Vertebroepidural metastasis of an ethmoid adenocarcinoma: A case report

por MBAYE, MAGUETTE, POPA, CLAUDIU, SIGNORELLI, FRANCESCO, STREICHENBERGER, NATHALIE, COSMIDIS, ALAIN, POZZI, FABIO, GUYOTAT, JACQUES
Publicado 2013

Phosphorylation of NBR1 by GSK3 modulates protein aggregation

por Nicot, Anne-Sophie, Lo Verso, Francesca, Ratti, Francesca, Pilot-Storck, Fanny, Streichenberger, Nathalie, Sandri, Marco, Schaeffer, Laurent, Goillot, Evelyne
Publicado 2014

SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells

por Janin, Alexandre, Bauer, Delphine, Ratti, Francesca, Valla, Camille, Bertrand, Anne, Christin, Emilie, Chopin, Emilie, Streichenberger, Nathalie, Bonne, Gisèle, Gache, Vincent, Cohen, Tatiana, Méjat, Alexandre
Publicado 2018

Revisiting idiopathic eosinophilic myositis: towards a clinical-pathological continuum from the muscle to the fascia and skin

por Fermon, Cécile, Lessard, Lola E R, Fenouil, Tanguy, Meyer, Alain, Faruch-Bilfeld, Marie, Robert, Marie, Landel, Verena, Hot, Arnaud, Authier, François-Jérôme, Streichenberger, Nathalie, Gallay, Laure
Publicado 2022

Tau pathology in Creutzfeldt‐Jakob disease revisited

por Kovacs, Gabor G., Rahimi, Jasmin, Ströbel, Thomas, Lutz, Mirjam I., Regelsberger, Günther, Streichenberger, Nathalie, Perret‐Liaudet, Armand, Höftberger, Romana, Liberski, Pawel P., Budka, Herbert, Sikorska, Beata
Publicado 2016

BrainNet Europe’s Code of Conduct for brain banking

por Klioueva, Natasja M., Rademaker, Marleen C., Dexter, David T., Al-Sarraj, Safa, Seilhean, Danielle, Streichenberger, Nathalie, Schmitz, Peer, Bell, Jeanne E., Ironside, James W., Arzberger, Thomas, Huitinga, Inge
Publicado 2015

Latency Entry of Herpes Simplex Virus 1 Is Determined by the Interaction of Its Genome with the Nuclear Environment

por Maroui, Mohamed Ali, Callé, Aleth, Cohen, Camille, Streichenberger, Nathalie, Texier, Pascale, Takissian, Julie, Rousseau, Antoine, Poccardi, Nolwenn, Welsch, Jérémy, Corpet, Armelle, Schaeffer, Laurent, Labetoulle, Marc, Lomonte, Patrick
Publicado 2016

Lack of muscle mTOR kinase activity causes early onset myopathy and compromises whole‐body homeostasis

por Zhang, Qing, Duplany, Agnès, Moncollin, Vincent, Mouradian, Sandrine, Goillot, Evelyne, Mazelin, Laetitia, Gauthier, Karine, Streichenberger, Nathalie, Angleraux, Céline, Chen, Jie, Ding, Shuzhe, Schaeffer, Laurent, Gangloff, Yann‐Gaël
Publicado 2018

Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy—Case Report

por Pegat, Antoine, Streichenberger, Nathalie, Lacoste, Nicolas, Hermier, Marc, Menassa, Rita, Coudert, Laurent, Theuriet, Julian, Froissart, Roseline, Terrone, Sophie, Bouhour, Francoise, Michel-Calemard, Laurence, Schaeffer, Laurent, Jacquier, Arnaud
Publicado 2022

