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Cited by 1,167

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management

Open access
Birnkrant, David J, Bushby, Katharine, Bann, Carla M, Alman, Benjamin A, Apkon, Susan D, Blackwell, Angela, Case, Laura E, Cripe, Linda, Hadjiyannakis, Stasia, Olson, Aaron K, Sheehan, Daniel W, Bolen, Julie, Weber, David R, Ward, Leanne M·2018·The Lancet Neurology

Abstract

A coordinated, multidisciplinary approach to care is essential for optimum management of the primary manifestations and secondary complications of Duchenne muscular dystrophy (DMD). Contemporary care has been shaped by the availability of more sensitive diagnostic techniques and the earlier use of therapeutic interventions, which have the potential to improve patients’ duration and quality of life. In part 2 of this update of the DMD care considerations, we present the latest recommendations for respiratory, cardiac, bone health and osteoporosis, and orthopaedic and surgical management for boys and men with DMD. Additionally, we provide guidance on cardiac management for female carriers of a disease-causing mutation. The new care considerations acknowledge the effects of long-term glucocorticoid use on the natural history of DMD, and the need for care guidance across the lifespan as patients live longer. The management of DMD looks set to change substantially as new genetic and molecular therapies become available.

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Metadata

Authors
Birnkrant, D. J., Bushby, K., Bann, C. M., Alman, B. A., Apkon, S. D., Blackwell, A., Case, L. E., Cripe, L., Hadjiyannakis, S., Olson, A. K., Sheehan, D. W., Bolen, J., Weber, D. R., & Ward, L. M.
Venue
The Lancet Neurology
Publisher
Elsevier BV
Published
2018-04
Volume
17
Issue
4
Pages
347-361
ISSN
1474-4422 (ISSN-L)
OpenAlex
W2784812244
Cited by
1,167
References
2
FWCI
32.25
Type
journal article
Language
en
Open access
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CoChat. (2026). Citation check: Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management. https://app.cochat.ai/papers/10.1016/s1474-4422(18)30025-5
The paper
Birnkrant, D. J., Bushby, K., Bann, C. M., Alman, B. A., Apkon, S. D., Blackwell, A., Case, L. E., Cripe, L., Hadjiyannakis, S., Olson, A. K., Sheehan, D. W., Bolen, J., Weber, D. R., & Ward, L. M. (2018). Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management. The Lancet Neurology. https://doi.org/10.1016/s1474-4422(18)30025-5

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.