Vessel-associated stem cells from skeletal muscle: From biology to future uses in cell therapy

por Sancricca, Cristina, Mirabella, Massimiliano, Gliubizzi, Carla, Broccolini, Aldobrando, Gidaro, Teresa, Morosetti, Roberta
Publicado em 2010

Relationship between markers of disease activity and progression in skeletal muscle of GNE myopathy patients using quantitative nuclear magnetic resonance imaging and (31)P nuclear...

por Reyngoudt, Harmen, Marty, Benjamin, Caldas de Almeida Araújo, Ericky, Baudin, Pierre-Yves, Le Louër, Julien, Boisserie, Jean-Marc, Béhin, Anthony, Servais, Laurent, Gidaro, Teresa, Carlier, Pierre G.
Publicado no Quant Imaging Med Surg (2020)

MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle

por Morosetti, Roberta, Mirabella, Massimiliano, Gliubizzi, Carla, Broccolini, Aldobrando, De Angelis, Luciana, Tagliafico, Enrico, Sampaolesi, Maurilio, Gidaro, Teresa, Papacci, Manuela, Roncaglia, Enrica, Rutella, Sergio, Ferrari, Stefano, Tonali, Pietro Attilio, Ricci, Enzo, Cossu, Giulio
Publicado em 2006

PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy –Consequences in Clinical Diagnosis and Genetic Counselling

por Richard, Pascale, Trollet, Capucine, Gidaro, Teresa, Demay, Laurence, Brochier, Guy, Malfatti, Edoardo, Tom, Fernando MS, Fardeau, Michel, Lafor, Pascal, Romero, Norma, Martin-N, Marie-Laure, Sol, Guilhem, Ferrer-Monasterio, Xavier, Saint-Guily, Jean Lacau, Eymard, Bruno
Publicado no J Neuromuscul Dis (2015)

Longitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy

por Hogrel, Jean-Yves, Wary, Claire, Moraux, Amélie, Azzabou, Noura, Decostre, Valérie, Ollivier, Gwenn, Canal, Aurélie, Lilien, Charlotte, Ledoux, Isabelle, Annoussamy, Mélanie, Reguiba, Nacera, Gidaro, Teresa, Le Moing, Anne Gaelle, Cardas, Ruxandra, Voit, Thomas, Carlier, Pierre G., Servais, Laurent
Publicado no Neurology (2016)

Rimeporide as a first- in-class NHE-1 inhibitor: Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy

por Previtali, Stefano C., Gidaro, Teresa, Díaz-Manera, Jordi, Zambon, Alberto, Carnesecchi, Stephanie, Roux-Lombard, Pascale, Spitali, Pietro, Signorelli, Mirko, Szigyarto, Cristina Al-Khalili, Johansson, Camilla, Gray, Julian, Labolle, Delphine, Porte Thomé, Florence, Pitchforth, Jacqueline, Domingos, Joana, Muntoni, Francesco
Publicado no Pharmacol Res (2020)

Mitochondrial Dysfunction Reveals the Role of mRNA Poly(A) Tail Regulation in Oculopharyngeal Muscular Dystrophy Pathogenesis

por Chartier, Aymeric, Klein, Pierre, Pierson, Stéphanie, Barbezier, Nicolas, Gidaro, Teresa, Casas, François, Carberry, Steven, Dowling, Paul, Maynadier, Laurie, Bellec, Maëlle, Oloko, Martine, Jardel, Claude, Moritz, Bodo, Dickson, George, Mouly, Vincent, Ohlendieck, Kay, Butler-Browne, Gillian, Trollet, Capucine, Simonelig, Martine
Publicado no PLoS Genet (2015)

Nuclear poly(A)-binding protein aggregates misplace a pre-mRNA outside of SC35 speckle causing its abnormal splicing

por Klein, Pierre, Oloko, Martine, Roth, Fanny, Montel, Valérie, Malerba, Alberto, Jarmin, Susan, Gidaro, Teresa, Popplewell, Linda, Perie, Sophie, Lacau St Guily, Jean, de la Grange, Pierre, Antoniou, Michael N., Dickson, George, Butler-Browne, Gillian, Bastide, Bruno, Mouly, Vincent, Trollet, Capucine
Publicado no Nucleic Acids Res (2016)

Non-Ambulant Duchenne Patients Theoretically Treatable by Exon 53 Skipping have Severe Phenotype

por Servais, Laurent, Montus, Marie, Guiner, Caroline Le, Ben Yaou, Rabah, Annoussamy, Mélanie, Moraux, Amélie, Hogrel, Jean-Yves, Seferian, Andreea M., Zehrouni, Karima, Le Moing, Anne-Gaëlle, Gidaro, Teresa, Vanhulle, Catherine, Laugel, Vincent, Butoianu, Nina, Cuisset, Jean-Marie, Sabouraud, Pascal, Cances, Claude, Klein, Andrea, Leturcq, France, Moullier, Philippe, Voit, Thomas
Publicado no J Neuromuscul Dis (2015)