Experimental transfusion of variant CJD-infected blood reveals previously uncharacterised prion disorder in mice and macaque

por Comoy, Emmanuel E., Mikol, Jacqueline, Jaffré, Nina, Lebon, Vincent, Levavasseur, Etienne, Streichenberger, Nathalie, Sumian, Chryslain, Perret-Liaudet, Armand, Eloit, Marc, Andreoletti, Olivier, Haïk, Stéphane, Hantraye, Philippe, Deslys, Jean-Philippe
Publicado 2017

Facioscapulohumeral dystrophy weakened sarcomeric contractility is mimicked in induced pluripotent stem cells‐derived innervated muscle fibres

por Laberthonnière, Camille, Novoa‐del‐Toro, Elva‐Maria, Delourme, Mégane, Chevalier, Raphaël, Broucqsault, Natacha, Mazaleyrat, Kilian, Streichenberger, Nathalie, Manel, Véronique, Bernard, Rafaëlle, Salort Campana, Emmanuelle, Attarian, Shahram, Nguyen, Karine, Robin, Jérôme D., Baudot, Anais, Magdinier, Frédérique
Publicado 2021

Preclinical Detection of Variant CJD and BSE Prions in Blood

por Lacroux, Caroline, Comoy, Emmanuel, Moudjou, Mohammed, Perret-Liaudet, Armand, Lugan, Séverine, Litaise, Claire, Simmons, Hugh, Jas-Duval, Christelle, Lantier, Isabelle, Béringue, Vincent, Groschup, Martin, Fichet, Guillaume, Costes, Pierrette, Streichenberger, Nathalie, Lantier, Frederic, Deslys, Jean Philippe, Vilette, Didier, Andréoletti, Olivier
Publicado 2014

Beyond PrP(res) Type 1/Type 2 Dichotomy in Creutzfeldt-Jakob Disease

por Uro-Coste, Emmanuelle, Cassard, Hervé, Simon, Stéphanie, Lugan, Séverine, Bilheude, Jean-Marc, Perret-Liaudet, Armand, Ironside, James W., Haik, Stéphane, Basset-Leobon, Christelle, Lacroux, Caroline, Peoch', Katell, Streichenberger, Nathalie, Langeveld, Jan, Head, Mark W., Grassi, Jacques, Hauw, Jean-Jacques, Schelcher, Francois, Delisle, Marie Bernadette, Andréoletti, Olivier
Publicado 2008

Altered Ca(2+) homeostasis induces Calpain-Cathepsin axis activation in sporadic Creutzfeldt-Jakob disease

por Llorens, Franc, Thüne, Katrin, Sikorska, Beata, Schmitz, Matthias, Tahir, Waqas, Fernández-Borges, Natalia, Cramm, Maria, Gotzmann, Nadine, Carmona, Margarita, Streichenberger, Nathalie, Michel, Uwe, Zafar, Saima, Schuetz, Anna-Lena, Rajput, Ashish, Andréoletti, Olivier, Bonn, Stefan, Fischer, Andre, Liberski, Pawel P., Torres, Juan Maria, Ferrer, Isidre, Zerr, Inga
Publicado 2017

Immune-Mediated Rippling Muscle Disease Associated With Thymoma and Anti-MURC/Cavin-4 Autoantibodies

por Svahn, Juliette, Coudert, Laurent, Streichenberger, Nathalie, Kraut, Alexandra, Gravier-Dumonceau-Mazelier, Alice, Rotard, Ludivine, Calemard-Michel, Laurence, Menassa, Rita, Errazuriz-Cerda, Elisabeth, Chalabreysse, Lara, Osseni, Alexis, Vial, Christophe, Jomir, Laurentiu, Tronc, François, Le Duy, Do, Bernard, Emilien, Gache, Vincent, Couté, Yohann, Jacquemond, Vincent, Schaeffer, Laurent, Leblanc, Pascal
Publicado 2022

