nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcome
|
Wahbi, Karim |
|
2016 |
26 |
3 |
p. 227-233 7 p. |
artikel |
2 |
Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers
|
Vainzof, Mariz |
|
2016 |
26 |
3 |
p. 197-200 4 p. |
artikel |
3 |
De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion
|
Pajusalu, Sander |
|
2016 |
26 |
3 |
p. 236-239 4 p. |
artikel |
4 |
Editorial Board
|
|
|
2016 |
26 |
3 |
p. CO2- 1 p. |
artikel |
5 |
Health-related quality of life and functional changes in DMD: A 12-month longitudinal cohort study
|
Messina, Sonia |
|
2016 |
26 |
3 |
p. 189-196 8 p. |
artikel |
6 |
How robust is ACTIVLIM for the follow-up of activity limitations in patients with neuromuscular diseases?
|
Batcho, Charles Sèbiyo |
|
2016 |
26 |
3 |
p. 211-220 10 p. |
artikel |
7 |
Muscle from a 20-week-old myotubular myopathy fetus is not myotubular
|
Hamanaka, Kohei |
|
2016 |
26 |
3 |
p. 234-235 2 p. |
artikel |
8 |
Neuromuscular conditions associated with malignant hyperthermia in paediatric patients: A 25-year retrospective study
|
Bamaga, Ahmed K. |
|
2016 |
26 |
3 |
p. 201-206 6 p. |
artikel |
9 |
Recurrent episodes of myoglobinuria, mental retardation and seizures but no hemolysis in two brothers with phosphoglycerate kinase deficiency
|
Coppens, Sandra |
|
2016 |
26 |
3 |
p. 207-210 4 p. |
artikel |
10 |
The Dutch patients' perspective on oculopharyngeal muscular dystrophy: A questionnaire study on fatigue, pain and impairments
|
van der Sluijs, Barbara M. |
|
2016 |
26 |
3 |
p. 221-226 6 p. |
artikel |
11 |
212th ENMC International Workshop:
|
Saunier, M. |
|
2016 |
26 |
3 |
p. 252-259 8 p. |
artikel |
12 |
Thrombospondin-1 levels correlate with macrophage activity and disease progression in dysferlin deficient mice
|
Urao, Norifumi |
|
2016 |
26 |
3 |
p. 240-251 12 p. |
artikel |