| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adult North Star Network (ANSN): Consensus Guideline For The Standard Of Care Of Adults With Duchenne Muscular Dystrophy
|
Quinlivan, R.
|
|
|
8 |
6 |
p. 899-926
|
artikel
|
| 2 |
Clinical Outcome Evaluations and CBT Response Prediction in Myotonic Dystrophy
|
van As, Daniël
|
|
|
8 |
6 |
p. 1031-1046
|
artikel
|
| 3 |
Compliance to DMD Care Considerations in the Netherlands
|
Heutinck, Lotte
|
|
|
8 |
6 |
p. 927-938
|
artikel
|
| 4 |
Coping in Children and Adolescents with a Genetic Muscle Disorder –Findings from a Population-Based Study
|
Jones, Kelly M.
|
|
|
8 |
6 |
p. 1069-1078
|
artikel
|
| 5 |
COVID-19 in a Cohort of Patients with Congenital Myasthenic Syndrome
|
Alabaf, Setareh
|
|
|
8 |
6 |
p. 1003-1005
|
artikel
|
| 6 |
Diffusion Tensor Imaging Shows Differences Between Myotonic Dystrophy Type 1 and Type 2
|
Rehmann, R.
|
|
|
8 |
6 |
p. 949-962
|
artikel
|
| 7 |
Emerging Oligonucleotide Therapeutics for Rare Neuromuscular Diseases
|
Aoki, Yoshitsugu
|
|
|
8 |
6 |
p. 869-884
|
artikel
|
| 8 |
Estimation of the Quality-of-Life Impact of X-Linked Myotubular Myopathy
|
Lloyd, Andrew
|
|
|
8 |
6 |
p. 1047-1061
|
artikel
|
| 9 |
Have Duchenne Muscular Dystrophy Patients an Increased Cancer Risk?
|
Vita, Gian Luca
|
|
|
8 |
6 |
p. 1063-1067
|
artikel
|
| 10 |
Healthcare Utilisation and Satisfaction with Care in Patients with Amyotrophic Lateral Sclerosis - An Observational Study
|
Kierkegaard, Marie
|
|
|
8 |
6 |
p. 1079-1088
|
artikel
|
| 11 |
How Patient Organizations Can Drive FAIR Data Efforts to Facilitate Research and Health Care: A Report of the Virtual Second International Meeting on Duchenne Data Sharing, March 3, 2021
|
van Lin, Nawel
|
|
|
8 |
6 |
p. 1097-1108
|
artikel
|
| 12 |
Inflammatory Myositis Secondary to Anti-Retroviral Therapy in a Child; Case Report and Review of the Literature
|
Monaghan, Marie
|
|
|
8 |
6 |
p. 1089-1095
|
artikel
|
| 13 |
Multifocal Noninvasive Magnetic Stimulation of the Primary Motor Cortex in Type 1 Myotonic Dystrophy –A Proof of Concept Pilot Study
|
Greene, Ericka
|
|
|
8 |
6 |
p. 963-972
|
artikel
|
| 14 |
Open-Label Evaluation of Eteplirsen in Patients with Duchenne Muscular Dystrophy Amenable to Exon 51 Skipping: PROMOVI Trial
|
McDonald, Craig M.
|
|
|
8 |
6 |
p. 989-1001
|
artikel
|
| 15 |
Quantitative Evaluation of Upright Posture by x-Ray and 3D Stereophotogrammetry with a New Marker Set Protocol in Late Onset Pompe Disease
|
De Blasiis, Paolo
|
|
|
8 |
6 |
p. 979-988
|
artikel
|
| 16 |
Subcutaneous Immunoglobulin Therapy with IgPro20 in Patients with Stiff Person Syndrome and Primary Immunodeficiency Disease
|
Francis, Olivia L.
|
|
|
8 |
6 |
p. 973-977
|
artikel
|
| 17 |
Targeted Therapies for Leigh Syndrome: Systematic Review and Steps Towards a ‘Treatabolome’
|
Tiet, May Yung
|
|
|
8 |
6 |
p. 885-897
|
artikel
|
| 18 |
The Minimal Clinical Important Difference (MCID) in Annual Rate of Change of Timed Function Tests in Boys with DMD
|
Duong, Tina
|
|
|
8 |
6 |
p. 939-948
|
artikel
|
| 19 |
The Rare Knowledge Mining Methodological Framework for the Development of Practice Guidelines and Knowledge Translation Tools for Rare Diseases
|
Gagnon, C.
|
|
|
8 |
6 |
p. 1017-1029
|
artikel
|
| 20 |
What Happened with Muscle Force, Dynamic Stability And Falls? A 10-Year Longitudinal Follow-Up in Adults with Myotonic Dystrophy Type 1
|
Hammarén, Elisabet
|
|
|
8 |
6 |
p. 1007-1016
|
artikel
|
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