- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD) ; volume:7 ; number:2 ; day:22 ; month:11 ; year:2012 ; pages:1-2 ; date:11.2012
Orphanet journal of rare diseases ; 7, Heft 2 (22.11.2012), 1-2, 11.2012
- Creator
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Rodger, Sunil
- Contributor
- DOI
-
10.1186/1750-1172-7-S2-A8
- URN
-
urn:nbn:de:1111-2016050121855
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:57 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
- Rodger, Sunil
- Steffensen, Birgit F.
- Lochmüller, Hanns
- SpringerLink (Online service)
Other Objects (12)
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Incomplete description of the current body of evidence of the health economics of Duchenne muscular dystrophy
Tumor necrosis factor receptor SF10A (TNFRSF10A) SNPs correlate with corticosteroid response in duchenne muscular dystrophy
Quantifying the burden of caregiving in Duchenne muscular dystrophy
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Economic Evaluation in Duchenne Muscular Dystrophy: Model Frameworks for Cost-Effectiveness Analysis
Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis
Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis
Adult care for Duchenne muscular dystrophy in the UK
Predictors of cardiac disease in duchenne muscular dystrophy: a systematic review and evidence grading
The TREAT‐NMD DMD global database: analysis of more than 7,000 duchenne muscular dystrophy mutations
Clinical outcomes in Duchenne Muscular Dystrophy: a study of 5345 patients from the TREAT-NMD DMD global database
Incomplete description of the current body of evidence of the health economics of Duchenne muscular dystrophy
Tumor necrosis factor receptor SF10A (TNFRSF10A) SNPs correlate with corticosteroid response in duchenne muscular dystrophy
Quantifying the burden of caregiving in Duchenne muscular dystrophy
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Economic Evaluation in Duchenne Muscular Dystrophy: Model Frameworks for Cost-Effectiveness Analysis
Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis
Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis
Adult care for Duchenne muscular dystrophy in the UK
Predictors of cardiac disease in duchenne muscular dystrophy: a systematic review and evidence grading
The TREAT‐NMD DMD global database: analysis of more than 7,000 duchenne muscular dystrophy mutations
Clinical outcomes in Duchenne Muscular Dystrophy: a study of 5345 patients from the TREAT-NMD DMD global database
Incomplete description of the current body of evidence of the health economics of Duchenne muscular dystrophy
Tumor necrosis factor receptor SF10A (TNFRSF10A) SNPs correlate with corticosteroid response in duchenne muscular dystrophy
Quantifying the burden of caregiving in Duchenne muscular dystrophy
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Economic Evaluation in Duchenne Muscular Dystrophy: Model Frameworks for Cost-Effectiveness Analysis
Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis
Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis
Adult care for Duchenne muscular dystrophy in the UK