| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A new homozygous missense variant in LMOD3 gene causing mild nemaline myopathy with prominent facial weakness
|
Segarra-Casas, Alba
|
|
|
33 |
4 |
p. 319-323
|
artikel
|
| 2 |
A new score combining compound muscle action potential (CMAP) amplitudes and motor score is predictive of motor outcome after AVXS-101 (Onasemnogene Abeparvovec) SMA therapy
|
Barrois, R.
|
|
|
33 |
4 |
p. 309-314
|
artikel
|
| 3 |
Clinical characteristics and prognosis of very late-onset myasthenia gravis in China
|
Tang, Yong-Lan
|
|
|
33 |
4 |
p. 358-366
|
artikel
|
| 4 |
Editorial Board
|
|
|
|
33 |
4 |
p. IFC
|
artikel
|
| 5 |
Epidemiology and treatment of myasthenia gravis: a retrospective study using a large insurance claims dataset in Germany
|
Mevius, Antje
|
|
|
33 |
4 |
p. 324-333
|
artikel
|
| 6 |
Expanding the muscle imaging spectrum in dysferlinopathy: description of an outlier population from the classical MRI pattern
|
Llansó, Laura
|
|
|
33 |
4 |
p. 349-357
|
artikel
|
| 7 |
Implementation of tailored exercise programs for MG patients in a gym setting: a pragmatic feasibility case study
|
Punga, Anna Rostedt
|
|
|
33 |
4 |
p. 334-338
|
artikel
|
| 8 |
NMNAT1 and hereditary spastic paraplegia (HSP): expanding the phenotypic spectrum of NMNAT1 variants
|
Sadr, Zahra
|
|
|
33 |
4 |
p. 295-301
|
artikel
|
| 9 |
Successful management of rhabdomyolysis with triheptanoin in a child with severe long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency
|
Kahraman, Ayca Burcu
|
|
|
33 |
4 |
p. 315-318
|
artikel
|
| 10 |
266th ENMC International Workshop: Remote delivery of clinical care and validation of remote clinical outcome assessments in neuromuscular disorders: A response to COVID-19 and proactive planning for the future. Hoofddorp, The Netherlands, 1–3 April 2022
|
Alfano, Lindsay N.
|
|
|
33 |
4 |
p. 339-348
|
artikel
|
| 11 |
Update in Neuromuscular Disorders
|
|
|
|
33 |
4 |
p. I
|
artikel
|
| 12 |
Urine titin as a novel biomarker for Duchenne muscular dystrophy
|
Ishii, Misawa Niki
|
|
|
33 |
4 |
p. 302-308
|
artikel
|
| 13 |
WMS 2022 Congress announcement
|
|
|
|
33 |
4 |
p. IV
|
artikel
|
| 14 |
WMS 2022 Flyer
|
|
|
|
33 |
4 |
p. III
|
artikel
|
| 15 |
WMS Information
|
|
|
|
33 |
4 |
p. II
|
artikel
|
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