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

od Sancricca, Cristina, Mirabella, Massimiliano, Gliubizzi, Carla, Broccolini, Aldobrando, Gidaro, Teresa, Morosetti, Roberta
Izdano 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...

od 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.
Izdano u Quant Imaging Med Surg (2020)

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

od 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
Izdano 2006

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

od 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
Izdano u J Neuromuscul Dis (2015)

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

od 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
Izdano u Neurology (2016)

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

od 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
Izdano u Pharmacol Res (2020)

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

od 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
Izdano u PLoS Genet (2015)

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

od 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
Izdano u Nucleic Acids Res (2016)

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

od 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
Izdano u J Neuromuscul Dis (2015)

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

od 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
Izdano u 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

od 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
Izdano u PLoS One (2015)

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

od 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
Izdano u PLoS One (2018)

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

od 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
Izdano u Neurology (2019)

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

od 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
Izdano u 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

od 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
Izdano u PLoS One (2015)