Literature DB >> 34355124

Management of motor rehabilitation in individuals with muscular dystrophies. 1st Consensus Conference report from UILDM - Italian Muscular Dystrophy Association (Rome, January 25-26, 2019).

Maria Elena Lombardo1, Elena Carraro2, Cristina Sancricca1,3, Michela Armando4, Michela Catteruccia5, Elena Mazzone6, Giulia Ricci7, Ferdinando Salamino8, Filippo Maria Santorelli9, Massimiliano Filosto10.   

Abstract

Muscular dystrophy (MD) is a group of neuromuscular diseases characterized by progressive muscle weakness due to various mutations in several genes involved in muscle structure and function. The age at onset, evolution and severity of the different forms of MD can vary and there is often impairment of motor function and activities of daily living. Although there have been important scientific advances with regard to pharmacological therapies for many forms of MD, rehabilitation management remains central to ensuring the patient's psychophysical well-being. Here we report the results of an Italian consensus conference promoted by UILDM (Unione Italiana Lotta alla Distrofia Muscolare, the Italian Muscular Dystrophy Association) in order to establish general indications and agreed protocols for motor rehabilitation of the different forms of MD. ©2021 Gaetano Conte Academy - Mediterranean Society of Myology, Naples, Italy.

Entities:  

Keywords:  exercise; muscular dystrophy; rehabilitation

Mesh:

Year:  2021        PMID: 34355124      PMCID: PMC8290512          DOI: 10.36185/2532-1900-046

Source DB:  PubMed          Journal:  Acta Myol        ISSN: 1128-2460


  79 in total

1.  Resistance training in patients with limb-girdle and becker muscular dystrophies.

Authors:  Marie-Louise Sveen; Søren P Andersen; Lina H Ingelsrud; Sarah Blichter; Niels E Olsen; Simon Jønck; Thomas O Krag; John Vissing
Journal:  Muscle Nerve       Date:  2012-11-21       Impact factor: 3.217

Review 2.  Strength training and aerobic exercise training for muscle disease.

Authors:  Nicoline Bm Voet; Elly L van der Kooi; Baziel Gm van Engelen; Alexander Ch Geurts
Journal:  Cochrane Database Syst Rev       Date:  2019-12-06

3.  Evidence-based guideline summary: Evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine.

Authors:  Rabi Tawil; John T Kissel; Chad Heatwole; Shree Pandya; Gary Gronseth; Michael Benatar
Journal:  Neurology       Date:  2015-07-28       Impact factor: 9.910

4.  Validation of the ICF core set for neuromuscular diseases.

Authors:  I Bos; H A Stallinga; B Middel; J B M Kuks; K Wynia
Journal:  Eur J Phys Rehabil Med       Date:  2012-11-21       Impact factor: 2.874

5.  Cognitive behavioural therapy with optional graded exercise therapy in patients with severe fatigue with myotonic dystrophy type 1: a multicentre, single-blind, randomised trial.

Authors:  Kees Okkersen; Cecilia Jimenez-Moreno; Stephan Wenninger; Ferroudja Daidj; Jeffrey Glennon; Sarah Cumming; Roberta Littleford; Darren G Monckton; Hanns Lochmüller; Michael Catt; Catharina G Faber; Adrian Hapca; Peter T Donnan; Gráinne Gorman; Guillaume Bassez; Benedikt Schoser; Hans Knoop; Shaun Treweek; Baziel G M van Engelen
Journal:  Lancet Neurol       Date:  2018-06-19       Impact factor: 44.182

Review 6.  Consensus statement on standard of care for congenital muscular dystrophies.

Authors:  Ching H Wang; Carsten G Bonnemann; Anne Rutkowski; Thomas Sejersen; Jonathan Bellini; Vanessa Battista; Julaine M Florence; Ulrike Schara; Pamela M Schuler; Karim Wahbi; Annie Aloysius; Robert O Bash; Christophe Béroud; Enrico Bertini; Kate Bushby; Ronald D Cohn; Anne M Connolly; Nicolas Deconinck; Isabelle Desguerre; Michelle Eagle; Brigitte Estournet-Mathiaud; Ana Ferreiro; Albert Fujak; Nathalie Goemans; Susan T Iannaccone; Patricia Jouinot; Marion Main; Paola Melacini; Wolfgang Mueller-Felber; Francesco Muntoni; Leslie L Nelson; Jes Rahbek; Susana Quijano-Roy; Caroline Sewry; Kari Storhaug; Anita Simonds; Brian Tseng; Jiri Vajsar; Andrea Vianello; Reinhard Zeller
Journal:  J Child Neurol       Date:  2010-11-15       Impact factor: 1.987

7.  Dysferlinopathy course and sportive activity: clues for possible treatment.

Authors:  C Angelini; E Peterle; A Gaiani; L Bortolussi; C Borsato
Journal:  Acta Myol       Date:  2011-10

8.  The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boys.

Authors:  Marika Pane; Elena Stacy Mazzone; Serena Sivo; Lavinia Fanelli; Roberto De Sanctis; Adele D'Amico; Sonia Messina; Roberta Battini; Flaviana Bianco; Marianna Scutifero; Roberta Petillo; Silvia Frosini; Roberta Scalise; Gian Luca Vita; Claudio Bruno; Marina Pedemonte; Tiziana Mongini; Elena Pegoraro; Francesca Brustia; Alice Gardani; Angela Berardinelli; Valentina Lanzillotta; Emanuela Viggiano; Filippo Cavallaro; Maria Sframeli; Luca Bello; Andrea Barp; Fabio Busato; Serena Bonfiglio; Enrica Rolle; Giulia Colia; Annamaria Bonetti; Concetta Palermo; Alessandra Graziano; Grazia D'Angelo; Antonella Pini; Alice Corlatti; Ksenija Gorni; Giovanni Baranello; Laura Antonaci; Enrico Bertini; Luisa Politano; Eugenio Mercuri
Journal:  PLoS Curr       Date:  2014-10-07

Review 9.  Neuromuscular Diseases and Bone.

Authors:  Giovanni Iolascon; Marco Paoletta; Sara Liguori; Claudio Curci; Antimo Moretti
Journal:  Front Endocrinol (Lausanne)       Date:  2019-11-22       Impact factor: 5.555

Review 10.  Efficacy of muscle exercise in patients with muscular dystrophy: a systematic review showing a missed opportunity to improve outcomes.

Authors:  Silvia Gianola; Valentina Pecoraro; Simone Lambiase; Roberto Gatti; Giuseppe Banfi; Lorenzo Moja
Journal:  PLoS One       Date:  2013-06-12       Impact factor: 3.240

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