Found: 30
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Understanding the Perseverance of the Muscular Dystrophy Community One-Year into the COVID-19 Pandemic.
- Published in:
- Journal of Neuromuscular Diseases, 2022, v. 9, n. 4, p. 517, doi. 10.3233/JND-220794
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- Article
Validation of the Italian version of the Charcot‐Marie‐Tooth Health Index.
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- Journal of the Peripheral Nervous System, 2020, v. 25, n. 3, p. 292, doi. 10.1111/jns.12397
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- Article
Disease Burden in Children With Spinal Muscular Atrophy: Results From a Large Cross-Sectional Study.
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- Journal of Child Neurology, 2023, v. 38, n. 1/2, p. 52, doi. 10.1177/08830738221135918
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- Article
Quantitative Foot Muscle Magnetic Resonance Imaging Reliably Measures Disease Progression in Children and Adolescents with Charcot–Marie–Tooth Disease Type 1A.
- Published in:
- Annals of Neurology, 2024, v. 96, n. 1, p. 170, doi. 10.1002/ana.26934
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- Article
The Charcot-Marie-Tooth Health Index: Evaluation of a Patient-Reported Outcome.
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- 2018
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- journal article
Lower limb muscle MRI fat fraction is a responsive outcome measure in CMT X1, 1B and 2A.
- Published in:
- Annals of Clinical & Translational Neurology, 2024, v. 11, n. 3, p. 607, doi. 10.1002/acn3.51979
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- Article
Patient-reported impact of symptoms in adrenoleukodystrophy (PRISM-ALD).
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- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03129-6
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- Article
Patient-Reported Impact of Symptoms in Fibromyalgia (PRISM-FM).
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- Journal of Rheumatology, 2024, v. 51, n. 6, p. 628, doi. 10.3899/jrheum.2023-0698
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- Article
Assessing Prevalence and Characteristics of Oro-bulbar Involvement in Children and Adults with SMA Type 2 and 3 Using a Multimodal Approach.
- Published in:
- Dysphagia (0179051X), 2023, v. 38, n. 6, p. 1568, doi. 10.1007/s00455-023-10584-z
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- Article
Patient‐ and caregiver‐reported impact of symptoms in Duchenne muscular dystrophy.
- Published in:
- Muscle & Nerve, 2024, v. 70, n. 1, p. 120, doi. 10.1002/mus.28102
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- Article
A longitudinal study of disease progression in facioscapulohumeral muscular dystrophy (FSHD).
- Published in:
- Muscle & Nerve, 2024, v. 69, n. 3, p. 362, doi. 10.1002/mus.28031
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- Article
The Facioscapulohumeral Muscular Dystrophy‐Health Index: Development and evaluation of a disease‐specific outcome measure.
- Published in:
- Muscle & Nerve, 2023, v. 68, n. 4, p. 422, doi. 10.1002/mus.27951
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- Article
Assessing perspectives of disease burden and clinically meaningful changes using the Spinal Muscular Atrophy Health Index in adolescents and young adults.
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- Muscle & Nerve, 2022, v. 66, n. 3, p. 276, doi. 10.1002/mus.27644
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- Article
A patient‐focused survey to assess the effects of the COVID‐19 pandemic and social guidelines on people with muscular dystrophy.
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- Muscle & Nerve, 2021, v. 64, n. 3, p. 321, doi. 10.1002/mus.27349
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- Article
The Spinal Muscular Atrophy Health Index: A novel outcome for measuring how a patient feels and functions.
- Published in:
- 2021
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- Publication type:
- journal article
Electrical impedance myography in facioscapulohumeral muscular dystrophy: A 1-year follow-up study.
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- 2018
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- Publication type:
- journal article
Facioscapulohumeral muscular dystrophy functional composite outcome measure.
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- 2018
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- Publication type:
- journal article
Myotonic dystrophy patient preferences in patient-reported outcome measures.
- Published in:
- 2018
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- Publication type:
- journal article
Electrical impedance myography in facioscapulohumeral muscular dystrophy.
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- 2016
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- Publication type:
- journal article
Myotonic dystrophy health index: Correlations with clinical tests and patient function.
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- 2016
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- Publication type:
- journal article
Prospective study of muscle cramps in Charcot-Marie-Tooth disease.
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- Muscle & Nerve, 2015, v. 51, n. 4, p. 485, doi. 10.1002/mus.24333
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- Article
Myotonic Dystrophy Health Index: Initial evaluation of a disease-specific outcome measure.
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- Muscle & Nerve, 2014, v. 49, n. 6, p. 906, doi. 10.1002/mus.24097
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- Article
Visualization of the diaphragm muscle with ultrasound improves diagnostic accuracy of phrenic nerve conduction studies.
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- Muscle & Nerve, 2014, v. 49, n. 5, p. 669, doi. 10.1002/mus.24059
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- Publication type:
- Article
Evoked myotonia can be "dialed-up" by increasing stimulus train length in myotonic dystrophy type 1.
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- 2010
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- Publication type:
- journal article
Evoked myotonia can be 'dialed-up' by increasing stimulus train length in myotonic dystrophy type 1.
- Published in:
- Muscle & Nerve, 2010, v. 41, n. 2, p. 191, doi. 10.1002/mus.21481
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- Article
Computerized hand grip myometry reliably measures myotonia and muscle strength in myotonic dystrophy (DM1).
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- Muscle & Nerve, 2007, v. 36, n. 3, p. 320, doi. 10.1002/mus.20822
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- Article
Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy.
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- Muscle & Nerve, 2007, v. 35, n. 4, p. 479, doi. 10.1002/mus.20722
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- Article
Development and validation of a caregiver‐reported outcome measure for Alzheimer's disease: the Alzheimer's Disease Caregiver Reported‐Health Index (ADCR‐HI), a fully validated tool to bolster clinical trial and research infrastructure.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, n. 21, p. 1, doi. 10.1002/alz.077303
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- Article
Development of a patient‐reported outcome measure for Alzheimer's disease: the Alzheimer's Disease‐Health Index (AD‐HI), a fully validated tool to bolster clinical trial and research infrastructure.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, n. 21, p. 1, doi. 10.1002/alz.077264
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- Article
The Alzheimer's Disease‐Health Indices (AD‐HI): Development of Two Novel Outcome Measures for Use in Clinical Trials.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 7, p. 1, doi. 10.1002/alz.068858
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- Article