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Can simple and low-cost motor function assessments help in the diagnostic suspicion of Duchenne muscular dystrophy?
J Pediatr (Rio J). 2020 Jul-Aug;96(4):503-510. doi: 10.1016/j.jped.2019.02.003. Epub 2019 Apr 19.
2
Steroid treatment and the development of scoliosis in males with duchenne muscular dystrophy.
J Bone Joint Surg Am. 2004 Mar;86(3):519-24. doi: 10.2106/00004623-200403000-00009.
4
Glucocorticoid corticosteroids for Duchenne muscular dystrophy.
Cochrane Database Syst Rev. 2008 Jan 23(1):CD003725. doi: 10.1002/14651858.CD003725.pub3.
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Progression of muscular co-activation and gait variability in children with Duchenne muscular dystrophy: A 2-year follow-up study.
Clin Biomech (Bristol). 2020 Aug;78:105101. doi: 10.1016/j.clinbiomech.2020.105101. Epub 2020 Jul 3.
6
Glucocorticoid corticosteroids for Duchenne muscular dystrophy.
Cochrane Database Syst Rev. 2004(2):CD003725. doi: 10.1002/14651858.CD003725.pub2.
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Natural History of Steroid-Treated Young Boys With Duchenne Muscular Dystrophy Using the NSAA, 100m, and Timed Functional Tests.
Pediatr Neurol. 2020 Dec;113:15-20. doi: 10.1016/j.pediatrneurol.2020.08.013. Epub 2020 Aug 27.
10
Strong correlation between the 6-minute walk test and accelerometry functional outcomes in boys with Duchenne muscular dystrophy.
J Child Neurol. 2015 Mar;30(3):357-63. doi: 10.1177/0883073814530502. Epub 2014 Apr 23.

引用本文的文献

1
Detecting early signs in Duchenne muscular dystrophy: comprehensive review and diagnostic implications.
Front Pediatr. 2023 Nov 10;11:1276144. doi: 10.3389/fped.2023.1276144. eCollection 2023.

本文引用的文献

1
Consensus on the diagnosis, treatment and follow-up of patients with Duchenne muscular dystrophy.
Neurologia (Engl Ed). 2019 Sep;34(7):469-481. doi: 10.1016/j.nrl.2018.01.001. Epub 2018 Mar 9.
4
Genetic modifiers of Duchenne and facioscapulohumeral muscular dystrophies.
Muscle Nerve. 2018 Jan;57(1):6-15. doi: 10.1002/mus.25953. Epub 2017 Sep 22.
5
Brazilian consensus on Duchenne muscular dystrophy. Part 1: diagnosis, steroid therapy and perspectives.
Arq Neuropsiquiatr. 2017 Aug;75(8):104-113. doi: 10.1590/0004-282x20170112.
6
Developing a Natural History Progression Model for Duchenne Muscular Dystrophy Using the Six-Minute Walk Test.
CPT Pharmacometrics Syst Pharmacol. 2017 Sep;6(9):596-603. doi: 10.1002/psp4.12220. Epub 2017 Aug 29.
7
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements.
Neuromuscul Disord. 2017 May;27(5):447-451. doi: 10.1016/j.nmd.2017.02.006. Epub 2017 Feb 14.
8
Timed Rise from Floor as a Predictor of Disease Progression in Duchenne Muscular Dystrophy: An Observational Study.
PLoS One. 2016 Mar 16;11(3):e0151445. doi: 10.1371/journal.pone.0151445. eCollection 2016.
9
Timed motor function tests capacity in healthy children.
Arch Dis Child. 2016 Feb;101(2):147-51. doi: 10.1136/archdischild-2014-307396. Epub 2015 Nov 13.
10
Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36-month changes.
PLoS One. 2014 Oct 1;9(10):e108205. doi: 10.1371/journal.pone.0108205. eCollection 2014.

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