| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Multidisciplinary Perspective Addressing the Diagnostic Challenges of Late-Onset Pompe Disease in the Arabian Peninsula Region Developed From an Expert Group Meeting
|
Al Shehri, Ali
|
|
|
9 |
5 |
p. 661-673
|
artikel
|
| 2 |
Congenital or Early Developing Neuromuscular Diseases Affecting Feeding, Swallowing and Speech – A Review of the Literature from January 1998 to August 2021
|
Sjögreen, Lotta
|
|
|
9 |
5 |
p. 581-596
|
artikel
|
| 3 |
Diagnostic Yield of Chilaiditi’s Sign in Advanced-Phase Late-Onset Pompe Disease
|
Takahashi, Junichiro
|
|
|
9 |
5 |
p. 619-627
|
artikel
|
| 4 |
Expanding the MYOD1 Phenotype: A Case Report of a Patient Diagnosed Whilst Pregnant
|
Ashton, Catherine
|
|
|
9 |
5 |
p. 615-618
|
artikel
|
| 5 |
Impact of a 12-week Strength Training Program on Fatigue, Daytime Sleepiness, and Apathy in Men with Myotonic Dystrophy Type 1
|
Gallais, Benjamin
|
|
|
9 |
5 |
p. 629-639
|
artikel
|
| 6 |
Muscle MRI as a Diagnostic Challenge in Emery-Dreifuss Muscular Dystrophy
|
Pinto, Maria João
|
|
|
9 |
5 |
p. 649-654
|
artikel
|
| 7 |
Newborn Screening for SMA – Can a Wait-and-See Strategy be Responsibly Justified in Patients With Four SMN2 Copies?
|
Blaschek, Astrid
|
|
|
9 |
5 |
p. 597-605
|
artikel
|
| 8 |
Orthopedic Interventions for Foot Deformities in Non-Ambulant People with Duchenne Muscular Dystrophy: A Retrospective Study on Indications, Post-Operative and Long-Term Outcomes
|
Houwen-van Opstal, Saskia L.S.
|
|
|
9 |
5 |
p. 641-648
|
artikel
|
| 9 |
Real-world Adherence to Nusinersen in Adults with Spinal Muscular Atrophy in the US: A Multi-site Chart Review Study
|
Elman, Lauren
|
|
|
9 |
5 |
p. 655-660
|
artikel
|
| 10 |
Slowly Progressive Limb-Girdle Weakness and HyperCKemia – Limb Girdle Muscular Dystrophy or Anti-3-Hydroxy-3-Methylglutaryl-CoA-Reductase-Myopathy?
|
Hiebeler, Miriam
|
|
|
9 |
5 |
p. 607-614
|
artikel
|
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