| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A cross-sectional analysis of clinical evaluation in 35 individuals with mutations of the valosin-containing protein gene
|
Plewa, Jake
|
|
2018
|
28 |
9 |
p. 778-786
|
artikel
|
| 2 |
Advances in the diagnosis and management of cardiomyopathy in Duchenne muscular dystrophy
|
Hor, Kan N.
|
|
2018
|
28 |
9 |
p. 711-716
|
artikel
|
| 3 |
An integrated modelling methodology for estimating the prevalence of centronuclear myopathy
|
Vandersmissen, I.
|
|
2018
|
28 |
9 |
p. 766-777
|
artikel
|
| 4 |
A recurrent de novo DYNC1H1 tail domain mutation causes spinal muscular atrophy with lower extremity predominance, learning difficulties and mild brain abnormality
|
Chan, Sophelia Hoi Shan
|
|
2018
|
28 |
9 |
p. 750-756
|
artikel
|
| 5 |
BAG3 myopathy is not always associated with cardiomyopathy
|
Andersen, Annarita Ghosh
|
|
2018
|
28 |
9 |
p. 798-801
|
artikel
|
| 6 |
Clinical spectrum, treatment and outcome of children with suspected diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy
|
Silwal, A.
|
|
2018
|
28 |
9 |
p. 757-765
|
artikel
|
| 7 |
ECEL1 gene related contractural syndrome: Long-term follow-up and update on clinical and pathological aspects
|
Ullmann, Urielle
|
|
2018
|
28 |
9 |
p. 741-749
|
artikel
|
| 8 |
Editorial Board
|
|
|
2018
|
28 |
9 |
p. IFC
|
artikel
|
| 9 |
Imaging the heart to detect cardiomyopathy in Duchenne muscular dystrophy: A review
|
Power, Lisa C.
|
|
2018
|
28 |
9 |
p. 717-730
|
artikel
|
| 10 |
Juvenile dermatomyositis forty years on: Case report
|
Rego de Figueiredo, Inês
|
|
2018
|
28 |
9 |
p. 791-797
|
artikel
|
| 11 |
Post-mortem detection of FLAD1 mutations in 2 Turkish siblings with hypotonia in early infancy
|
Yıldız, Yılmaz
|
|
2018
|
28 |
9 |
p. 787-790
|
artikel
|
| 12 |
Respiratory insight to congenital muscular dystrophies and congenital myopathies and its relation to clinical trial
|
Fauroux, Brigitte
|
|
2018
|
28 |
9 |
p. 731-740
|
artikel
|
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