
OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Consenso para el diagnóstico, tratamiento y seguimiento del paciente con distrofia muscular de Duchenne
A. Nascimento Osorio, Jordi Cantillo, Ana Camacho, et al.
Neurología (2018) Vol. 34, Iss. 7, pp. 469-481
Open Access | Times Cited: 33
A. Nascimento Osorio, Jordi Cantillo, Ana Camacho, et al.
Neurología (2018) Vol. 34, Iss. 7, pp. 469-481
Open Access | Times Cited: 33
Showing 1-25 of 33 citing articles:
Pubertal induction therapy in pediatric patients with Duchenne muscular dystrophy
Giorgio Sodero, Clelia Cipolla, Donato Rigante, et al.
Journal of Pediatric Endocrinology and Metabolism (2025)
Closed Access | Times Cited: 1
Giorgio Sodero, Clelia Cipolla, Donato Rigante, et al.
Journal of Pediatric Endocrinology and Metabolism (2025)
Closed Access | Times Cited: 1
The Value of Genetic Counseling in Duchenne Muscular Dystrophy: An Example of a Personal Case Series
Youssra Loukhmas, Imane Chahid, Ahmed Aziz Bousfiha
World Journal of Neuroscience (2025) Vol. 15, Iss. 01, pp. 73-83
Open Access
Youssra Loukhmas, Imane Chahid, Ahmed Aziz Bousfiha
World Journal of Neuroscience (2025) Vol. 15, Iss. 01, pp. 73-83
Open Access
Optimized efficient screening for Duchenne muscular dystrophy carriers using proto-oncogene tyrosine-protein kinase receptor Ret
Dongyang Hong, Zhilei Zhang, Yun Sun, et al.
Laboratory Medicine (2025)
Closed Access
Dongyang Hong, Zhilei Zhang, Yun Sun, et al.
Laboratory Medicine (2025)
Closed Access
Clinical practice guidelines for the diagnosis and management of Duchenne muscular dystrophy: a scoping review
Marco Málaga, Aarón Rodríguez-Calienes, Fabian A. Chavez‐Ecos, et al.
Frontiers in Neurology (2024) Vol. 14
Open Access | Times Cited: 3
Marco Málaga, Aarón Rodríguez-Calienes, Fabian A. Chavez‐Ecos, et al.
Frontiers in Neurology (2024) Vol. 14
Open Access | Times Cited: 3
Nanomedicine for Gene Delivery and Drug Repurposing in the Treatment of Muscular Dystrophies
Ilaria Andreana, Mathieu Repellin, Flavia Carton, et al.
Pharmaceutics (2021) Vol. 13, Iss. 2, pp. 278-278
Open Access | Times Cited: 21
Ilaria Andreana, Mathieu Repellin, Flavia Carton, et al.
Pharmaceutics (2021) Vol. 13, Iss. 2, pp. 278-278
Open Access | Times Cited: 21
Longitudinal study of multi-parameter quantitative magnetic resonance imaging in Duchenne muscular dystrophy: hyperresponsiveness of gluteus maximus and detection of subclinical disease progression in functionally stable patients
Fei Peng, Huayan Xu, Yu Song, et al.
Journal of Neurology (2022) Vol. 270, Iss. 3, pp. 1439-1451
Closed Access | Times Cited: 10
Fei Peng, Huayan Xu, Yu Song, et al.
Journal of Neurology (2022) Vol. 270, Iss. 3, pp. 1439-1451
Closed Access | Times Cited: 10
Utilization of T1-Mapping for the pelvic and thigh muscles in Duchenne Muscular Dystrophy: a quantitative biomarker for disease involvement and correlation with clinical assessments
Fei Peng, Huayan Xu, Yu Song, et al.
BMC Musculoskeletal Disorders (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 9
Fei Peng, Huayan Xu, Yu Song, et al.
BMC Musculoskeletal Disorders (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 9
Effectiveness of a 5-Week Virtual Reality Telerehabilitation Program for Children With Duchenne and Becker Muscular Dystrophy: Prospective Quasi-Experimental Study
María Rosa Baeza-Barragán, María Teresa Labajos Manzanares, Mercedes Cristina Amaya-Álvarez, et al.
