Editorial: Extracellular matrix in homeostasis and cancer

por Carlos, Ana Rita, Allamand, Valérie
Publicado 2022

ColVI myopathies: where do we stand, where do we go?

por Allamand, Valérie, Briñas, Laura, Richard, Pascale, Stojkovic, Tanya, Quijano-Roy, Susana, Bonne, Gisèle
Publicado 2011

Antioxidants Reduce Muscular Dystrophy in the dy(2J)/dy(2J) Mouse Model of Laminin α2 Chain-Deficient Muscular Dystrophy

por Harandi, Vahid M., Moreira Soares Oliveira, Bernardo, Allamand, Valérie, Friberg, Ariana, Fontes-Oliveira, Cibely C., Durbeej, Madeleine
Publicado 2020

Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursors

por Castets, Perrine, Maugenre, Svetlana, Gartioux, Corine, Rederstorff, Mathieu, Krol, Alain, Lescure, Alain, Tajbakhsh, Shahragim, Allamand, Valérie, Guicheney, Pascale
Publicado 2009

Ullrich Congenital Muscular Dystrophy (UCMD): Clinical and Genetic Correlations

por BOZORGMEHR, Bita, KARIMINEJAD, Ariana, NAFISSI, Shahriar, JEBELLI, Bita, ANDONI, Urtizberea, GARTIOUx, Corine, LEDEUIL, Celine, ALLAMAND, Valérie, RICHARD, Pascale, KARIMINEJAD, Mohammad-Hassan
Publicado 2013

A novel COL1A1 variant in a family with clinical features of hypermobile Ehlers‐Danlos syndrome that proved to be a COL1‐related overlap disorder

por Foy, Malika, De Mazancourt, Philippe, Métay, Corinne, Carlier, Robert, Allamand, Valérie, Gartioux, Corine, Gillas, Fabrice, Miri, Nawel, Jobic, Valérie, Mekki, Ahmed, Richard, Pascale, Michot, Caroline, Benistan, Karelle
Publicado 2021

Increased Muscle Stress-Sensitivity Induced by Selenoprotein N Inactivation in Mouse: A Mammalian Model for SEPN1-Related Myopathy

por Rederstorff, Mathieu, Castets, Perrine, Arbogast, Sandrine, Lainé, Jeanne, Vassilopoulos, Stéphane, Beuvin, Maud, Dubourg, Odile, Vignaud, Alban, Ferry, Arnaud, Krol, Alain, Allamand, Valérie, Guicheney, Pascale, Ferreiro, Ana, Lescure, Alain
Publicado 2011

Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related Diseases

por Nelson, Isabelle, Stojkovic, Tanya, Allamand, Valérie, Leturcq, France, Bécane, Henri-Marc, Babuty, Dominique, Toutain, Annick, Béroud, Christophe, Richard, Pascale, Romero, Norma B., Eymard, Bruno, Ben Yaou, Rabah, Bonne, Gisèle
Publicado 2015

Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy

por Rau, Frédérique, Lainé, Jeanne, Ramanoudjame, Laetitita, Ferry, Arnaud, Arandel, Ludovic, Delalande, Olivier, Jollet, Arnaud, Dingli, Florent, Lee, Kuang-Yung, Peccate, Cécile, Lorain, Stéphanie, Kabashi, Edor, Athanasopoulos, Takis, Koo, Taeyoung, Loew, Damarys, Swanson, Maurice S., Le Rumeur, Elisabeth, Dickson, George, Allamand, Valérie, Marie, Joëlle, Furling, Denis
Publicado 2015

Intrafamilial Phenotypic Variability of Collagen VI-Related Myopathy Due to a New Mutation in the COL6A1 Gene

por Bardakov, Sergey N., Deev, Roman V., Magomedova, Raisat M., Umakhanova, Zoya R., Allamand, Valérie, Gartioux, Corine, Zulfugarov, Kamil Z., Akhmedova, Patimat G., Tsargush, Vadim A., Titova, Angelina A., Mavlikeev, Mikhail O., Zorin, Vadim L., Chernets, Ekaterina N., Dalgatov, Gimat D., Konovalov, Fedor A., Isaev, Artur A.
Publicado 2021