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Validation of The Individualized Neuromuscular Quality of Life in Japanese patients with myotonic dystrophy
Fujino H, Saito T, Takahashi MP, et al.
Muscle & Nerve, 2018
What explains high life satisfaction in men living with Duchenne Muscular Dystrophy? A preliminary study to inform psychological intervention
Graham CD, Rose MR
Muscle & Nerve, 2017, 56, 1, p 163
Interventions for dysphagia in long-term, progressive muscle disease
Jones K, Pitceathly RD, Rose MR, et al.
Cochrane Database of Systematic Reviews, 2016, 2
Treatment for inclusion body myositis
Rose MR, Jones K, Leong K, et al.
Cochrane Database of Systematic Reviews, 2015, 6
Activity rating scales in adult muscle disease : what do they actually measure?
Seedat F, James MK, Rose MR
Muscle & Nerve, 2014, 50, 1, p. 14-23
188th ENMC International Workshop : Inclusion Body Myositis, 2-4 December 2011, Naarden, The Netherlands
Collectif, ENMC IBM Working Group, Rose MR
Neuromuscular disorders : NMD, 2013, 23, 12, p. 1044-1055
Quality of life and measures of quality of life in patients with neuromuscular disorders
Burns TM, Graham CD, Rose MR, et al.
Muscle & Nerve, 2012, 46, 1, p. 9-25
Scapular fixation in muscular dystrophy
Orrell RW, Copeland S, Rose MR
Cochrane Database of Systematic Reviews, 2010, 1, CD003278, p. 1-14
Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases
Sansone VA, Panzeri M, Montanari M, et al.
European journal of neurology, 2010, 17, 9, p. 1178-1187
What determines quality of life in inclusion body myositis ?
Sadjadi R, Rose MR, The Muscle Study Group
Journal of neurology, neurosurgery and psychiatry, 2010, 81, 10, p. 1164-1166
Drug treatment for facioscapulohumeral muscular dystrophy
Rose MR, Tawil R
Cochrane Database of Systematic Reviews, 2008, 4, CD002276, p. 1-19
Measuring and understanding quality of life in adult muscle disease
Rose MR
Congrès : Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France)
2008, p. 71
Qualité de vie dans la maladie neuromusculaire. Measuring and understanding quality of life in adult muscle disease
Rose MR
Congrès : 5e Congrès international de rééducation dans les maladies neuromusculaires (5th international rehabilitation conference in neuromuscular diseases; 30 mai - 1er juin 2008; Marseille, France)
2008, p. 8
Construction and validation of a quality of life questionnaire for neuromuscular disease (INQoL)
Vincent KA, Carr AJ, Walburn J, et al.
Neurology, 2007, 68, 13, p. 1051-1057
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
Zhou H, Jungbluth H, Sewry CA, et al.
Brain, 2007, 130, 8, p. 2024-2036
Inclusion body myositis
Mastaglia FL, Hilton-Jones D, Rose MR, et al.
Handbook of Clinical Neurology (Myopathie), 2007, 86, 3rd series, cha, p. 255-272, p. 13
Charcot-Marie-Tooth disease impairs quality of life. Why ? And how do we improve it ?
Shy ME, Rose MR
Neurology, 2005, 65, 6, p. 790-791
119th ENMC international workshop : Trial design in adult idiopathic inflammatory myopathies, with the exception of inclusion body myositis
Collectif, Amato AA, Lecky BRF, et al.
Neuromuscular disorders : NMD, 2004, 14, 5, p. 337-345
A prospective natural history study of inclusion body myositis : Implications for clinical trials
Rose MR, McDermott MP, Thornton CA, et al.
Neurology, 2001, 57, p. 548-550
The dropped head plus syndrome : Quantitation of response to corticosteroids
Rose MR, Levin KH, Griggs RC
Muscle & Nerve, 1999, 22, 1, p. 115-118
A case of myopathy associated with a dystrophin gene deletion and abnormal glycogen storage.
Rose MR, Howard JF, Genet SA, et al.
Muscle & Nerve, 1993, 16, 1, p. 57-62
A rapidly progressive adolescent-onset oculopharyngeal somatic syndrome with rimmed vacuoles in two siblings
Rose MR, Landon DN, Papadimitriou A, et al.
Annals of neurology, 01/97, 41, p. 25-31
