Kết quả tìm kiếm - Daniel Natera‐de Benito
- Đang hiển thị 1 - 6 kết quả của 6
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1
Validation of motor and functional scales for the evaluation of adult patients with 5q spinal muscular atrophy Bằng Juan F. Vázquez‐Costa, Mònica Povedano, Andrés E. Nascimiento‐Osorio, Antonio Moreno Escribano, S. Kapetanovic García, Raúl Domínguez, J. Expósito, Laura González, Carla Marco, Julita Medina Castillo, Nuria Muelas, Daniel Natera‐de Benito, Nancy Carolina Ñungo Garzón, Inmaculada Pitarch Castellano, Teresa Sevilla, David Hervás
Được phát hành 2022Artigo -
2
Decoding the transcriptome of Duchenne muscular dystrophy to the single nuclei level reveals clinical-genetic correlations Bằng Xavier Suárez‐Calvet, Esther Fernández‐Simón, Daniel Natera‐de Benito, Cristina Jou, Patricia Piñol‐Jurado, Elisa Villalobos, C. Ortez, Alexandra Monceau, Marianela Schiava, Anna Codina, José Verdú-Díaz, James Clark, Zoe Laidler, Priyanka Mehra, Rasya Gokul-Nath, Jorge Alonso‐Pérez, Chiara Marini‐Bettolo, Giorgio Tasca, Volker Straub, Michela Guglieri, A. Nascimento, Jordi Díaz‐Manera
Được phát hành 2023Artigo -
3
Targeted Next-Generation Sequencing in a Large Cohort of Genetically Undiagnosed Patients with Neuromuscular Disorders in Spain Bằng Lídia González-Quereda, Maria José Rodríguez, Jordi Díaz‐Manera, Jorge Alonso‐Pérez, Eduard Gallardo, A. Nascimento, C. Ortez, Daniel Natera‐de Benito, Montse Olivé, Laura González, Adolfo López de Munaín, Miren Zulaica, Juan José Poza, Ivonne Jericó, Laura Torné, Pau Riera, José C. Milisenda, Aurora Sánchez, Glòria Garrabou, Isabel Llano‐Rivas, Marcos Madruga‐Garrido, P. Gallano
Được phát hành 2020Artigo -
4
Mutations of GEMIN5 are associated with coenzyme Q10 deficiency: long-term follow-up after treatment Bằng Marivi V. Cascajo-Almenara, Natalia Juliá‐Palacios, Roser Urreizti, Ana Sánchez‐Cuesta, Daniel J.M. Fernández‐Ayala, Elena García-Díaz, Clara Oliva, Maria del Mar O ́Callaghan, Abraham J. Paredes‐Fuentes, Pedro Moreno, Jordi Muchart, A. Nascimento, C. Ortez, Daniel Natera‐de Benito, M. Pineda, Noelia Rivera, Tyler R. Fortuna, Deepa Rajan, Plácido Navas, Leonardo Salviati, Francesc Palau, Dèlia Yubero, Àngels García‐Cazorla, Udai Bhan Pandey, Carlos Santos–Ocaña, Rafael Artuch
Được phát hành 2024Artigo -
5
Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes Bằng German Demidov, Steven Laurie, Annalaura Torella, Giulio Piluso, Marcello Scala, Manuela Morleo, Vincenzo Nigro, Holm Graeßner, Siddharth Banka, Alfons Macaya, Belén Pérez-Dueñas, Adam Jackson, Giovanni Stévanin, Jean‐Madeleine de Sainte Agathe, Markéta Havlovičová, Rita Horváth, Michele Pinelli, Nienke J.H. van Os, Bart P.C. van de Warrenburg, Anne‐Sophie Denommé‐Pichon, Marco Savarese, Mridul Johari, Bruno Dallapiccola, Marco Tartaglia, Martje G. Pauly, Anna Katharina Sommer, Tobias B. Haack, Ana Töpf, Didier Lacombe, Chiara Fallerini, Alessandra Renieri, Patrick F. Chinnery, Daniel Natera‐de Benito, A. Nascimento, Aurélien Trimouille, Francina Munell, Anna Marcé‐Grau, Ben Yaou Rabah, Gisèle Bonne, Liedewei Van de Vondel, Katja Lohmann, Stephan Ossowski
Được phát hành 2024Artigo -
6
The emerging spectrum of fetal acetylcholine receptor antibody-related disorders (FARAD) Bằng Nicholas M. Allen, Mark O’Rahelly, B. Eymard, Mondher Chouchane, Andreas Hahn, Gerry Kearns, Dae‐Seong Kim, Shin Yun Byun, Cam‐Tu Émilie Nguyen, Ulrike Schara‐Schmidt, Heike Kölbel, Adela Della Marina, Christiane Schneider‐Gold, Kathryn Roefke, Andrea Thieme, Peter Van den Bergh, G Avalos, Rodrigo Álvarez‐Velasco, Daniel Natera‐de Benito, Man Hin Mark Cheng, Wing Ki Chan, Hoi Shan Wan, Mary Ann Thomas, Lauren Borch, Julie Lauzon, Cornelia Kornblum, Jens Reimann, Andreas Mueller, Thierry Küntzer, Fiona Norwood, Sithara Ramdas, Leslie Jacobson, Xiaobo Jie, Miguel Ángel Fernández-García, Elizabeth Wraige, Ming Lim, Jean‐Pierre Lin, Kristl G. Claeys, Selma Aktaş, Maryam Oskoui, Yael Hacohen, A. Zaki Masud, Maria Isabel Leite, Jacqueline Palace, Darryl C. De Vivo, Angela Vincent, Heinz Jungbluth
Được phát hành 2023Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Medicine
Biology
Genetics
Gene
Internal medicine
Mutation
Disease
Endocrinology
Exome sequencing
Gene expression
Neuroscience
Pathology
Transcriptome
Acetylcholine receptor
Amyotrophic lateral sclerosis
Anatomy
Arthrogryposis
Arthrogryposis multiplex congenita
Bioinformatics
Cell biology
Coenzyme Q10
Cohort
Compound heterozygosity
Computational biology
Computer science
DNA sequencing
Downregulation and upregulation
Duchenne muscular dystrophy
Dystrophin
Environmental health