Análisis de las relaciones entre la inteligencia emocional y factores asociados a la calidad de vida

por Ruvalcaba Romero, Norma Alicia, Fernández Berrocal, Pablo, Salazar Estrada, José Guadalupe
Publicado 2014

A Premature Stop Codon in MYO18B is Associated with Severe Nemaline Myopathy with Cardiomyopathy

por Malfatti, Edoardo, Böhm, Johann, Lacène, Emmanuelle, Beuvin, Maud, Guy Brochier, Romero, Norma B., Laporte, Jocelyn
Publicado 2015

Extensive morphological and immunohistochemical characterization in myotubular myopathy

por Shichiji, Minobu, Biancalana, Valérie, Fardeau, Michel, Hogrel, Jean-Yves, Osawa, Makiko, Laporte, Jocelyn, Romero, Norma Beatriz
Publicado 2013

Physiological impact and disease reversion for the severe form of centronuclear myopathy linked to dynamin

por Muñoz, Xènia Massana, Kretz, Christine, Silva-Rojas, Roberto, Ochala, Julien, Menuet, Alexia, Romero, Norma B., Cowling, Belinda S., Laporte, Jocelyn
Publicado 2020

Diagnostic work-up and phenotypic characteristics of a family with variable severity of distal arthrogryposis type 2B (Sheldon-Hall syndrome) and TNNT3 pathogenic variant

por Dabaj, Ivana, Carlier, Robert Y., Dieterich, Klaus, Desguerre, Isabelle, Faure, Julien, Romero, Norma B., Trang, Wenting, Quijano-Roy, Susana, Germain, Dominique P.
Publicado 2023

Some DNM2 mutations cause extremely severe congenital myopathy and phenocopy myotubular myopathy

por Biancalana, Valérie, Romero, Norma B., Thuestad, Inger Johanne, Ignatius, Jaakko, Kataja, Janne, Gardberg, Maria, Héron, Delphine, Malfatti, Edoardo, Oldfors, Anders, Laporte, Jocelyn
Publicado 2018

Benefits of therapy by dynamin-2-mutant-specific silencing are maintained with time in a mouse model of dominant centronuclear myopathy

por Trochet, Delphine, Prudhon, Bernard, Mekzine, Lylia, Lemaitre, Mégane, Beuvin, Maud, Julien, Laura, Benkhelifa-Ziyyat, Sofia, Bui, Mai Thao, Romero, Norma, Bitoun, Marc
Publicado 2022

Comprehensive morphometric assessment of deltoid muscle development in children: A cross-sectional study

por Evangelista, Teresinha, Kandji, Malick, Lacene, Emmanuelle, Chanut, Anaïs, Bui, Mai Thao, Marty, Rudy, Buffat, Laurent, Knoblauch, Kenneth, Rudkin, Brian B., Romero, Norma Beatriz
Publicado 2022

Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth

por Owens, Daniel J., Messéant, Julien, Moog, Sophie, Viggars, Mark, Ferry, Arnaud, Mamchaoui, Kamel, Lacène, Emmanuelle, Roméro, Norma, Brull, Astrid, Bonne, Gisèle, Butler-Browne, Gillian, Coirault, Catherine
Publicado 2020

Knowledge about COVID-19 between Children and Adolescents with and without High Intellectual Abilities

por López-Aymes, Gabriela, Valadez Sierra, María de los Dolores, Borges, África, Ortiz Coronel, Grecia Emilia, Flores-Bravo, Juan Francisco, Rodríguez-Cervantes, Celia Josefina, Ruvalcaba-Romero, Norma A.
Publicado 2023

Expression of myogenic regulatory factors and myo-endothelial remodeling in sporadic inclusion body myositis

por Wanschitz, Julia V., Dubourg, Odile, Lacene, Emmanuelle, Fischer, Michael B., Höftberger, Romana, Budka, Herbert, Romero, Norma B., Eymard, Bruno, Herson, Serge, Butler-Browne, Gillian S., Voit, Thomas, Benveniste, Olivier
Publicado 2013

Autosomal dominant eccentric core disease caused by a heterozygous mutation in the MYH7 gene

por Romero, Norma B, Xie, Ting, Malfatti, Edoardo, Schaeffer, Ursula, Böhm, Johann, Wu, Bin, Xu, Fengping, Boucebci, Samy, Mathis, Stéphane, Neau, Jean-Philippe, Monnier, Nicole, Fardeau, Michel, Laporte, Jocelyn
Publicado 2014

Novel Phenotypes and Cardiac Involvement Associated With DNA2 Genetic Variants

por González-del Angel, Ariadna, Bisciglia, Michela, Vargas-Cañas, Steven, Fernandez-Valverde, Francisca, Kazakova, Ekaterina, Escobar, Rosa Elena, Romero, Norma B., Jardel, Claude, Rucheton, Benoit, Stojkovic, Tanya, Malfatti, Edoardo
Publicado 2019

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

Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscle

por Franck, Agathe, Lainé, Jeanne, Moulay, Gilles, Lemerle, Eline, Trichet, Michaël, Gentil, Christel, Benkhelifa-Ziyyat, Sofia, Lacène, Emmanuelle, Bui, Mai Thao, Brochier, Guy, Guicheney, Pascale, Romero, Norma, Bitoun, Marc, Vassilopoulos, Stéphane
Publicado 2019

Factor structure and internal reliability of an exercise health belief model scale in a Mexican population

por Villar, Oscar Armando Esparza-Del, Montañez-Alvarado, Priscila, Gutiérrez-Vega, Marisela, Carrillo-Saucedo, Irene Concepción, Gurrola-Peña, Gloria Margarita, Ruvalcaba-Romero, Norma Alicia, García-Sánchez, María Dolores, Ochoa-Alcaraz, Sergio Gabriel
Publicado 2017

A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency

por Perrin, Aurélien, Metay, Corinne, Villanova, Marcello, Carlier, Robert‐Yves, Pegoraro, Elena, Juntas Morales, Raul, Stojkovic, Tanya, Richard, Isabelle, Richard, Pascale, Romero, Norma B., Granzier, Henk, Koenig, Michel, Malfatti, Edoardo, Cossée, Mireille
Publicado 2020

rAAV-related therapy fully rescues myonuclear and myofilament function in X-linked myotubular myopathy

por Ross, Jacob A., Tasfaout, Hichem, Levy, Yotam, Morgan, Jennifer, Cowling, Belinda S., Laporte, Jocelyn, Zanoteli, Edmar, Romero, Norma B., Lowe, Dawn A., Jungbluth, Heinz, Lawlor, Michael W., Mack, David L., Ochala, Julien
Publicado 2020

Clinical, histological, and genetic characterization of PYROXD1-related myopathy

por Lornage, Xavière, Schartner, Vanessa, Balbueno, Inès, Biancalana, Valérie, Willis, Tracey, Echaniz-Laguna, Andoni, Scheidecker, Sophie, Quinlivan, Ros, Fardeau, Michel, Malfatti, Edoardo, Lannes, Béatrice, Sewry, Caroline, Romero, Norma B., Laporte, Jocelyn, Böhm, Johann
Publicado 2019

N-WASP is required for Amphiphysin-2/BIN1-dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy

por Falcone, Sestina, Roman, William, Hnia, Karim, Gache, Vincent, Didier, Nathalie, Lainé, Jeanne, Auradé, Frederic, Marty, Isabelle, Nishino, Ichizo, Charlet-Berguerand, Nicolas, Romero, Norma Beatriz, Marazzi, Giovanna, Sassoon, David, Laporte, Jocelyn, Gomes, Edgar R
Publicado 2014