Prion strains associated with iatrogenic CJD in French and UK human growth hormone recipients

por Douet, Jean-Yves, Huor, Alvina, Cassard, Hervé, Lugan, Séverine, Aron, Naïma, Mesic, Chloé, Vilette, Didier, Barrio, Tomás, Streichenberger, Nathalie, Perret-Liaudet, Armand, Delisle, Marie-Bernadette, Péran, Patrice, Deslys, Jean-Philippe, Comoy, Emmanuel, Vilotte, Jean-Luc, Goudarzi, Katayoun, Béringue, Vincent, Barria, Marcelo A., Ritchie, Diane L., Ironside, James W., Andréoletti, Olivier
Publicado 2021

Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency

por Ben Yaou, Rabah, Hubert, Aurélie, Nelson, Isabelle, Dahlqvist, Julia R., Gaist, David, Streichenberger, Nathalie, Beuvin, Maud, Krahn, Martin, Petiot, Philippe, Parisot, Frédéric, Michel, Fabrice, Malfatti, Edoardo, Romero, Norma, Carlier, Robert Yves, Eymard, Bruno, Labrune, Philippe, Duno, Morten, Krag, Thomas, Cerino, Mathieu, Bartoli, Marc, Bonne, Gisèle, Vissing, John, Laforet, Pascal, Petit, François M.
Publicado 2017

Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairment

por Laforêt, Pascal, Inoue, Michio, Goillot, Evelyne, Lefeuvre, Claire, Cagin, Umut, Streichenberger, Nathalie, Leonard-Louis, Sarah, Brochier, Guy, Madelaine, Angeline, Labasse, Clemence, Hedberg-Oldfors, Carola, Krag, Thomas, Jauze, Louisa, Fabregue, Julien, Labrune, Philippe, Milisenda, Jose, Nadaj-Pakleza, Aleksandra, Sacconi, Sabrina, Mingozzi, Federico, Ronzitti, Giuseppe, Petit, François, Schoser, Benedikt, Oldfors, Anders, Vissing, John, Romero, Norma B., Nishino, Ichizo, Malfatti, Edoardo
Publicado 2019

Staging of Neurofibrillary Pathology in Alzheimer's Disease: A Study of the BrainNet Europe Consortium

por Alafuzoff, Irina, Arzberger, Thomas, Al‐Sarraj, Safa, Bodi, Istvan, Bogdanovic, Nenad, Braak, Heiko, Bugiani, Orso, Del‐Tredici, Kelly, Ferrer, Isidro, Gelpi, Ellen, Giaccone, Giorgio, Graeber, Manuel B., Ince, Paul, Kamphorst, Wouter, King, Andrew, Korkolopoulou, Penelope, Kovács, Gábor G., Larionov, Sergey, Meyronet, David, Monoranu, Camelia, Parchi, Piero, Patsouris, Efstratios, Roggendorf, Wolfgang, Seilhean, Danielle, Tagliavini, Fabrizio, Stadelmann, Christine, Streichenberger, Nathalie, Thal, Dietmar R., Wharton, Stephen B, Kretzschmar, Hans
Publicado 2008

Skeletal muscle provides the immunological micro-milieu for specific plasma cells in anti-synthetase syndrome-associated myositis

por Preuße, Corinna, Paesler, Barbara, Nelke, Christopher, Cengiz, Derya, Müntefering, Thomas, Roos, Andreas, Amelin, Damien, Allenbach, Yves, Uruha, Akinori, Dittmayer, Carsten, Hentschel, Andreas, Pawlitzki, Marc, Hoffmann, Sarah, Timm, Sara, Louis, Sarah Leonard, Dengler, Nora F., Wiendl, Heinz, Lünemann, Jan D., Sickmann, Albert, Hervier, Baptiste, Meuth, Sven G., Schneider, Udo, Schänzer, Anne, Krause, Sabine, Tomaras, Stylianos, Feist, Eugen, Hasseli, Rebecca, Goebel, Hans-Hilmar, Gallay, Laure, Streichenberger, Nathalie, Benveniste, Olivier, Stenzel, Werner, Ruck, Tobias
Publicado 2022