| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Circulating Biomarkers for Duchenne Muscular Dystrophy
|
Aartsma-Rus, Annemieke
|
|
2015
|
2 |
s2 |
p. S49-S58
|
artikel
|
| 2 |
Congenital Myasthenic Syndromes with Predominant Limb Girdle Weakness
|
Evangelista, Teresinha
|
|
2015
|
2 |
s2 |
p. S21-S29
|
artikel
|
| 3 |
Editorial
|
Lochmüller, Hanns
|
|
2015
|
2 |
s2 |
p. S1
|
artikel
|
| 4 |
Exosomal Protein Deficiencies: How Abnormal RNA Metabolism Results in Childhood-Onset Neurological Diseases
|
Müller, Juliane S.
|
|
2015
|
2 |
s2 |
p. S31-S37
|
artikel
|
| 5 |
GNE Myopathy: Two Clusters with History and Several Founder Mutations
|
Argov, Zohar
|
|
2015
|
2 |
s2 |
p. S73-S76
|
artikel
|
| 6 |
John Walton – Inspiration and Founder of Muscular Dystrophy UK
|
Meadowcroft, Robert
|
|
2015
|
2 |
s2 |
p. S5-S6
|
artikel
|
| 7 |
John Walton (Lord Walton of Detchant)
|
Walton, John
|
|
2015
|
2 |
s2 |
p. S3-S4
|
artikel
|
| 8 |
Looking Forward to New Therapies: A Personal Perspective on the Translational Landscape for Muscular Dystrophies
|
Bushby, Kate
|
|
2015
|
2 |
s2 |
p. S83-S87
|
artikel
|
| 9 |
Lord Walton of Detchant: There and Back Again
|
Chinnery, Patrick F.
|
|
2015
|
2 |
s2 |
p. S89-S94
|
artikel
|
| 10 |
Myotonic Dystrophy Type 2: An Update on Clinical Aspects, Genetic and Pathomolecular Mechanism
|
Meola, Giovanni
|
|
2015
|
2 |
s2 |
p. S59-S71
|
artikel
|
| 11 |
The Classification, Natural History and Treatment of the Limb Girdle Muscular Dystrophies
|
Murphy, Alexander Peter
|
|
2015
|
2 |
s2 |
p. S7-S19
|
artikel
|
| 12 |
The John Walton Muscular Dystrophy Research Centre in the University of Newcastle and the BMAA Theory of Motor Neuron Disease
|
Bradley, Walter G.
|
|
2015
|
2 |
s2 |
p. S77-S81
|
artikel
|
| 13 |
Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP):A Single-Center Experience in Sicily, an Italian Endemic Area
|
Mazzeo, Anna
|
|
2015
|
2 |
s2 |
p. S39-S48
|
artikel
|
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