| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A rare case of monozygotic triplets with Duchenne muscular dystrophy
|
Wang, Liang
|
|
|
31 |
5 |
p. 456-461
|
artikel
|
| 2 |
Clinical and genetic characteristics of Chinese patients with reducing body myopathy
|
Chen, Lei
|
|
|
31 |
5 |
p. 442-449
|
artikel
|
| 3 |
Disease-modifying effects of edasalonexent, an NF-κB inhibitor, in young boys with Duchenne muscular dystrophy: Results of the MoveDMD phase 2 and open label extension trial
|
Finkel, Richard S.
|
|
|
31 |
5 |
p. 385-396
|
artikel
|
| 4 |
Editorial Board
|
|
|
|
31 |
5 |
p. IFC
|
artikel
|
| 5 |
Filling the gaps in knowledge translation: Physical therapy recommendations for individuals with spinal muscular atrophy compared to standard of care guidelines
|
Trenkle, Jessica
|
|
|
31 |
5 |
p. 397-408
|
artikel
|
| 6 |
Importance of immunohistochemical evaluation of developmentally regulated myosin heavy chains in human muscle biopsies
|
Sewry, C.A.
|
|
|
31 |
5 |
p. 371-384
|
artikel
|
| 7 |
Late-onset camptocormia caused by a heterozygous in-frame CAPN3 deletion
|
Spinazzi, Marco
|
|
|
31 |
5 |
p. 450-455
|
artikel
|
| 8 |
Late onset Pompe Disease in India – Beyond the Caucasian phenotype
|
Puri, Ratna Dua
|
|
|
31 |
5 |
p. 431-441
|
artikel
|
| 9 |
251st ENMC international workshop: Polyglucosan storage myopathies 13–15 December 2019, Hoofddorp, the Netherlands
|
Laforêt, Pascal
|
|
|
31 |
5 |
p. 466-477
|
artikel
|
| 10 |
The Spinal Muscular Atrophy Health Index: Italian validation of a disease-specific outcome measure
|
Sansone, Valeria A.
|
|
|
31 |
5 |
p. 409-418
|
artikel
|
| 11 |
Third case of Duchenne muscular dystrophy and West syndrome: Expanding the spectrum of the DMD neuropsychiatric phenotype
|
Peña-Padilla, Christian
|
|
|
31 |
5 |
p. 462-465
|
artikel
|
| 12 |
Understanding European patient expectations towards current therapeutic development in spinal muscular atrophy
|
Gusset, Nicole
|
|
|
31 |
5 |
p. 419-430
|
artikel
|
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