminum-based adjuvants by Masson, Jean-Daniel, Crépeaux, Guillemette, Authier, François-Jérôme, Exley, Christopher, Gherardi, Romain K.

“…We reviewed the three toxicokinetic reference studies commonly used to suggest that aluminum (Al)-based adjuvants are innocuous. A single experimental study…”
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Non-linear dose-response of aluminium hydroxide adjuvant particles: selective low dose neurotoxicity by Crépeaux, Guillemette, Eidi, Housam, David, Marie-Odile, Baba-Amer, Yasmine, Tzavara, Eleni, Giros, Bruno, Authier, François-Jérôme, Exley, Christopher, Shaw, Christopher A, Cadusseau, Josette, Gherardi, Romain K

“…Abstract Aluminium (Al) oxyhydroxide (Alhydrogel® ), the main adjuvant licensed for human and animal vaccines, consists of primary nanoparticles that…”
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Receptor interacting protein kinase‐3 mediates both myopathy and cardiomyopathy in preclinical animal models of Duchenne muscular dystrophy by Bencze, Maximilien, Periou, Baptiste, Punzón, Isabel, Barthélémy, Inès, Taglietti, Valentina, Hou, Cyrielle, Zaidan, Louai, Kefi, Kaouthar, Blot, Stéphane, Agbulut, Onnik, Gervais, Marianne, Derumeaux, Geneviève, Authier, François‐Jérôme, Tiret, Laurent, Relaix, Fréderic

“…Background Duchenne muscular dystrophy (DMD) is a progressive muscle degenerative disorder, culminating in a complete loss of ambulation, hypertrophic…”
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Thyroid-stimulating hormone receptor signaling restores skeletal muscle stem cell regeneration in rats with muscular dystrophy by Taglietti, Valentina, Kefi, Kaouthar, Rivera, Lea, Bergiers, Oriane, Cardone, Nastasia, Coulpier, Fanny, Gioftsidi, Stamatia, Drayton-Libotte, Bernadette, Hou, Cyrielle, Authier, François-Jérôme, Pietri-Rouxel, France, Robert, Matthieu, Bremond-Gignac, Dominique, Bruno, Claudio, Fiorillo, Chiara, Malfatti, Edoardo, Lafuste, Peggy, Tiret, Laurent, Relaix, Frédéric

“…Duchenne muscular dystrophy (DMD) is a severe and progressive myopathy leading to motor and cardiorespiratory impairment. We analyzed samples from patients…”
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Autocrine and Paracrine Angiopoietin 1/Tie-2 Signaling Promotes Muscle Satellite Cell Self-Renewal by Abou-Khalil, Rana, Le Grand, Fabien, Pallafacchina, Giorgia, Valable, Samuel, Authier, François-Jérôme, Rudnicki, Michael A., Gherardi, Romain K., Germain, Stéphane, Chretien, Fabrice, Sotiropoulos, Athanassia, Lafuste, Peggy, Montarras, Didier, Chazaud, Bénédicte

“…Mechanisms governing muscle satellite cell withdrawal from cell cycle to enter into quiescence remain poorly understood. We studied the role of angiopoietin 1…”
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Hemifacial myohyperplasia is due to somatic muscular PIK3CA gain-of-function mutations and responds to pharmacological inhibition by Bayard, Charles, Segna, Eleonora, Taverne, Maxime, Fraissenon, Antoine, Hennocq, Quentin, Periou, Baptiste, Zerbib, Lola, Ladraa, Sophia, Chapelle, Célia, Hoguin, Clément, Kaltenbach, Sophie, Villarese, Patrick, Asnafi, Vahid, Broissand, Christine, Nemazanyy, Ivan, Autret, Gwennhael, Goudin, Nicolas, Legendre, Christophe, Authier, François-Jérôme, Viel, Thomas, Tavitian, Bertrand, Gitiaux, Cyril, Fraitag, Sylvie, Duong, Jean-Paul, Delcros, Clarisse, Sergent, Bernard, Picard, Arnaud, Dussiot, Michael, Guibaud, Laurent, Khonsari, Roman, Canaud, Guillaume

“…Hemifacial myohyperplasia (HFMH) is a rare cause of facial asymmetry exclusively involving facial muscles. The underlying cause and the mechanism of disease…”
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Clinical impact of dual-tracer FDOPA and FDG PET/CT for the evaluation of patients with parkinsonian syndromes by Emsen, Berivan, Villafane, Gabriel, David, Jean-Philippe, Evangelista, Eva, Chalaye, Julia, Lerman, Lionel, Authier, François-Jérôme, Gracies, Jean-Michel, Itti, Emmanuel

