Chronic pain in neuromuscular disease: pain site and intensity differentially impacts function.
暂无分享,去创建一个
[1] C. Desnuelle,et al. Pain assessment in Charcot-Marie-Tooth (CMT) disease. , 2012, Annals of physical and rehabilitation medicine.
[2] H. Kautiainen,et al. Pain in patients with myotonic dystrophy type 2: A postal survey in finland , 2012, Muscle & nerve.
[3] K. Raichle,et al. Changes in Pain-related Beliefs, Coping, and Catastrophizing Predict Changes in Pain Intensity, Pain Interference, and Psychological Functioning in Individuals With Myotonic Muscular Dystrophy and Facioscapulohumeral Dystrophy , 2012, The Clinical journal of pain.
[4] D. Ehde,et al. Psychosocial factors and adjustment to chronic pain in persons with physical disabilities: a systematic review. , 2011, Archives of physical medicine and rehabilitation.
[5] Daniel G. Miller,et al. Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene , 2010, PLoS genetics.
[6] Massimiliano Valeriani,et al. Mechanisms of neuropathic pain in patients with Charcot-Marie-Tooth 1 A: A laser-evoked potential study , 2010, PAIN®.
[7] M. Jensen,et al. Psychosocial Factors and Adjustment to Pain in Individuals with Postpolio Syndrome , 2010, American journal of physical medicine & rehabilitation.
[8] Jau-Shin Lou,et al. Assessment and Management of Fatigue in Neuromuscular Disease , 2010, The American journal of hospice & palliative care.
[9] M. Jensen,et al. Pain in Youths With Neuromuscular Disease , 2009, The American journal of hospice & palliative care.
[10] Jay J. Han,et al. Rehabilitation Management of Neuromuscular Disease: The Role of Exercise Training , 2009, Journal of clinical neuromuscular disease.
[11] K. Raichle,et al. Impact of Biopsychosocial Factors on Chronic Pain in Persons With Myotonic and Facioscapulohumeral Muscular Dystrophy , 2009, The American journal of hospice & palliative care.
[12] B. Natvig,et al. Does the number of musculoskeletal pain sites predict work disability? A 14‐year prospective study , 2009, European journal of pain.
[13] I. Molton,et al. Coping With Chronic Pain Among Younger, Middle-Aged, and Older Adults Living With Neurological Injury and Disease , 2008, Journal of aging and health.
[14] R. Abresch,et al. Pain in myotonic muscular dystrophy, type 1. , 2008, Archives of physical medicine and rehabilitation.
[15] R. Abresch,et al. Pain in persons with postpolio syndrome: frequency, intensity, and impact. , 2008, Archives of physical medicine and rehabilitation.
[16] K. Dunn,et al. Chronic pain reconsidered , 2008, PAIN.
[17] B. Natvig,et al. Localized or widespread musculoskeletal pain: Does it matter? , 2008, PAIN.
[18] A. Quattrone,et al. Charcot-Marie-Tooth and pain: correlations with neurophysiological, clinical, and disability findings , 2008, Neurological Sciences.
[19] R. Abresch,et al. Chronic pain in persons with myotonic dystrophy and facioscapulohumeral dystrophy. , 2008, Archives of physical medicine and rehabilitation.
[20] F. Boureau,et al. Pain in hereditary neuromuscular disorders and myasthenia gravis: a national survey of frequency, characteristics, and impact. , 2008, Journal of pain and symptom management.
[21] C. Schmidt,et al. Simple patterns behind complex spatial pain reporting? Assessing a classification of multisite pain reporting in the general population , 2007, PAIN®.
[22] A. Breen,et al. Chronic musculoskeletal pain rarely presents in a single body site: results from a UK population study. , 2007, Rheumatology.
[23] Suzanne G. Leveille,et al. The pathway from musculoskeletal pain to mobility difficulty in older disabled women , 2007, Pain.
[24] J. Turner,et al. Mediators, moderators, and predictors of therapeutic change in cognitive–behavioral therapy for chronic pain , 2007, PAIN.
[25] A. Thevenon,et al. Pain and Neuromuscular Disease: The Results of a Survey , 2006, American journal of physical medicine & rehabilitation.
[26] P. Leino-Arjas,et al. Pain and health related functioning among employees , 2006, Journal of Epidemiology and Community Health.
[27] J. Engel,et al. Exploring chronic pain in youths with Duchenne Muscular Dystrophy: a model for pediatric neuromuscular disease. , 2005, Physical medicine and rehabilitation clinics of North America.
[28] R. Abresch,et al. Chronic pain in persons with neuromuscular disease. , 2005, Physical medicine and rehabilitation clinics of North America.
[29] M. Zwarts,et al. Experienced fatigue in facioscapulohumeral dystrophy, myotonic dystrophy, and HMSN-I , 2005, Journal of Neurology, Neurosurgery & Psychiatry.
[30] R. Abresch,et al. Chronic pain in persons with neuromuscular disease. , 2005, Archives of physical medicine and rehabilitation.
[31] B. Natvig,et al. Low back pain as a predictor of long-term work disability , 2002, Scandinavian journal of public health.
[32] K. Campbell,et al. Pain site and impairment in individuals with amputation pain. , 2002, Archives of physical medicine and rehabilitation.
[33] R. Abresch,et al. Assessment of pain and health-related quality of life in slowly progressive neuromuscular disease , 2002, The American journal of hospice & palliative care.
[34] R. Abresch,et al. Health-related quality of life in peripheral neuropathy. , 2001, Physical medicine and rehabilitation clinics of North America.
[35] K. Bushby,et al. Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reports , 1998, Neuromuscular Disorders.
[36] T D Bird,et al. Neuropathic pain in Charcot-Marie-Tooth disease. , 1998, Archives of physical medicine and rehabilitation.
[37] C. Stohler,et al. Greater disability with increased pain involvement, pain intensity and depressive preoccupation , 1997, European journal of pain.
[38] R. Abresch,et al. Profiles of neuromuscular diseases. Facioscapulohumeral muscular dystrophy. , 1995, American journal of physical medicine & rehabilitation.
[39] W. Verhagen,et al. The auditory, vestibular, and oculomotor system in facioscapulohumeral dystrophy. , 1995, Acta oto-laryngologica. Supplementum.
[40] W. Reardon,et al. Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. , 1993, American journal of human genetics.
[41] C. Caskey,et al. Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring. , 1993, JAMA.
[42] L. Surh,et al. The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy. , 1992, Journal of medical genetics.
[43] E. Boerwinkle,et al. Anticipation in myotonic dystrophy , 1992, Neurology.
[44] A. Emery. Population frequencies of inherited neuromuscular diseases—A world survey , 1991, Neuromuscular Disorders.
[45] J. D. Mann,et al. Relationship of pain drawing scores to ratings of pain description and function. , 1991, The Clinical journal of pain.
[46] P. Harper,et al. DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease , 1990, The Lancet.
[47] J. Weber,et al. Location of facioscapulohumeral muscular dystrophy gene on chromosome 4 , 1990, The Lancet.
[48] R. B. Margolis,et al. Pain extent: relations with psychological state, pain severity, pain history, and disability , 1990, Pain.
[49] A. Zuckerman,et al. Letter: Heterologous stimulation of hepatitis-B antigen. , 1974, The Lancet.