6.
Bos I, Stallinga H, Middel B, Kuks J, Wynia K
. Validation of the ICF core set for neuromuscular diseases. Eur J Phys Rehabil Med. 2012; 49(2):179-87.
View
7.
Voet N, van der Kooi E, van Engelen B, Geurts A
. Strength training and aerobic exercise training for muscle disease. Cochrane Database Syst Rev. 2019; 12:CD003907.
PMC: 6953420.
DOI: 10.1002/14651858.CD003907.pub5.
View
8.
Iolascon G, Paoletta M, Liguori S, Curci C, Moretti A
. Neuromuscular Diseases and Bone. Front Endocrinol (Lausanne). 2019; 10:794.
PMC: 6886381.
DOI: 10.3389/fendo.2019.00794.
View
9.
Sveen M, Andersen S, Ingelsrud L, Blichter S, Olsen N, Jonck S
. Resistance training in patients with limb-girdle and becker muscular dystrophies. Muscle Nerve. 2012; 47(2):163-9.
DOI: 10.1002/mus.23491.
View
10.
Pane M, Mazzone E, Sivo S, Fanelli L, de Sanctis R, DAmico A
. The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boys. PLoS Curr. 2015; 6.
PMC: 4208936.
DOI: 10.1371/currents.md.a93d9904d57dcb08936f2ea89bca6fe6.
View
11.
Angelini C, Peterle E, Gaiani A, Bortolussi L, Borsato C
. Dysferlinopathy course and sportive activity: clues for possible treatment. Acta Myol. 2011; 30(2):127-32.
PMC: 3235880.
View
12.
Ferreira M, Sherrington C, Smith K, Carswell P, Bell R, Bell M
. Physical activity improves strength, balance and endurance in adults aged 40-65 years: a systematic review. J Physiother. 2012; 58(3):145-56.
DOI: 10.1016/S1836-9553(12)70105-4.
View
13.
Orngreen M, Olsen D, Vissing J
. Aerobic training in patients with myotonic dystrophy type 1. Ann Neurol. 2005; 57(5):754-7.
DOI: 10.1002/ana.20460.
View
14.
Fagoaga J, Girabent-Farres M, Bagur-Calafat C, Febrer A, Steffensen B
. [Functional assessment for people unable to walk due to spinal muscular atrophy and Duchenne muscular dystrophy. Translation and validation of the Egen Klassifikation 2 scale for the Spanish population]. Rev Neurol. 2015; 60(10):439-46.
View
15.
Cudia P, Weis L, Baba A, Kiper P, Marcante A, Rossi S
. Effects of Functional Electrical Stimulation Lower Extremity Training in Myotonic Dystrophy Type I: A Pilot Controlled Study. Am J Phys Med Rehabil. 2016; 95(11):809-817.
DOI: 10.1097/PHM.0000000000000497.
View
16.
Anziska Y, Inan S
. Exercise in neuromuscular disease. Semin Neurol. 2014; 34(5):542-56.
DOI: 10.1055/s-0034-1396008.
View
17.
Gagnon C, Heatwole C, Hebert L, Hogrel J, Laberge L, Leone M
. Report of the third outcome measures in myotonic dystrophy type 1 (OMMYD-3) international workshop Paris, France, June 8, 2015. J Neuromuscul Dis. 2018; 5(4):523-537.
DOI: 10.3233/JND-180329.
View
18.
Vissing C, Preisler N, Husu E, Prahm K, Vissing J
. Aerobic training in patients with anoctamin 5 myopathy and hyperckemia. Muscle Nerve. 2014; 50(1):119-23.
DOI: 10.1002/mus.24112.
View
19.
Birnkrant D, Bushby K, Bann C, Apkon S, Blackwell A, Brumbaugh D
. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management. Lancet Neurol. 2018; 17(3):251-267.
PMC: 5869704.
DOI: 10.1016/S1474-4422(18)30024-3.
View
20.
Lexell J, Brogardh C
. The use of ICF in the neurorehabilitation process. NeuroRehabilitation. 2014; 36(1):5-9.
DOI: 10.3233/NRE-141184.
View