Congenital oro-motor disorders von Roig Quilis, Manuel

Volltext

Muscle genome-wide expression profiling during disease evolution in mdx mice von Marotta, Mario, Ruiz-Roig, Claudia, Sarria, Yaris, Peiro, Jose Luis, Nunez, Fatima, Ceron, Julian, Munell, Francina, Roig-Quilis, Manuel

Volltext

Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy von Juan-Mateu, Jonàs, Rodríguez, Maria José, Nascimento, Andrés, Jiménez-Mallebrera, Cecilia, González-Quereda, Lidia, Rivas, Eloy, Paradas, Carmen, Madruga, Marcos, Sánchez-Ayaso, Pedro, Jou, Cristina, González-Mera, Laura, Munell, Francina, Roig-Quilis, Manuel, Rabasa, Maria, Hernández-Lain, Aurelio, Díaz-Manera, Jorge, Gallardo, Eduard, Pascual, Jordi, Verdura, Edgard, Colomer, Jaume, Baiget, Montserrat, Olivé, Montse, Gallano, Pia

Volltext

Central Hypoventilation and Brainstem Dysgenesis von Armangue, Thais, MD, Macaya, Alfons, MD, PhD, Vazquez, Elida, MD, Jurado, Maria José, MD, Roig-Quilis, Manuel, MD, PhD

Volltext

Brainstem Dysgenesis in an Infant Prenatally Exposed to Cocaine von Boix, Hector, MD, Ortega-Aznar, Arantxa, MD, Vazquez, Elida, MD, Salcedo, Salvador, MD, Roig-Quilis, Manuel, MD, PhD

Volltext

Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential no... von Kalko, Susana Graciela, Paco, Sonia, Jou, Cristina, Rodríguez, Maria Angels, Meznaric, Marija, Rogac, Mihael, Jekovec-Vrhovsek, Maja, Sciacco, Monica, Moggio, Maurizio, Fagiolari, Gigliola, De Paepe, Boel, De Meirleir, Linda, Ferrer, Isidre, Roig-Quilis, Manel, Munell, Francina, Montoya, Julio, López-Gallardo, Ester, Ruiz-Pesini, Eduardo, Artuch, Rafael, Montero, Raquel, Torner, Ferran, Nascimento, Andres, Ortez, Carlos, Colomer, Jaume, Jimenez-Mallebrera, Cecilia

Volltext

Etanercept-Induced Myelopathy in a Pediatric Case of Blau Syndrome von Caracseghi, Fabiola, Roig-Quilis, Manuel, Sanchez-Montanez, Angel, Melendo-Perez, Susana, Modesto, Consuelo, Izquierdo-Blasco, Jaume

Volltext

Leigh Syndrome and the Mitochondrial m.13513G>A Mutation: Expanding the Clinical Spectrum von Monlleo-Neila, Laura, Toro, Mireia del, Bornstein, Belen, Garcia-Arumi, Elena, Sarrias, Axel, Roig-Quilis, Manuel, Munell, Francina

Volltext

Brainstem dysgenesis: beyond Moebius syndrome von Munell, F, Tormos, M A, Roig-Quilis, M

Volltext

Paroxysmal exercise-induced dyskinesia, writer's cramp, migraine with aura and absence epilepsy in twin brothers with a novel SLC2A1 missense mutation von Urbizu, Aintzane, Cuenca-León, Ester, Raspall-Chaure, Miquel, Gratacòs, Margarida, Conill, Joan, Redecillas, Susana, Roig-Quilis, Manuel, Macaya, Alfons

Volltext

Congenital oro‐motor disorders von Quilis, Manuel Roig

Volltext

Laser microdissection-based expression analysis of key genes involved in muscle regeneration in mdx mice von Marotta, Mario, Sarria, Yaris, Ruiz-Roig, Claudia, Munell, Francina, Roig-Quilis, Manuel

