Quality of instruments assessing activity and participation of people with muscular dystrophy: A systematic review of participant‐reported outcome measures-Reference-Cited by-同舟云学术

Quality of instruments assessing activity and participation of people with muscular dystrophy: A systematic review of participant‐reported outcome measures

Published:2022-07-21 Issue:12 Volume:64 Page:1453-1461
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:Develop Med Child Neuro

Author:

Andrade Keysy K. S.¹^ORCID,Soares Luana A.¹^ORCID,Macedo Caik C.¹^ORCID,Bispo Nelcilaine R.¹^ORCID,Sousa Junior Ricardo R.²^ORCID,Oliveira Vinícius C.¹^ORCID,Leite Hércules R.¹²^ORCID,Gaiad Thaís P.¹^ORCID

Affiliation:

1. Department of Physical Therapy, Faculty of Health Sciences Universidade Federal dos Vales do Jequitinhonha e Mucuri Diamantina Minas Gerais Brazil

2. School of Physical Education, Physiotherapy and Occupational Therapy Universidade Federal de Minas Gerais Belo Horizonte Minas Gerais Brazil

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/dmcn.15345

Reference71 articles.

1. The Epidemiology of Neuromuscular Diseases

2. A Fisioterapia na Amiotrofia Espinhal Progressiva Tipo I;Jorge MGAV;Revista Neurociências.,2013

3. Motor Measures: A Moving Target?

4. Physical Therapy for Children‐E‐Book;Palisano RJ;Elsevier Health Sciences,2014

5. Doenças neuromusculares e instrumentos úteis na avaliação motora em crianças e adolescentes;Diniz GPC;Rev Med Minas Gerais.,2010

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