| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An overview of the Cure SMA membership database: Highlights of key demographic and clinical characteristics of SMA members
|
Belter, Lisa
|
|
2018
|
5 |
2 |
p. 167-176
|
artikel
|
| 2 |
A Qualitative Approach to Health Related Quality-of-Life in Congenital Muscular Dystrophy
|
Cornwall, Kylie M.
|
|
2018
|
5 |
2 |
p. 251-255
|
artikel
|
| 3 |
Beta-2 Adrenergic Receptor Agonists Enhance AChR Clustering in C2C12 Myotubes: Implications for Therapy of Myasthenic Disorders
|
Clausen, Lisa
|
|
2018
|
5 |
2 |
p. 231-240
|
artikel
|
| 4 |
Characteristics of Japanese Patients with Becker Muscular Dystrophy and Intermediate Muscular Dystrophy in a Japanese National Registry of Muscular Dystrophy (Remudy): Heterogeneity and Clinical Variation
|
Mori-Yoshimura, Madoka
|
|
2018
|
5 |
2 |
p. 193-203
|
artikel
|
| 5 |
Current Classification and Management of Inflammatory Myopathies
|
Schmidt, Jens
|
|
2018
|
5 |
2 |
p. 109-129
|
artikel
|
| 6 |
Determination of qPCR Reference Genes Suitable for Normalizing Gene Expression in a Canine Model of Duchenne Muscular Dystrophy
|
Hildyard, John C.W.
|
|
2018
|
5 |
2 |
p. 177-191
|
artikel
|
| 7 |
Efficacy of Rituximab in Refractory Generalized anti-AChR Myasthenia Gravis
|
Landon-Cardinal, Océane
|
|
2018
|
5 |
2 |
p. 241-249
|
artikel
|
| 8 |
Evaluation of Children with SMA Type 1 Under Treatment with Nusinersen within the Expanded Access Program in Germany
|
Pechmann, Astrid
|
|
2018
|
5 |
2 |
p. 135-143
|
artikel
|
| 9 |
Evaluator Training and Reliability for SMA Global Nusinersen Trials1
|
Glanzman, Allan M.
|
|
2018
|
5 |
2 |
p. 159-166
|
artikel
|
| 10 |
Novel SPEG Mutations in Congenital Myopathy without Centralized Nuclei
|
Lornage, Xavière
|
|
2018
|
5 |
2 |
p. 257-260
|
artikel
|
| 11 |
Participation and the Role of Neuropsychological Functioning in Myotonic Dystrophy Type 1
|
Van Heugten, Caroline
|
|
2018
|
5 |
2 |
p. 205-214
|
artikel
|
| 12 |
Position Statement: Sharing of Clinical Research Data in Spinal Muscular Atrophy to Accelerate Research and Improve Outcomes for Patients
|
Lochmüller, Hanns
|
|
2018
|
5 |
2 |
p. 131-133
|
artikel
|
| 13 |
Problems in Comparing Jitter Values Obtained with Voluntary Activation and Electrical Stimulation
|
Stålberg, Erik
|
|
2018
|
5 |
2 |
p. 225-230
|
artikel
|
| 14 |
Relationships between Lower Limb Muscle Strength Impairments and Physical Limitations in DM1
|
Petitclerc, Émilie
|
|
2018
|
5 |
2 |
p. 215-224
|
artikel
|
| 15 |
Serum Acetylcholine Receptor Antibodies Before the Clinical Onset of Myasthenia Gravis
|
Strijbos, Ellen
|
|
2018
|
5 |
2 |
p. 261-264
|
artikel
|
| 16 |
Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening
|
Glascock, Jacqueline
|
|
2018
|
5 |
2 |
p. 145-158
|
artikel
|
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