Detalles de la búsqueda
1.
Cross-sectorial collaboration on policy-driven rehabilitation care models for persons with neuromuscular diseases: reflections and behavior of community-based health professionals.
BMC Health Serv Res
; 22(1): 1168, 2022 Sep 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-36114488
2.
Congenital Titinopathy: Comprehensive characterization and pathogenic insights.
Ann Neurol
; 83(6): 1105-1124, 2018 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-29691892
3.
Collagen XII myopathy with rectus femoris atrophy and collagen XII retention in fibroblasts.
Muscle Nerve
; 57(6): 1026-1030, 2018 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-29342313
4.
Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy.
Brain
; 139(Pt 3): 674-91, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26700687
5.
Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations.
Muscle Nerve
; 53(3): 388-93, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26172852
6.
Fatigue in patients with spinal muscular atrophy type II and congenital myopathies: evaluation of the fatigue severity scale.
Qual Life Res
; 23(5): 1479-88, 2014 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-24214178
7.
Burden of Disease of Duchenne Muscular Dystrophy in Denmark - A National Register-Based Study of Individuals with Duchenne Muscular Dystrophy and their Closest Relatives.
J Neuromuscul Dis
; 11(2): 443-457, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38217608
8.
Cross-sectoral collaboration among hospital professionals on rehabilitation for patients with neuromuscular diseases.
Neurodegener Dis Manag
; 13(3): 161-175, 2023 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-36994773
9.
People with neuromuscular diseases and their relatives' perspectives on challenges in everyday life and healthcare.
Neurodegener Dis Manag
; 13(5): 289-302, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-38078426
10.
A retrospective study of needs and interventions among patients with myotonic dystrophy type 1 in Denmark referred to rehabilitation in the period 2000-2019.
J Eval Clin Pract
; 29(1): 39-48, 2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-35615973
11.
Development of an International SMA Bulbar Assessment for Inter-professional Administration.
J Neuromuscul Dis
; 10(4): 639-652, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37212069
12.
Participation amongst people ageing with neuromuscular disease: a qualitative study of lived experiences.
Nurs Open
; 9(6): 2675-2682, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34165266
13.
Investigating job satisfaction in palliative rehabilitation: Reflections and perspectives of health professionals working with amyotrophic lateral sclerosis.
J Eval Clin Pract
; 28(1): 108-119, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34269500
14.
Ageing with neuromuscular disease: getting lost in transitions.
Disabil Rehabil
; 44(16): 4311-4318, 2022 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-33761303
15.
Perspectives on Everyday Life Challenges of Danish Young People With Duchenne Muscular Dystrophy (DMD) on Corticosteroids.
Glob Qual Nurs Res
; 9: 23333936221094858, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35493771
16.
Parents' advice to other parents of children with spinal muscular atrophy: Two nationwide follow-ups.
J Child Health Care
; 26(3): 407-421, 2022 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-33998314
17.
[Early diagnosis of spinal muscular atrophy].
Ugeskr Laeger
; 183(51)2021 12 20.
Artículo
en Danés
| MEDLINE | ID: mdl-34981731
18.
Impact of the COVID-19 pandemic on biopsychosocial health and quality of life among Danish children and adults with neuromuscular diseases (NMD)-Patient reported outcomes from a national survey.
PLoS One
; 16(6): e0253715, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34191825
19.
Progression or Not - A Small Natural History Study of Genetical Confirmed Congenital Myopathies.
J Neuromuscul Dis
; 8(4): 647-655, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33646172
20.
Parents' Experiences of Information and Decision Making in the Care of Their Child With Severe Spinal Muscular Atrophy: A Population Survey.
J Child Neurol
; 34(4): 210-215, 2019 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-30642225