| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel de novo ACTA1 variant in a patient with nemaline myopathy and mitochondrial Complex I deficiency
|
Pula, Shpresa
|
|
|
30 |
2 |
p. 159-164
|
artikel
|
| 2 |
Clinical and genetic characterization of limb girdle muscular dystrophy R7 telethonin-related patients from three unrelated Chinese families
|
Chen, Haizhu
|
|
|
30 |
2 |
p. 137-143
|
artikel
|
| 3 |
Cylindrical spirals in two families: Clinical and genetic investigations
|
Beecroft, Sarah J
|
|
|
30 |
2 |
p. 151-158
|
artikel
|
| 4 |
Editorial Board
|
|
|
|
30 |
2 |
p. IFC
|
artikel
|
| 5 |
Emerging therapies for autoimmune myasthenia gravis: Towards treatment without corticosteroids
|
Tannemaat, Martijn R.
|
|
|
30 |
2 |
p. 111-119
|
artikel
|
| 6 |
FHL1-related myopathy may not be classified by reducing bodies in muscle biopsy
|
Chen, Ting
|
|
|
30 |
2 |
p. 165-172
|
artikel
|
| 7 |
Improving specialised care for neuromuscular patients reduces the frequency of preventable emergency hospital admissions
|
Scalco, Renata S.
|
|
|
30 |
2 |
p. 173-179
|
artikel
|
| 8 |
Management of the dentoalveolar effects of tongue hypertrophy in patients with Duchenne muscular dystrophy: A pilot study
|
Antonarakis, Gregory S.
|
|
|
30 |
2 |
p. 105-110
|
artikel
|
| 9 |
Myopathies presenting with head drop: Clinical spectrum and treatment outcomes
|
Alhammad, Reem M.
|
|
|
30 |
2 |
p. 128-136
|
artikel
|
| 10 |
Paediatric myasthenia gravis: Prognostic factors for drug free remission
|
Vecchio, Domizia
|
|
|
30 |
2 |
p. 120-127
|
artikel
|
| 11 |
Spectral domain optical coherence tomography findings in myotonic dystrophy
|
Abed, Edoardo
|
|
|
30 |
2 |
p. 144-150
|
artikel
|
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