- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1432-1459
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Disease burden of myotonic dystrophy type 1 ; volume:266 ; number:4 ; day:20 ; month:2 ; year:2019 ; pages:998-1006 ; date:4.2019
Journal of neurology ; 266, Heft 4 (20.2.2019), 998-1006, 4.2019
- Urheber
-
Landfeldt, Erik
Nikolenko, Nikoletta
Jimenez-Moreno, Cecilia
Cumming, Sarah
Monckton, Darren G.
Gorman, Grainne
Turner, Chris
Lochmüller, Hanns
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1007/s00415-019-09228-w
- URN
-
urn:nbn:de:101:1-2019040822083121915884
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:52 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Landfeldt, Erik
- Nikolenko, Nikoletta
- Jimenez-Moreno, Cecilia
- Cumming, Sarah
- Monckton, Darren G.
- Gorman, Grainne
- Turner, Chris
- Lochmüller, Hanns
- SpringerLink (Online service)
Ähnliche Objekte (12)
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
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
Functional impairment in patients with myotonic dystrophy type 1 can be assessed by an ataxia rating scale (SARA)
Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD)
Change over time in ability to perform activities of daily living in myotonic dystrophy type 1
Change over time in ability to perform activities of daily living in myotonic dystrophy type 1
Associations between variant repeat interruptions and clinical outcomes in myotonic dystrophy type 1
Quantifying the burden of caregiving in Duchenne muscular dystrophy
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
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
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
Functional impairment in patients with myotonic dystrophy type 1 can be assessed by an ataxia rating scale (SARA)
Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD)
Change over time in ability to perform activities of daily living in myotonic dystrophy type 1
Change over time in ability to perform activities of daily living in myotonic dystrophy type 1
Associations between variant repeat interruptions and clinical outcomes in myotonic dystrophy type 1
Quantifying the burden of caregiving in Duchenne muscular dystrophy
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
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
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
Functional impairment in patients with myotonic dystrophy type 1 can be assessed by an ataxia rating scale (SARA)
Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD)
Change over time in ability to perform activities of daily living in myotonic dystrophy type 1
Change over time in ability to perform activities of daily living in myotonic dystrophy type 1
Associations between variant repeat interruptions and clinical outcomes in myotonic dystrophy type 1
Quantifying the burden of caregiving in Duchenne muscular dystrophy
Incomplete description of the current body of evidence of the health economics of Duchenne muscular dystrophy