| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acute weakness and elevated creatine kinase levels associated with coxsackievirus infection in LAMA2-related muscular dystrophy
|
Wong, Wui-Kwan
|
|
|
45 |
C |
p.
|
artikel
|
| 2 |
Concurrent nodular lymphocytic myositis and myasthenia gravis. A case report
|
D'Ambrosio, Eleonora S
|
|
|
45 |
C |
p.
|
artikel
|
| 3 |
Early diagnosis of Duchenne muscular dystrophy - A Treat-NMD international workshop
|
Lorentzos, M.
|
|
|
45 |
C |
p.
|
artikel
|
| 4 |
Editorial Board
|
|
|
|
45 |
C |
p.
|
artikel
|
| 5 |
ENMC Themed Workshop announcement
|
|
|
|
45 |
C |
p.
|
artikel
|
| 6 |
Genotype and corticosteroid treatment are distinctively associated with gray matter characteristics in patients with Duchenne muscular dystrophy
|
Geuens, Sam
|
|
|
45 |
C |
p.
|
artikel
|
| 7 |
Mitochondrial disorders are associated with morphological neuromuscular junction defects
|
Lessard, Lola E. R.
|
|
|
45 |
C |
p.
|
artikel
|
| 8 |
Paediatric neuromuscular diseases in Africa: access to care
|
Raga, Sharika
|
|
|
45 |
C |
p.
|
artikel
|
| 9 |
273rd ENMC International workshop: Clinico-Sero-morphological classification of the Antisynthetase syndrome. Amsterdam, The Netherlands, 27-29 October 2023
|
Stenzel, Werner
|
|
|
45 |
C |
p.
|
artikel
|
| 10 |
Two novel deep intronic variants cause Duchenne muscular dystrophy by splice-altering mechanism
|
Zhao, Lei
|
|
|
45 |
C |
p.
|
artikel
|
| 11 |
Very-late-onset multiple Acyl-coenzyme a dehydrogenase deficiency with elevated GDF-15 and Aldolase: a case report
|
Gaini, Rahul
|
|
|
45 |
C |
p.
|
artikel
|
| 12 |
Vienna WMS 2025
|
|
|
|
45 |
C |
p.
|
artikel
|
| 13 |
WMS General Information
|
|
|
|
45 |
C |
p.
|
artikel
|
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