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Editorial
. 2022 Aug;66(2):116-117.
doi: 10.1002/mus.27574. Epub 2022 Jun 6.

Age at diagnosis for Duchenne muscular dystrophy: Why we must do better

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Editorial

Age at diagnosis for Duchenne muscular dystrophy: Why we must do better

Rosaline Mary Quinlivan. Muscle Nerve. 2022 Aug.
No abstract available

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References

REFERENCES

    1. Thomas S, Conway K, Fapo O, et al. Time to diagnosis of Duchenne Muscular Dystrophy remains unchanged: findings from the muscular dystrophy surveillance, tracking and research network (MDSTARnet) 2000-2015. Muscle Nerve. 2022;66:193-197.
    1. Bushby K, Finkel R, Birnkrant DJ, et al. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol. 2010;9:77-93.
    1. Eagle M, Baudouin S, Chandler C, Giddings DR, Bullock R, Bushby K. Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation. Neuromuscul Disord. 2002;12:926-929.
    1. Birnkrant DJ, Bushby K, Bann CM, et al. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management. Lancet Neurol. 2018;17:251-267.
    1. Ricotti V, Ridout D, Scott E, et al. Long-term benefits and adverse effects of intermittent versus daily glucocorticoids in boys with Duchenne muscular dystrophy. J Neurol Neurosurg Psychiatry. 2013;84:698-705.

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