| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Andersen-Tawil Syndrome with Early Onset Myopathy: 2 Cases
|
Oz Tuncer, Gokcen
|
|
2017
|
4 |
1 |
p. 93-95
|
artikel
|
| 2 |
Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy
|
Fayssoil, Abdallah
|
|
2017
|
4 |
1 |
p. 17-23
|
artikel
|
| 3 |
Cysteine Supplementation May be Beneficial in a Subgroup of Mitochondrial Translation Deficiencies
|
Bartsakoulia, Marina
|
|
2017
|
4 |
1 |
p. 97
|
artikel
|
| 4 |
Histopathologic and Biochemical Evidence for Mitochondrial Disease Among 279 Patients with Severe Statin Myopathy
|
Hou, Tieying
|
|
2017
|
4 |
1 |
p. 77-87
|
artikel
|
| 5 |
Measuring Habitual Physical Activity in Neuromuscular Disorders: A Systematic Review
|
Jimenez-Moreno, Aura Cecilia
|
|
2017
|
4 |
1 |
p. 25-52
|
artikel
|
| 6 |
Myofibrillar Myopathies: New Perspectives from Animal Models to Potential Therapeutic Approaches
|
Batonnet-Pichon, Sabrina
|
|
2017
|
4 |
1 |
p. 1-15
|
artikel
|
| 7 |
Neuromyelitis Optica in a Patient from Family with both Myotonic Dystrophy Type 1 and 2
|
Rakocevic-Stojanovic, V.
|
|
2017
|
4 |
1 |
p. 89-92
|
artikel
|
| 8 |
Proton Magnetic Resonance Spectroscopy Indicates Preserved Cerebral Biochemical Composition in Duchenne Muscular Dystrophy Patients
|
Doorenweerd, Nathalie
|
|
2017
|
4 |
1 |
p. 53-58
|
artikel
|
| 9 |
RYR1-Related Myopathies: Clinical, Histopathologic and Genetic Heterogeneity Among 17 Patients from a Portuguese Tertiary Centre
|
Samões, Raquel
|
|
2017
|
4 |
1 |
p. 67-76
|
artikel
|
| 10 |
SMN Blood Levels in a Porcine Model of Spinal Muscular Atrophy
|
Iyer, Chitra
|
|
2017
|
4 |
1 |
p. 59-66
|
artikel
|
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