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Adherence to treatment of primary osteoporosis and its association to fractures—the Swedish Adherence Register Analysis (SARA)

Osteoporosis international, 2012-02, Vol.23 (2), p.433-443

2012

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Quality of life of patients with spinal muscular atrophy: A systematic review

European journal of paediatric neurology, 2019-05, Vol.23 (3), p.347-356

2019

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A mini‐review and implementation model for using ataluren to treat nonsense mutation Duchenne muscular dystrophy

Acta Paediatrica, 2019-02, Vol.108 (2), p.224-230

2019

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The association between automatic generic substitution and treatment persistence with oral bisphosphonates

Osteoporosis international, 2012-08, Vol.23 (8), p.2201-2209

2012

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Clinical course of multiple sclerosis and labour‐force absenteeism: a longitudinal population‐based study

European journal of neurology, 2019-04, Vol.26 (4), p.603-609

2019

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Timing of Clinical Interventions in Patients With Duchenne Muscular Dystrophy: A Systematic Review and Grading of Evidence

Journal of Neuromuscular Diseases, 2022-01, Vol.9 (3), p.353-364

2022

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Residual effect after oral bisphosphonate treatment and healthy adherer effects—the Swedish adherence register analysis (SARA)

Osteoporosis international, 2015-01, Vol.26 (1), p.315-325

2015

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Predictors of Loss of Ambulation in Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis

Journal of Neuromuscular Diseases, 2024-04, Vol.11 (3), p.579-612

2024

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Factors Associated with Respiratory Health and Function in Duchenne Muscular Dystrophy: A Systematic Review and Evidence Grading

Journal of Neuromuscular Diseases, 2024-01, Vol.11 (1), p.25-57

2024

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Assessment of face validity of a disease model of nonsense mutation Duchenne muscular dystrophy: a multi-national Delphi panel study

Journal of medical economics, 2022, Vol.25 (1), p.808-816

2022

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Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis

European journal of epidemiology, 2020-07, Vol.35 (7), p.643-653

2020

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Consanguinity and autosomal recessive neuromuscular disorders

Developmental medicine and child neurology, 2016-08, Vol.58 (8), p.796-797

Landfeldt, Erik

2016

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Patient preferences for characteristics differentiating ovarian stimulation treatments

Human reproduction (Oxford), 2012-03, Vol.27 (3), p.760-769

2012

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Duchenne muscular dystrophy and caregiver burden: a systematic review

Developmental medicine and child neurology, 2018-10, Vol.60 (10), p.987-996

2018

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CO79 Predictors of Outcomes Measured after Loss of Ambulation in Duchenne Muscular Dystrophy: A Literature Review and Grading of the Evidence

Value in health, 2022-07, Vol.25 (7), p.S318

2022

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MSR21 Cost-Effectiveness Analysis of Treatments for Nonsense Mutation Duchenne Muscular Dystrophy: Expert Validation of Model Face Validity

Value in health, 2022-07, Vol.25 (7), p.S521-S522

2022

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HPR68 Timing of Initiation of Clinical Interventions in Patients with Duchenne Muscular Dystrophy: A Systematic Review and Grading of the Evidence

Value in health, 2022-07, Vol.25 (7), p.S478-S479

2022

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Extending Life in Duchenne Muscular Dystrophy: Implications for Appraisals of Cost-Effectiveness

PharmacoEconomics - open, 2019-09, Vol.3 (3), p.279-280

Landfeldt, Erik

2019

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Economic Costs of Myasthenia Gravis: A Systematic Review

PharmacoEconomics, 2020-07, Vol.38 (7), p.715-728

2020

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REGISTRIES, CARE, QUALITY OF LIFE, MANAGEMENT OF NMD

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S146-S147

2020

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REGISTRIES, CARE, QUALITY OF LIFE, MANAGEMENT OF NMD: P.345 Rasch analysis of the pediatric quality of life inventory 4.0 generic core scales administered to patients with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S146-S147

2020

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What Relapsed/Refractory Cll/Mcl Treatment Outcomes Do German Patients And Physicians Find Most Important? Results from Qualitative Interviews

Value in health, 2014-11, Vol.17 (7), p.A650-A650

2014

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G.O.14

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.853-853

2014

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Improvements in health status and utility associated with ataluren for the treatment of nonsense mutation Duchenne muscular dystrophy

Muscle & nerve, 2020-03, Vol.61 (3), p.363-368

2020

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Quantifying the burden of caregiving in Duchenne muscular dystrophy

Journal of neurology, 2016-05, Vol.263 (5), p.906-915

2016

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Adherence to treatment of primary osteoporosis and its association to fractures—the Swedish Adherence Register Analysis (SARA)

Quality of life of patients with spinal muscular atrophy: A systematic review

A mini‐review and implementation model for using ataluren to treat nonsense mutation Duchenne muscular dystrophy

The association between automatic generic substitution and treatment persistence with oral bisphosphonates

Clinical course of multiple sclerosis and labour‐force absenteeism: a longitudinal population‐based study

Timing of Clinical Interventions in Patients With Duchenne Muscular Dystrophy: A Systematic Review and Grading of Evidence

Residual effect after oral bisphosphonate treatment and healthy adherer effects—the Swedish adherence register analysis (SARA)

Predictors of Loss of Ambulation in Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis

Factors Associated with Respiratory Health and Function in Duchenne Muscular Dystrophy: A Systematic Review and Evidence Grading

Assessment of face validity of a disease model of nonsense mutation Duchenne muscular dystrophy: a multi-national Delphi panel study

Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis

Consanguinity and autosomal recessive neuromuscular disorders

Patient preferences for characteristics differentiating ovarian stimulation treatments

Duchenne muscular dystrophy and caregiver burden: a systematic review

CO79 Predictors of Outcomes Measured after Loss of Ambulation in Duchenne Muscular Dystrophy: A Literature Review and Grading of the Evidence

MSR21 Cost-Effectiveness Analysis of Treatments for Nonsense Mutation Duchenne Muscular Dystrophy: Expert Validation of Model Face Validity

HPR68 Timing of Initiation of Clinical Interventions in Patients with Duchenne Muscular Dystrophy: A Systematic Review and Grading of the Evidence

Extending Life in Duchenne Muscular Dystrophy: Implications for Appraisals of Cost-Effectiveness

Economic Costs of Myasthenia Gravis: A Systematic Review

REGISTRIES, CARE, QUALITY OF LIFE, MANAGEMENT OF NMD

REGISTRIES, CARE, QUALITY OF LIFE, MANAGEMENT OF NMD: P.345 Rasch analysis of the pediatric quality of life inventory 4.0 generic core scales administered to patients with Duchenne muscular dystrophy

What Relapsed/Refractory Cll/Mcl Treatment Outcomes Do German Patients And Physicians Find Most Important? Results from Qualitative Interviews

G.O.14

Improvements in health status and utility associated with ataluren for the treatment of nonsense mutation Duchenne muscular dystrophy

Quantifying the burden of caregiving in Duchenne muscular dystrophy

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