| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A cross-sectional study of hand function in inclusion body myositis: Implications for functional rating scale
|
Lin, Ava Yun
|
|
|
30 |
3 |
p. 200-206
|
artikel
|
| 2 |
A hospital based epidemiological study of genetically determined muscle disease in south western Norway
|
Husebye, Sylvia Adele
|
|
|
30 |
3 |
p. 181-185
|
artikel
|
| 3 |
A novel heterozygous mutation in the C-terminal region of HSPB8 leads to limb-girdle rimmed vacuolar myopathy
|
Nicolau, Stefan
|
|
|
30 |
3 |
p. 236-240
|
artikel
|
| 4 |
A rare case of adult onset LPIN1 associated rhabdomyolysis
|
Minton, Thomas
|
|
|
30 |
3 |
p. 241-245
|
artikel
|
| 5 |
Association of fingerprint bodies with rods in a case with mutations in the LMOD3 gene
|
Marguet, Florent
|
|
|
30 |
3 |
p. 207-212
|
artikel
|
| 6 |
Clinical and electrophysiological evaluation of myasthenic features in an alpha-dystroglycanopathy cohort (FKRP-predominant)
|
Gonzalez-Perez, Paloma
|
|
|
30 |
3 |
p. 213-218
|
artikel
|
| 7 |
Clinical and histological features of immune-mediated necrotising myopathy: A multi-centre South Australian cohort study
|
Day, Jessica
|
|
|
30 |
3 |
p. 186-199
|
artikel
|
| 8 |
Editorial Board
|
|
|
|
30 |
3 |
p. IFC
|
artikel
|
| 9 |
Identification of novel SMN1 subtle mutations using an allelic-specific RT-PCR
|
Xu, Yan
|
|
|
30 |
3 |
p. 219-226
|
artikel
|
| 10 |
Inherited motor-sensory neuropathy with upper limb predominance associated with the tropomyosin-receptor kinase fused gene
|
Fabrizi, Gian Maria
|
|
|
30 |
3 |
p. 227-231
|
artikel
|
| 11 |
Myasthenia gravis after etanercept and ustekinumab treatment for psoriatic arthritis: A case report
|
Nicocia, Giulia
|
|
|
30 |
3 |
p. 246-249
|
artikel
|
| 12 |
242nd ENMC International Workshop: Diagnosis and management of juvenile myasthenia gravis Hoofddorp, the Netherlands, 1–3 March 2019
|
Munot, Pinki
|
|
|
30 |
3 |
p. 254-264
|
artikel
|
| 13 |
Phenotypic convergence in Charcot-Marie-Tooth 2Y with novel VCP mutation
|
Gite, Jasmine
|
|
|
30 |
3 |
p. 232-235
|
artikel
|
| 14 |
Response to “Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype”
|
Rossi, Salvatore
|
|
|
30 |
3 |
p. 265-266
|
artikel
|
| 15 |
The mysterious death of Georges Cuvier (1832): An early case of severe Guillain–Barré syndrome?
|
Mathis, Stéphane
|
|
|
30 |
3 |
p. 250-253
|
artikel
|
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