Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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Orphanet journal of rare diseases. - 14 (2019) , 199, ISSN: 1750-1172
- Keyword
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Myotonische Dystrophie
Registrierung
Kontrollierte klinische Studie
- Event
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Veröffentlichung
- (where)
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Freiburg
- (who)
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Universität
- (when)
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2019
- Creator
- DOI
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10.1186/s13023-019-1157-7
- URN
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urn:nbn:de:bsz:25-freidok-1510350
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:33 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Wood, Libby
- Lochmüller, Hanns
- Universität
Time of origin
- 2019
Other Objects (12)
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Disease burden of myotonic dystrophy type 1
Recommendations for improving the quality of rare disease registries
Health-related quality of life in patients with adult-onset myotonic dystrophy Type 1: a systematic review
Health-Related Quality of Life in Patients with Adult-Onset Myotonic Dystrophy Type 1: A Systematic Review
Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD)
Reproductive cancer risk factors in women with myotonic dystrophy (DM): survey data from the US and UK DM registries
Incomplete description of the current body of evidence of the health economics of Duchenne muscular dystrophy
The TREAT‐NMD DMD global database: analysis of more than 7,000 duchenne muscular dystrophy mutations
Analysis of the functional capacity outcome measures for myotonic dystrophy
Functional impairment in patients with myotonic dystrophy type 1 can be assessed by an ataxia rating scale (SARA)
Clinical outcomes in Duchenne Muscular Dystrophy: a study of 5345 patients from the TREAT-NMD DMD global database
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Disease burden of myotonic dystrophy type 1
Recommendations for improving the quality of rare disease registries
Health-related quality of life in patients with adult-onset myotonic dystrophy Type 1: a systematic review
Health-Related Quality of Life in Patients with Adult-Onset Myotonic Dystrophy Type 1: A Systematic Review
Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD)
Reproductive cancer risk factors in women with myotonic dystrophy (DM): survey data from the US and UK DM registries
Incomplete description of the current body of evidence of the health economics of Duchenne muscular dystrophy
The TREAT‐NMD DMD global database: analysis of more than 7,000 duchenne muscular dystrophy mutations
Analysis of the functional capacity outcome measures for myotonic dystrophy
Functional impairment in patients with myotonic dystrophy type 1 can be assessed by an ataxia rating scale (SARA)
Clinical outcomes in Duchenne Muscular Dystrophy: a study of 5345 patients from the TREAT-NMD DMD global database
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Disease burden of myotonic dystrophy type 1
Recommendations for improving the quality of rare disease registries
Health-related quality of life in patients with adult-onset myotonic dystrophy Type 1: a systematic review
Health-Related Quality of Life in Patients with Adult-Onset Myotonic Dystrophy Type 1: A Systematic Review
Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD)
Reproductive cancer risk factors in women with myotonic dystrophy (DM): survey data from the US and UK DM registries
Incomplete description of the current body of evidence of the health economics of Duchenne muscular dystrophy
The TREAT‐NMD DMD global database: analysis of more than 7,000 duchenne muscular dystrophy mutations
Analysis of the functional capacity outcome measures for myotonic dystrophy
Functional impairment in patients with myotonic dystrophy type 1 can be assessed by an ataxia rating scale (SARA)