Filters

David Metz, Anneke Grobler, Kate Carroll, Nisha Varma, Michael Kean, Anita Cairns, Katy de Valle, Ian R Woodcock, Eppie M Yiu, Zoe E Davidson, Martin B Delatycki, Nuran Dilek, Chad Heatwole, Monique M Ryan

Pharmacotherapy 2025;45(6):341-351

Free Full Text

Abstract

Can inhalation agents be used in the presence of a child with myopathy?

Francis Veyckemans

Current opinion in anaesthesiology 2010;23(3):348-55

Full Text

Abstract

Cross-sectional serum metabolomic study of multiple forms of muscular dystrophy.

Pietro Spitali, Kristina Hettne, Roula Tsonaka, Ekrem Sabir, Alexandre Seyer, Jesse B A Hemerik, Jelle J Goeman, Esther Picillo, Manuela Ergoli, Luisa Politano, Annemieke Aartsma-Rus

Journal of cellular and molecular medicine 2019;22(4):2442-2448

Free Full Text

Abstract

Safety and efficacy of a 6-month home-based exercise program in patients with facioscapulohumeral muscular dystrophy: A randomized controlled trial.

Landry-Cyrille Bankolé, Guillaume Y Millet, John Temesi, Damien Bachasson, Marion Ravelojaona, Bernard Wuyam, Samuel Verges, Elodie Ponsot, Jean-Christophe Antoine, Fawzi Kadi, Léonard Féasson

Medicine 2017;95(31):e4497

Free Full Text

Abstract

High-intensity interval training in facioscapulohumeral muscular dystrophy type 1: a randomized clinical trial.

Astrid Emile Buch, Karen Heje, John Vissing, Grete Andersen

Journal of neurology 2018;264(6):1099-1106

Full Text

Abstract

Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy. Report of two patients with and without 4q35 rearrangement.

A Uncini, G Galluzzi, A Di Muzio, M V De Angelis, E Ricci, C Scoppetta, S Servidei

Neuromuscular disorders : NMD 2003;12(9):874-7

Full Text

Abstract

Results: 1 – 15 / 19

Filters

Expert Opinion

Text Availability

Publication Types

Publication Year

Results for ""Muscular Dystrophy, Facioscapulohumeral""[mesh_terms]

Integrating clinical and genetic observations in facioscapulohumeral muscular dystrophy.

Late-onset myopathies.

Promising Perspective to Facioscapulohumeral Muscular Dystrophy Treatment: Nutraceuticals and Phytochemicals.

Drug treatment for facioscapulohumeral muscular dystrophy.

State-of-the-Art and Future Challenges for Nutritional Interventions in Facioscapulohumeral Dystrophy: A Narrative Review.

Indications for Tube Feeding in Adults with Muscular Disorders: A Scoping Review.

A pediatric case report and literature review of facioscapulohumeral muscular dystrophy type1.

Neuromuscular electrical stimulation training: a safe and effective treatment for facioscapulohumeral muscular dystrophy patients.

Aerobic training and postexercise protein in facioscapulohumeral muscular dystrophy: RCT study.

Effect of creatine monohydrate on motor function in children with facioscapulohumeral muscular dystrophy: A multicenter, randomized, double-blind placebo-controlled crossover trial.

Can inhalation agents be used in the presence of a child with myopathy?

Cross-sectional serum metabolomic study of multiple forms of muscular dystrophy.

Safety and efficacy of a 6-month home-based exercise program in patients with facioscapulohumeral muscular dystrophy: A randomized controlled trial.

High-intensity interval training in facioscapulohumeral muscular dystrophy type 1: a randomized clinical trial.

Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy. Report of two patients with and without 4q35 rearrangement.

Results for

""Muscular Dystrophy, Facioscapulohumeral""[mesh_terms]