Volltext

Brainstem dysgenesis during the neonatal period: diagnosis and management von Castilla-Fernández, Yolanda, Boix, Héctor, Macaya, Alfons, Vázquez, Elida, Gratacòs, Margarida, Roig-Quilis, Manuel

Volltext

Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential no... von Kalko, Susana, Paco Mercader, Sonia, Jou, Cristina, Rodríguez, María Angeles, Meznaric, Marija, Rogac, Mihael, Jekovec-Vrhovsek, Maja, Sciacco, Monica, Moggio, Maurizio, Fagiolari, Gigliola, De Paepe, Boel, De Meirleir, Linda, Ferrer, Isidro (Ferrer Abizanda), Roig Quilis, Manuel, Munell Casadesús, Francina, Montoya, Julio, López Gallardo, Ester, Ruiz Pesini, Eduardo, Artuch Iriberri, Rafael, Montero Sánchez, Raquel, Torner Rubies, Ferran, Nascimento, Andrés, Ortez, Carlos Ignacio, Colomer Oferil, Jaume, Jiménez Mallebrera, Cecilia

Volltext

Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential no... von Kalko, Susana, Paco Mercader, Sonia, Jou, Cristina, Rodríguez, Maria Angels, Meznaric, Marija, Rogac, Mihael, Jekovec-Vrhovsek, Maja, Sciacco, Monica, Moggio, Maurizio, Fagiolari, Gigliola, De Paepe, Boel, De Meirleir, Linda, Ferrer, Isidro (Ferrer Abizanda), Roig Quilis, Manuel, Munell Casadesús, Francina, Montoya, Julio, López-Gallardo, Ester, Ruiz-Pesini, Eduardo, Artuch Iriberri, Rafael, Montero Sánchez, Raquel, Torner Rubies, Ferran, Nascimento, Andrés, Ortez, Carlos Ignacio, Colomer, Jaume, Jiménez Mallebrera, Cecilia

Volltext

Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential no... von Kalko, Susana, Paco Mercader, Sonia, Jou, Cristina, Rodríguez, Maria Angels, Meznaric, Marija, Rogac, Mihael, Jekovec-Vrhovsek, Maja, Sciacco, Monica, Moggio, Maurizio, Fagiolari, Gigliola, De Paepe, Boel, De Meirleir, Linda, Ferrer, Isidro (Ferrer Abizanda), Roig Quilis, Manuel, Munell Casadesús, Francina, Montoya, Julio, López-Gallardo, Ester, Ruiz-Pesini, Eduardo, Artuch Iriberri, Rafael, Montero Sánchez, Raquel, Torner Rubies, Ferran, Nascimento, Andrés, Ortez, Carlos Ignacio, Colomer, Jaume, Jiménez Mallebrera, Cecilia

Volltext

Reversible encephalopathy caused by valproic acid in an adolescent with idiopathic generalised epilepsy von Raspall-Chaure, Miquel, Lainez, Elena, Toledo, Manuel, Salas-Puig, Javier, Macaya-Ruiz, Alfons, Roig-Quilis, Manuel

Volltext

Clinical variability of polymicrogiria: report of 35 new cases and review of the literature von Flotats-Bastardas, Marina, Sánchez-Montañez, Ángel, Vázquez-Méndez, Elida, Ortega-Aznar, Arantxa, Boronat-Guerrero, Susanna, Raspall-Chaure, Miquel, del Toro-Riera, Mireia, Munell, Francina, Macaya-Ruiz, Alfons, Roig-Quilis, Manuel

Volltext

Trastornos oromotores en una unidad de neurología pediátrica. Clasificación y evolución clínica von Roig Quilis, Manel, Rodríguez Palmero, Agustí

Volltext

Microcefàlia en la infància: estudi evolutiu i pronòstic von Coronado Contreras, Ricard, Universitat Autònoma de Barcelona. Departament de Pediatria, d'Obstetrícia i Ginecologia i de Medicina Preventiva

Volltext bestellen