JMIR Serious Games (2023) Vol. 11, pp. e48022-e48022
Open Access | Times Cited: 5
María Rosa Baeza-Barragán, María Teresa Labajos Manzanares, Mercedes Cristina Amaya-Álvarez, et al.
JMIR Serious Games (2023) Vol. 11, pp. e48022-e48022
Open Access | Times Cited: 5
A qualitative exploration of the priorities and experiences of children with Duchenne muscular dystrophy, their parents, and healthcare professionals around weight management
Meaghan Walker, Bhavnita Mistry, Reshma Amin, et al.
Disability and Rehabilitation (2021) Vol. 44, Iss. 26, pp. 8234-8242
Closed Access | Times Cited: 11
Meaghan Walker, Bhavnita Mistry, Reshma Amin, et al.
Disability and Rehabilitation (2021) Vol. 44, Iss. 26, pp. 8234-8242
Closed Access | Times Cited: 11
Physiotherapeutic Interventions for Patients With Rare Genetic Muscle-Wasting Disorders: A Systematic Review and Meta-Analysis
Abdullah Alzahrani
Cureus (2024)
Open Access | Times Cited: 1
Abdullah Alzahrani
Cureus (2024)
Open Access | Times Cited: 1
Assessing the value of delandistrogene moxeparvovec (SRP-9001) gene therapy in patients with Duchenne muscular dystrophy in the United States
Alexa C. Klimchak, Lauren E. Sedita, Louise R. Rodino‐Klapac, et al.
Journal of Market Access & Health Policy (2023) Vol. 11, Iss. 1
Open Access | Times Cited: 3
Alexa C. Klimchak, Lauren E. Sedita, Louise R. Rodino‐Klapac, et al.
Journal of Market Access & Health Policy (2023) Vol. 11, Iss. 1
Open Access | Times Cited: 3
Confirmatory validation of the french version of the Duchenne Muscular Dystrophy module of the pediatric quality of life inventory (PedsQLTM3.0DMDfv)
Elisabeth Wallach, Virginie Ehlinger, Maëlle Biotteau, et al.
BMC Pediatrics (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 2
Elisabeth Wallach, Virginie Ehlinger, Maëlle Biotteau, et al.
BMC Pediatrics (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 2
Analysis of Long Noncoding RNAs-Related Regulatory Mechanisms in Duchenne Muscular Dystrophy Using a Disease-Related lncRNA-mRNA Pathway Network
Bing Xu, Chunlei Zheng
Genetics Research (2022) Vol. 2022, pp. 1-15
Open Access | Times Cited: 4
Bing Xu, Chunlei Zheng
Genetics Research (2022) Vol. 2022, pp. 1-15
Open Access | Times Cited: 4
Consenso colombiano para el seguimiento de pacientes con Distrofia muscular de Duchenne
Maritza Muñoz Rivas, Sandra Milena Castellar-Leones, Edicson Ruiz Ospina, et al.
Pediatría (2020) Vol. 52, Iss. 3, pp. 75-84
Open Access | Times Cited: 5
Maritza Muñoz Rivas, Sandra Milena Castellar-Leones, Edicson Ruiz Ospina, et al.
Pediatría (2020) Vol. 52, Iss. 3, pp. 75-84
Open Access | Times Cited: 5
Can simple and low-cost motor function assessments help in the diagnostic suspicion of Duchenne muscular dystrophy?
Aline Chacon Pereira, Alexandra Prufer de Queiroz Campos Araújo, Márcia Gonçalves Ribeiro
Jornal de Pediatria (2019) Vol. 96, Iss. 4, pp. 503-510
Open Access | Times Cited: 4
Aline Chacon Pereira, Alexandra Prufer de Queiroz Campos Araújo, Márcia Gonçalves Ribeiro
Jornal de Pediatria (2019) Vol. 96, Iss. 4, pp. 503-510
Open Access | Times Cited: 4
Asymmetric Myocardial Involvement as an Early Indicator of Cardiac Dysfunction in Pediatric Dystrophinopathies: A Study on Cardiac Magnetic Resonance (CMR) Parametric Mappings
Roger Esmel-Vilomara, Lucía Riaza, Laura Costa-Comellas, et al.
