Responsiveness to Change of 5-point MRC scale, Endurance and Functional Evaluation for Assessing Myositis in Daily Clinical Practice.
暂无分享,去创建一个
Y. Allenbach | O. Benveniste | O. Landon-Cardinal | Olivier Benveniste | H. Devilliers | Océane Landon-Cardinal | Hervé Devilliers | Nathalie Chavarot | Kuberaka Mariampillai | Aude Rigolet | Baptiste Hervier | Yves Allenbach | B. Hervier | K. Mariampillai | A. Rigolet | N. Chavarot
[1] A. Mammen,et al. Muscle endurance deficits in myositis patients despite normal manual muscle testing scores , 2018, Muscle & nerve.
[2] A. Mammen,et al. 224th ENMC International Workshop: Clinico-sero-pathological classification of immune-mediated necrotizing myopathies Zandvoort, The Netherlands, 14–16 October 2016 , 2017, Neuromuscular Disorders.
[3] J. Hogrel,et al. Physical activity monitoring: A promising outcome measure in idiopathic inflammatory myopathies , 2017, Neurology.
[4] S. Paganoni,et al. Outcome measures in the idiopathic inflammatory myopathies , 2017, Neurology.
[5] W. Stenzel,et al. Advances in serological diagnostics of inflammatory myopathies. , 2016, Current opinion in neurology.
[6] Oakley,et al. 213th ENMC International Workshop: Outcome measures and clinical trial readiness in idiopathic inflammatory myopathies, Heemskerk, The Netherlands, 18–20 September 2015 , 2016, Neuromuscular Disorders.
[7] K. Wadell,et al. Correlation between Limb Muscle Endurance, Strength, and Functional Capacity in People with Chronic Obstructive Pulmonary Disease , 2016, Physiotherapy Canada. Physiotherapie Canada.
[8] L. Servais,et al. Four-year longitudinal study of clinical and functional endpoints in sporadic inclusion body myositis: Implications for therapeutic trials , 2014, Neuromuscular Disorders.
[9] T. Voit,et al. Innovative methods to assess upper limb strength and function in non-ambulant Duchenne patients , 2013, Neuromuscular Disorders.
[10] Alan Tennant,et al. Modifying the Medical Research Council grading system through Rasch analyses , 2011, Brain : a journal of neurology.
[11] David Hilton-Jones,et al. Long-term observational study of sporadic inclusion body myositis. , 2011, Brain : a journal of neurology.
[12] B. Feldman,et al. Validation of manual muscle testing and a subset of eight muscles for adult and juvenile idiopathic inflammatory myopathies , 2010, Arthritis care & research.
[13] D. Koziol,et al. Distribution and severity of weakness among patients with polymyositis, dermatomyositis and juvenile dermatomyositis. , 2009, Rheumatology.
[14] I. Lundberg,et al. Functional index-2: Validity and reliability of a disease-specific measure of impairment in patients with polymyositis and dermatomyositis. , 2006, Arthritis and rheumatism.
[15] I. Targoff,et al. Novel Classification of Idiopathic Inflammatory Myopathies Based on Overlap Syndrome Features and Autoantibodies: Analysis of 100 French Canadian Patients , 2005, Medicine.
[16] A. Windebank,et al. History of standard scoring, notation, and summation of neuromuscular signs. A current survey and recommendation , 2005, Journal of the peripheral nervous system : JPNS.
[17] R. Hughes,et al. 119th ENMC international workshop: Trial design in adult idiopathic inflammatory myopathies, with the exception of inclusion body myositis, 10–12 October 2003, Naarden, The Netherlands , 2004, Neuromuscular Disorders.
[18] W. Kuis,et al. Preliminary core sets of measures for disease activity and damage assessment in juvenile systemic lupus erythematosus and juvenile dermatomyositis. , 2003, Rheumatology.
[19] S. Chevret,et al. Standards of Measurements in Myasthenia Gravis , 2003, Annals of the New York Academy of Sciences.
[20] P. Lachenbruch,et al. Defining Clinical Improvement in Adult and Juvenile Myositis. , 2003, The Journal of rheumatology.
[21] G. Huberfeld,et al. Validity and reliability of two muscle strength scores commonly used as endpoints in assessing treatment of myasthenia gravis , 2000, Journal of Neurology.
[22] L. Pachman,et al. Development of validated disease activity and damage indices for the juvenile idiopathic inflammatory myopathies. II. The Childhood Myositis Assessment Scale (CMAS): a quantitative tool for the evaluation of muscle function. The Juvenile Dermatomyositis Disease Activity Collaborative Study Group. , 1999, Arthritis and rheumatism.
[23] J Drukker,et al. Quadriceps strength and timed motor performances in myotonic dystrophy, Charcot–Marie–Tooth disease, and healthy subjects , 1998, Clinical rehabilitation.
[24] S. Dimauro,et al. Inclusion body myositis and myopathies , 1995, Annals of neurology.
[25] F. P. Kendall,et al. Muscles, testing and function , 1971 .
[26] April. AIDS TO THE INVESTIGATION OF PERIPHERAL NERVE INJURIES , 1943 .