| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Asymmetrical anterior thigh muscle atrophy as an atypical presentation of RYR1-core myopathy
|
Primiano, Guido
|
|
|
31 |
8 |
p. 798-799
|
artikel
|
| 2 |
Cerebral involvement and related aspects in myotonic dystrophy type 2
|
Peric, Stojan
|
|
|
31 |
8 |
p. 681-694
|
artikel
|
| 3 |
Characteristics of Guillain-Barré syndrome in a Lebanese tertiary care center
|
Ismail, Helen
|
|
|
31 |
8 |
p. 765-768
|
artikel
|
| 4 |
Characteristics of VCP mutation-associated cardiomyopathy
|
Wang, Stephani C.
|
|
|
31 |
8 |
p. 701-705
|
artikel
|
| 5 |
Editorial Board
|
|
|
|
31 |
8 |
p. IFC
|
artikel
|
| 6 |
Fatigue, physical activity and associated factors in 779 patients with myasthenia gravis
|
Andersen, Linda Kahr
|
|
|
31 |
8 |
p. 716-725
|
artikel
|
| 7 |
Home-based exercise in autoimmune myasthenia gravis: A randomized controlled trial
|
Birnbaum, S
|
|
|
31 |
8 |
p. 726-735
|
artikel
|
| 8 |
Intrafamilial phenotypic heterogeneity related to a new DMD splice site variant
|
Coimbra Neto, Antônio Rodrigues
|
|
|
31 |
8 |
p. 788-797
|
artikel
|
| 9 |
Late onset Sandhoff disease presenting with lower motor neuron disease and stuttering
|
Alonso-Pérez, Jorge
|
|
|
31 |
8 |
p. 769-772
|
artikel
|
| 10 |
Leukoencephalopathy and conduction blocks in PLEKHG5-associated intermediate CMT disease
|
Villar-Quiles, Rocio-Nur
|
|
|
31 |
8 |
p. 756-764
|
artikel
|
| 11 |
Musculoskeletal magnetic resonance imaging in the DE50-MD dog model of Duchenne muscular dystrophy
|
Hornby, Natasha L.
|
|
|
31 |
8 |
p. 736-751
|
artikel
|
| 12 |
New subtype of PCH1C caused by novel EXOSC8 variants in a 16-year-old Spanish patient
|
Rodríguez-García, María Elena
|
|
|
31 |
8 |
p. 773-782
|
artikel
|
| 13 |
Novel compound heterozygous TTN variants as a cause of severe neonatal congenital contracture syndrome without cardiac involvement diagnosed with rapid trio exome sequencing
|
McDermott, Helen
|
|
|
31 |
8 |
p. 783-787
|
artikel
|
| 14 |
Reliability and validity of the FSHD-composite outcome measure in childhood facioscapulohumeral dystrophy
|
de Valle, K.
|
|
|
31 |
8 |
p. 706-715
|
artikel
|
| 15 |
The phenotypic and genotypic features of a Scottish cohort with McArdle disease
|
Gandhi, Sacha E.
|
|
|
31 |
8 |
p. 695-700
|
artikel
|
| 16 |
Three cases of adult-onset Brown-Vialetto-Van Laere syndrome: Novel variants in SLC52A3 gene and MRI abnormalities
|
Carey, Guillaume
|
|
|
31 |
8 |
p. 752-755
|
artikel
|
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