OpenAlex Citation Counts

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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

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

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

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

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

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

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

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

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

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

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

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

Telerehabilitation Methods in Pediatric Rehabilitation
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

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

Asymptomatic HyperCKemia in the Pediatric Population
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

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