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BMJ OPEN (2017)
Quality of life in 188 patients with myasthenia gravis in China
Yongxiang Yang et al.
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Asger Frost et al.
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Sarah Hoffmann et al.
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An up-date on health-related quality of life in myasthenia gravis -results from population based cohorts
M. I. Boldingh et al.
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Clinical features and impact of myasthenia gravis disease in Australian patients
Stefan Blum et al.
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Stephanie Ohlraun et al.
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The Chalder Fatigue Scale (CFQ 11)
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Myasthenia gravis epidemiology in a national cohort; combining multiple disease registries
J. B. Andersen et al.
ACTA NEUROLOGICA SCANDINAVICA (2014)
HEALTH-RELATED QUALITY-OF-LIFE AND TREATMENT TARGETS IN MYASTHENIA GRAVIS
Kimiaki Utsugisawa et al.
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The impact of rheumatoid arthritis on quality-of-life assessed using the SF-36: A systematic review and meta-analysis
Faith Matcham et al.
SEMINARS IN ARTHRITIS AND RHEUMATISM (2014)
Measurement of socioeconomic status in the German health interview and examination survey for adults (DEGS1)
T. Lampert et al.
BUNDESGESUNDHEITSBLATT-GESUNDHEITSFORSCHUNG-GESUNDHEITSSCHUTZ (2013)
The first wave of the German Health Interview and Examination Survey for Adults (DEGS1). Sample design, response, weighting, and representativeness
P. Kamtsiuris et al.
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Elena Hernandez Martinez De Lapiscina et al.
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Ivana Z. Basta et al.
NEUROLOGICAL SCIENCES (2012)
A German adaption of the ENRICHD Social Support Inventory: statistical results in patients with heart disease
Friederike Kendel et al.
DIAGNOSTICA (2011)
Quality of life and life circumstances in German myasthenia gravis patients
Sabine Twork et al.
HEALTH AND QUALITY OF LIFE OUTCOMES (2010)
Concordance between severity of disease, disability and health-related quality of life in Myasthenia gravis
Alberto Raggi et al.
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The assessment of chronic fatigue: psychometric properties of the Fatigue Scale (FS)
Alexandra Martin et al.
ZEITSCHRIFT FUR KLINISCHE PSYCHOLOGIE UND PSYCHOTHERAPIE (2010)
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Anne Taraldsen Heldal et al.
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Martina Krokavcova et al.
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Less is more, or almost as much: A 15-item quality-of-life instrument for myasthenia gravis
Ted M. Burns et al.
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Health value, perceived social support, and health self-efficacy as factors in a health-promoting lifestyle
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A Riazi et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2003)
The validity of the Hospital Anxiety and Depression Scale - An updated literature review
I Bjelland et al.
JOURNAL OF PSYCHOSOMATIC RESEARCH (2002)
Quality of life in patients with myasthenia gravis
L Padua et al.
MUSCLE & NERVE (2002)
Health-related quality of life in patients with myasthenia gravis and the relationship between patient-oriented assessment and conventional measurements
L Padua et al.
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RH Paul et al.
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