nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A c.1775C > T Point Mutation of Sodium Channel Alfa Subunit Gene (SCN4A) in a Three-Generation Sardinian Family with Sodium Channel Myotonia
|
Campanale, Carmen |
|
|
11 |
3 |
p. 725-734 |
artikel |
2 |
Detection of Autoantibodies Against the Acetylcholine Receptor, Evaluation of Commercially Available Methodologies: Fixed Cell-Based Assay, Radioimmunoprecipitation Assay and Enzyme-Linked Immunosorbent Assay1
|
Diogenes, Larissa |
|
|
11 |
3 |
p. 613-623 |
artikel |
3 |
Disease Trajectories in the Revised Hammersmith Scale in a Cohort of Untreated Patients with Spinal Muscular Atrophy types 2 and 3
|
Wolfe, Amy |
|
|
11 |
3 |
p. 665-677 |
artikel |
4 |
Improving Diagnostic Precision: Phenotype-Driven Analysis Uncovers a Maternal Mosaicism in an Individual with RYR1-Congenital Myopathy
|
Estévez-Arias, Berta |
|
|
11 |
3 |
p. 647-653 |
artikel |
5 |
Increase in Full-Length Dystrophin by Exon Skipping in Duchenne Muscular Dystrophy Patients with Single Exon Duplications: An Open-label Study
|
Nicolau, Stefan |
|
|
11 |
3 |
p. 679-685 |
artikel |
6 |
Management of Select Adverse Events Following Delandistrogene Moxeparvovec Gene Therapy for Patients With Duchenne Muscular Dystrophy
|
Zaidman, Craig M. |
|
|
11 |
3 |
p. 687-699 |
artikel |
7 |
Natural History of Mandibular Function in Spinal Muscular Atrophy Types 2 and 3
|
van Bruggen, H. Willemijn |
|
|
11 |
3 |
p. 655-664 |
artikel |
8 |
Novel Genetic and Biochemical Insights into the Spectrum of NEFL-Associated Phenotypes
|
Della Marina, Adela |
|
|
11 |
3 |
p. 625-645 |
artikel |
9 |
Patient-Reported Outcome Measures in Neuromuscular Diseases: A Scoping Review
|
Voet, Nicoline |
|
|
11 |
3 |
p. 567-577 |
artikel |
10 |
Predictors of Loss of Ambulation in Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis
|
Landfeldt, E. |
|
|
11 |
3 |
p. 579-612 |
artikel |
11 |
Stride Velocity 95th Centile Detects Decline in Ambulatory Function Over Shorter Intervals than the 6-Minute Walk Test or North Star Ambulatory Assessment in Duchenne Muscular Dystrophy
|
Rabbia, Michael |
|
|
11 |
3 |
p. 701-714 |
artikel |
12 |
The Association Between Physical Activity/Heart Rate Variability Data Obtained Using a Wearable Device and Timed Motor Functional Tests in Patients with Duchenne Muscular Dystrophy: A Pilot Study
|
Nakamura, Akinori |
|
|
11 |
3 |
p. 715-724 |
artikel |
13 |
Treatment Approaches for Altered Facial Expression: A Systematic Review in Facioscapulohumeral Muscular Dystrophy and Other Neurological Diseases
|
Rasing, Nathaniël B. |
|
|
11 |
3 |
p. 535-565 |
artikel |