Natural history of Type 2 and 3 spinal muscular atrophy: 2‐year NatHis‐SMA study

por Annoussamy, Mélanie, Seferian, Andreea M., Daron, Aurore, Péréon, Yann, Cances, Claude, Vuillerot, Carole, De Waele, Liesbeth, Laugel, Vincent, Schara, Ulrike, Gidaro, Teresa, Lilien, Charlotte, Hogrel, Jean‐Yves, Carlier, Pierre, Fournier, Emmanuel, Lowes, Linda, Gorni, Ksenija, Ly‐Le Moal, Myriam, Hellbach, Nicole, Seabrook, Timothy, Czech, Christian, Hermosilla, Ricardo, Servais, Laurent
Publicado no Ann Clin Transl Neurol (2020)

Upper Limb Evaluation and One-Year Follow Up of Non-Ambulant Patients with Spinal Muscular Atrophy: An Observational Multicenter Trial

por Seferian, Andreea Mihaela, Moraux, Amélie, Canal, Aurélie, Decostre, Valérie, Diebate, Oumar, Le Moing, Anne Gaëlle, Gidaro, Teresa, Deconinck, Nicolas, Van Parys, Frauke, Vereecke, Wendy, Wittevrongel, Sylvia, Annoussamy, Mélanie, Mayer, Michèle, Maincent, Kim, Cuisset, Jean-Marie, Tiffreau, Vincent, Denis, Severine, Jousten, Virginie, Quijano-Roy, Susana, Voit, Thomas, Hogrel, Jean-Yves, Servais, Laurent
Publicado no PLoS One (2015)

Prospective and longitudinal natural history study of patients with Type 2 and 3 spinal muscular atrophy: Baseline data NatHis-SMA study

por Chabanon, Aurélie, Seferian, Andreea Mihaela, Daron, Aurore, Péréon, Yann, Cances, Claude, Vuillerot, Carole, De Waele, Liesbeth, Cuisset, Jean-Marie, Laugel, Vincent, Schara, Ulrike, Gidaro, Teresa, Gilabert, Stéphanie, Hogrel, Jean-Yves, Baudin, Pierre-Yves, Carlier, Pierre, Fournier, Emmanuel, Lowes, Linda Pax, Hellbach, Nicole, Seabrook, Timothy, Toledano, Elie, Annoussamy, Mélanie, Servais, Laurent
Publicado no PLoS One (2018)

X-linked myotubular myopathy: A prospective international natural history study

por Annoussamy, Mélanie, Lilien, Charlotte, Gidaro, Teresa, Gargaun, Elena, Chê, Virginie, Schara, Ulrike, Gangfuß, Andrea, D'Amico, Adele, Dowling, James J., Darras, Basil T., Daron, Aurore, Hernandez, Arturo, de Lattre, Capucine, Arnal, Jean-Michel, Mayer, Michèle, Cuisset, Jean-Marie, Vuillerot, Carole, Fontaine, Stéphanie, Bellance, Rémi, Biancalana, Valérie, Buj-Bello, Ana, Hogrel, Jean-Yves, Landy, Hal, Servais, Laurent
Publicado no Neurology (2019)

ASC1 is a cell cycle regulator associated with severe and mild forms of myopathy

por Villar-Quiles, Rocío N, Catervi, Fabio, Cabet, Eva, Juntas-Morales, Raul, Genetti, Casie A., Gidaro, Teresa, Koparir, Asuman, Yüksel, Adnan, Coppens, Sandra, Deconinck, Nicolas, Pierce-Hoffman, Emma, Lornage, Xavière, Durigneux, Julien, Laporte, Jocelyn, Rendu, John, Romero, Norma B., Beggs, Alan H., Servais, Laurent, Cossée, Mireille, Olivé, Montse, Böhm, Johann, Duband-Goulet, Isabelle, Ferreiro, Ana
Publicado no Ann Neurol (2019)

Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial

por Seferian, Andreea Mihaela, Moraux, Amélie, Annoussamy, Mélanie, Canal, Aurélie, Decostre, Valérie, Diebate, Oumar, Le Moing, Anne-Gaëlle, Gidaro, Teresa, Deconinck, Nicolas, Van Parys, Frauke, Vereecke, Wendy, Wittevrongel, Sylvia, Mayer, Michèle, Maincent, Kim, Desguerre, Isabelle, Thémar-Noël, Christine, Cuisset, Jean-Marie, Tiffreau, Vincent, Denis, Severine, Jousten, Virginie, Quijano-Roy, Susana, Voit, Thomas, Hogrel, Jean-Yves, Servais, Laurent
Publicado no PLoS One (2015)