| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Comparing Deflazacort and Prednisone in Duchenne Muscular Dystrophy
|
Biggar, W. Douglas
|
|
|
9 |
4 |
p. 463-476
|
artikel
|
| 2 |
Genetic Appraisal of Hereditary Muscle Disorders In A Cohort From Mumbai, India
|
Khadilkar, Satish Vasant
|
|
|
9 |
4 |
p. 571-580
|
artikel
|
| 3 |
GFPT1-Associated Congenital Myasthenic Syndrome Mimicking a Glycogen Storage Disease – Diagnostic Pitfalls in Myopathology Solved by Next-Generation-Sequencing
|
Mensch, Alexander
|
|
|
9 |
4 |
p. 533-541
|
artikel
|
| 4 |
INCEPTUS Natural History, Run-in Study for Gene Replacement Clinical Trial in X-Linked Myotubular Myopathy
|
Dowling, James J.
|
|
|
9 |
4 |
p. 503-516
|
artikel
|
| 5 |
Long-Term Functional Efficacy and Safety of Viltolarsen in Patients with Duchenne Muscular Dystrophy
|
Clemens, Paula R.
|
|
|
9 |
4 |
p. 493-501
|
artikel
|
| 6 |
Progression to Loss of Ambulation Among Patients with Autosomal Recessive Limb-girdle Muscular Dystrophy: A Systematic Review
|
Audhya, Ivana F.
|
|
|
9 |
4 |
p. 477-492
|
artikel
|
| 7 |
Slow Channel Syndrome Revisited: 40 Years Clinical Follow-Up and Genetic Characterization of Two Cases
|
Boon, Helena T.M.
|
|
|
9 |
4 |
p. 525-532
|
artikel
|
| 8 |
The Black Box of Technological Outcome Measures: An Example in Duchenne Muscular Dystrophy
|
Naarding, Karin J.
|
|
|
9 |
4 |
p. 555-569
|
artikel
|
| 9 |
The neurocognitive profile of adults with Becker muscular dystrophy in the Netherlands
|
Koeks, Zaıda
|
|
|
9 |
4 |
p. 543-553
|
artikel
|
| 10 |
Understanding the Perseverance of the Muscular Dystrophy Community One-Year into the COVID-19 Pandemic
|
Lewis, Leann
|
|
|
9 |
4 |
p. 517-523
|
artikel
|
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