“…Parkinsonian syndromes include typical cases of idiopathic Parkinson's disease (PD) and atypical parkinsonian syndromes (APS) associated with cognitive and…”
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Anti-SAE autoantibody in dermatomyositis: original comparative study and review of the literature by Demortier, Juliette, Vautier, Mathieu, Chosidow, Olivier, Gallay, Laure, Bessis, Didier, Berezne, Alice, Cordel, Nadège, Schmidt, Jean, Smail, Amar, Duffau, Pierre, Jachiet, Marie, Begon, Edouard, Gottlieb, Jeremy, Chasset, François, Graveleau, Julie, Marque, Myriam, Cesbron, Elise, Forestier, Amandine, Josse, Séverine, Kluger, Nicolas, Beauchêne, Caroline, Le Corre, Yannick, Pagis, Valentine, Rigolet, Aude, Guillaume-Jugnot, Perrine, Authier, François-Jérôme, Guilain, Nelly, Streichenberger, Nathalie, Leonard-Louis, Sarah, Boussouar, Samia, Landon-Cardinal, Océane, Benveniste, Olivier, Allenbach, Yves

“…Abstract Objective Among specific autoantibodies in DM, the anti–small ubiquitin-like modifier activating enzyme (SAE) antibody is rare. We aim to describe the…”
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Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling by Schuermans, Nika, El Chehadeh, Salima, Hemelsoet, Dimitri, Gautheron, Jérémie, Vantyghem, Marie-Christine, Nouioua, Sonia, Tazir, Meriem, Vigouroux, Corinne, Auclair, Martine, Bogaert, Elke, Dufour, Sara, Okawa, Fumiya, Hilbert, Pascale, Van Doninck, Nike, Taquet, Marie-Caroline, Rosseel, Toon, De Clercq, Griet, Debackere, Elke, Van Haverbeke, Carole, Cherif, Ferroudja Ramdane, Urtizberea, Jon Andoni, Chanson, Jean-Baptiste, Funalot, Benoit, Authier, François-Jérôme, Kaya, Sabine, Terryn, Wim, Callens, Steven, Depypere, Bernard, Van Dorpe, Jo, Poppe, Bruce, Impens, Francis, Mizushima, Noboru, Depienne, Christel, Jéru, Isabelle, Dermaut, Bart

“…Phospholipase A/acyltransferase 3 (PLAAT3) is a phospholipid-modifying enzyme predominantly expressed in neural and white adipose tissue (WAT). It is a…”
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Efficacy and tolerance of corticosteroids and methotrexate in patients with juvenile dermatomyositis: a retrospective cohort study by Dabbak, Imène, Rodero, Mathieu P, Aeschlimann, Florence A, Authier, François-Jérôme, Bodemer, Christine, Quartier, Pierre, Bondet, Vincent, Charuel, Jean-Luc, Duffy, Darragh, Gitiaux, Cyril, Bader-Meunier, Brigitte

“…To assess the efficacy and tolerance of the conventional first-line treatment by methotrexate (MTX) and corticosteroids (CS) in patients with juvenile…”
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The role of aluminum adjuvants in vaccines raises issues that deserve independent, rigorous and honest science by Crépeaux, Guillemette, Authier, François-Jérôme, Exley, Christopher, Luján, Lluís, Gherardi, Romain K.

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Slow CCL2-dependent translocation of biopersistent particles from muscle to brain by Khan, Zakir, Combadière, Christophe, Authier, François-Jérôme, Itier, Valérie, Lux, François, Exley, Christopher, Mahrouf-Yorgov, Meriem, Decrouy, Xavier, Moretto, Philippe, Tillement, Olivier, Gherardi, Romain K, Cadusseau, Josette

“…Long-term biodistribution of nanomaterials used in medicine is largely unknown. This is the case for alum, the most widely used vaccine adjuvant, which is a…”
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Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cells by Cardone, Nastasia, Taglietti, Valentina, Baratto, Serena, Kefi, Kaouthar, Periou, Baptiste, Gitiaux, Ciryl, Barnerias, Christine, Lafuste, Peggy, Pharm, France Leturcq, Pharm, Juliette Nectoux, Panicucci, Chiara, Desguerre, Isabelle, Bruno, Claudio, Authier, François-Jerome, Fiorillo, Chiara, Relaix, Frederic, Malfatti, Edoardo

“…Duchenne muscular dystrophy (DMD) is a devastating X-linked muscular disease, caused by mutations in the DMD gene encoding Dystrophin and affecting 1:5000 boys…”
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An early onset benign myopathy with glycogen storage caused by a de novo 1.4 Mb-deletion of chromosome 14 by Severa, Gianmarco, Pennisi, Alessandra, Barnerias, Christine, Fiorillo, Chiara, Scala, Marcello, Taglietti, Valentina, Cojocaru, Andreea Iuliana, Jouni, Dima, Tosca, Lucie, Tachdjian, Gérard, Desguerre, Isabelle, Authier, François-Jérome, Carlier, Robert-Yves, Metay, Corinne, Verebi, Camille, Malfatti, Edoardo

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