Coenzyme Q₁₀ Treatment Monitoring in Different Human Biological Samples by Abraham J. Paredes-Fuentes, Raquel Montero, Anna Codina, Cristina Jou, Guerau Fernández, Joan Maynou, Carlos Santos-Ocaña, Joan Riera, Plácido Navas, Franchek Drobnic, Rafael Artuch

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Transcriptome Analysis of Ullrich Congenital Muscular Dystrophy Fibroblasts Reveals a Disease Extracellular Matrix Signature and Key Molecular Regulators. by Sonia Paco, Teresa Casserras, Maria Angels Rodríguez, Cristina Jou, Montserrat Puigdelloses, Carlos I Ortez, Jordi Diaz-Manera, Eduardo Gallardo, Jaume Colomer, Andrés Nascimento, Susana G Kalko, Cecilia Jimenez-Mallebrera

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Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants by Daniel Natera‐de Benito, Jonathan Olival, Carla Garcia‐Cabau, Cristina Jou, Mònica Roldan, Anna Codina, Jessica Expósito‐Escudero, Cristina Batlle, Laura Carrera‐García, Carlos Ortez, Xavier Salvatella, Francesc Palau, Andrés Nascimento, Janet Hoenicka

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Desensitizing the autonomic nervous system to mitigate anti-GD2 monoclonal antibody side effects by Jaume Mora, Alejandra Climent, Mònica Roldán, Marta Cecilia Flores, Amalia Varo, Sara Perez-Jaume, Cristina Jou, Mónica S. Celma, Juan José Lazaro, Irene Cheung, Alicia Castañeda, Maite Gorostegui, Eva Rodriguez, Saray Chamorro, Juan Pablo Muñoz, Nai-Kong Cheung

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Sphingolipid desaturase DEGS1 is essential for mitochondria-associated membrane integrity by Laura Planas-Serra, Nathalie Launay, Leire Goicoechea, Bénédicte Heron, Cristina Jou, Natalia Juliá-Palacios, Montserrat Ruiz, Stéphane Fourcade, Carlos Casasnovas, Carolina De La Torre, Antoinette Gelot, Maria Marsal, Pablo Loza-Alvarez, Àngels García-Cazorla, Ali Fatemi, Isidre Ferrer, Manel Portero-Otin, Estela Area-Gómez, Aurora Pujol

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Decoding the transcriptome of Duchenne muscular dystrophy to the single nuclei level reveals clinical-genetic correlations by Xavier Suárez-Calvet, Esther Fernández-Simón, Daniel Natera, Cristina Jou, Patricia Pinol-Jurado, Elisa Villalobos, Carlos Ortez, Alexandra Monceau, Marianela Schiava, Anna Codina, José Verdu-Díaz, James Clark, Zoe Laidler, Priyanka Mehra, Rasya Gokul-Nath, Jorge Alonso-Perez, Chiara Marini-Bettolo, Giorgio Tasca, Volker Straub, Michela Guglieri, Andrés Nascimento, Jordi Diaz-Manera

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OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect by Kyle Thompson, Nicole Mai, Monika Oláhová, Filippo Scialó, Luke E Formosa, David A Stroud, Madeleine Garrett, Nichola Z Lax, Fiona M Robertson, Cristina Jou, Andres Nascimento, Carlos Ortez, Cecilia Jimenez‐Mallebrera, Steven A Hardy, Langping He, Garry K Brown, Paula Marttinen, Robert McFarland, Alberto Sanz, Brendan J Battersby, Penelope E Bonnen, Michael T Ryan, Zofia MA Chrzanowska‐Lightowlers, Robert N Lightowlers, Robert W Taylor

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Low transmission of SARS-CoV-2 derived from children in family clusters: An observational study of family households in the Barcelona Metropolitan Area, Spain. by Maria Mele-Casas, Cristian Launes, Mariona F de Sevilla, Maria Hernandez-Garcia, Gemma Pons-Tomas, Quique Bassat, Victoria Fumado, Claudia Fortuny, Aleix Garcia-Miquel, Elisenda Bonet-Carne, Clara Prats, Sara Ajanovic, Marta Cubells, Joana Claverol, Daniel Penela-Sanchez, Cristina Jou, Sara Arias, Nuria Balanza, Barbara Baro, Pere Millat-Martinez, Sergio Alonso, Enric Alvarez-Lacalle, Marti Catala, Daniel Cuadras, Carmen Muñoz-Almagro, Eduard Gratacos, Iolanda Jordan, Juan Jose Garcia-Garcia

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