Pediatric Cardiology (2024) Vol. 46, Iss. 3, pp. 685-693
Open Access
Roger Esmel-Vilomara, Lucía Riaza, Laura Costa-Comellas, et al.
Pediatric Cardiology (2024) Vol. 46, Iss. 3, pp. 685-693
Open Access
Long-term course of gastrostomy nutritional management in patients with Duchenne muscular dystrophy: A retrospective cohort study
Yuki Takanarita, Yuichi Okata, Hiroyuki Awano, et al.
Journal of Clinical Neuroscience (2024) Vol. 129, pp. 110857-110857
Closed Access
Yuki Takanarita, Yuichi Okata, Hiroyuki Awano, et al.
Journal of Clinical Neuroscience (2024) Vol. 129, pp. 110857-110857
Closed Access
Telerehabilitation Methods in Pediatric Rehabilitation
N. N. Uzun
TELe-Health (2024), pp. 109-122
Closed Access
N. N. Uzun
TELe-Health (2024), pp. 109-122
Closed Access
An Exoskeleton Design and Numerical Characterization for Children with Duchenne Muscular Dystrophy
Cristian Copiluși, Sorin Dumitru, Nicolae Dumitru, et al.
Bioengineering (2024) Vol. 11, Iss. 11, pp. 1072-1072
Open Access
Cristian Copiluși, Sorin Dumitru, Nicolae Dumitru, et al.
Bioengineering (2024) Vol. 11, Iss. 11, pp. 1072-1072
Open Access
Characterization of Nonclinical Drug Metabolism and Pharmacokinetic Properties of Phosphorodiamidate Morpholino Oligonucleotides, A Novel Drug Class for Duchenne Muscular Dystrophy
Andrew K.L. Goey, Marie Claire Mukashyaka, Yogesh T. Patel, et al.
Drug Metabolism and Disposition (2024) Vol. 52, Iss. 12, pp. 1396-1406
Open Access
Andrew K.L. Goey, Marie Claire Mukashyaka, Yogesh T. Patel, et al.
Drug Metabolism and Disposition (2024) Vol. 52, Iss. 12, pp. 1396-1406
Open Access
Caregiver Global Impression Observations from EMBARK: A Phase 3 Study Evaluating Delandistrogene Moxeparvovec in Ambulatory Patients with Duchenne Muscular Dystrophy
Craig M. McDonald, Jacob Elkins, Sai Dharmarajan, et al.
Neurology and Therapy (2024)
Open Access
Craig M. McDonald, Jacob Elkins, Sai Dharmarajan, et al.
Neurology and Therapy (2024)
Open Access
Research hotspots and trends for Duchenne muscular dystrophy: a machine learning bibliometric analysis from 2004 to 2023
Pingping Fang, Jingzhe Han, Di An, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access
Pingping Fang, Jingzhe Han, Di An, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access
Asymptomatic HyperCKemia in the Pediatric Population
Pilar Martí, Inmaculada Pitarch Castellano, Nuria Muelas, et al.
Neurology (2024) Vol. 104, Iss. 1
Closed Access
Pilar Martí, Inmaculada Pitarch Castellano, Nuria Muelas, et al.
Neurology (2024) Vol. 104, Iss. 1
Closed Access
Early assessment of cardiomyopathy in Duchenne patients by means of longitudinal strain echocardiography
Marcos Clavero Adell, A. Ayerza Casas, Daniel Palanca Arias, et al.
Cardiology in the Young (2023) Vol. 34, Iss. 1, pp. 151-156
Open Access | Times Cited: 1
Marcos Clavero Adell, A. Ayerza Casas, Daniel Palanca Arias, et al.
Cardiology in the Young (2023) Vol. 34, Iss. 1, pp. 151-156
Open Access | Times Cited: 1