| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abnormal distribution of heterogeneous nuclear ribonucleoproteins in sporadic inclusion body myositis
|
Pinkus, Jack L.
|
|
2014
|
24 |
7 |
p. 611-616
6 p.
|
artikel
|
| 2 |
A novel mutation in PNPLA2 causes neutral lipid storage disease with myopathy and triglyceride deposit cardiomyovasculopathy: A case report and literature review
|
Kaneko, Kimihiko
|
|
2014
|
24 |
7 |
p. 634-641
8 p.
|
artikel
|
| 3 |
A novel quantitative morphometry approach to assess regeneration in dystrophic skeletal muscle
|
Buttgereit, Andreas
|
|
2014
|
24 |
7 |
p. 596-603
8 p.
|
artikel
|
| 4 |
Assessment of intramuscular lipid and metabolites of the lower leg using magnetic resonance spectroscopy in boys with Duchenne muscular dystrophy
|
Lott, Donovan J.
|
|
2014
|
24 |
7 |
p. 574-582
9 p.
|
artikel
|
| 5 |
Atrio-ventricular block requiring pacemaker in patients with late onset Pompe disease
|
Sacconi, Sabrina
|
|
2014
|
24 |
7 |
p. 648-650
3 p.
|
artikel
|
| 6 |
Deep sequencing detects very-low-grade somatic mosaicism in the unaffected mother of siblings with nemaline myopathy
|
Miyatake, Satoko
|
|
2014
|
24 |
7 |
p. 642-647
6 p.
|
artikel
|
| 7 |
Editorial Board
|
|
|
2014
|
24 |
7 |
p. IFC-
1 p.
|
artikel
|
| 8 |
Four-year longitudinal study of clinical and functional endpoints in sporadic inclusion body myositis: Implications for therapeutic trials
|
Hogrel, Jean-Yves
|
|
2014
|
24 |
7 |
p. 604-610
7 p.
|
artikel
|
| 9 |
Long-term administration of the TNF blocking drug Remicade (cV1q) to mdx mice reduces skeletal and cardiac muscle fibrosis, but negatively impacts cardiac function
|
Ermolova, N.V.
|
|
2014
|
24 |
7 |
p. 583-595
13 p.
|
artikel
|
| 10 |
Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies
|
Kayman-Kurekci, Gulsum
|
|
2014
|
24 |
7 |
p. 624-633
10 p.
|
artikel
|
| 11 |
Novel point mutations in survival motor neuron 1 gene expand the spectrum of phenotypes observed in spinal muscular atrophy patients
|
Jędrzejowska, Maria
|
|
2014
|
24 |
7 |
p. 617-623
7 p.
|
artikel
|
| 12 |
Proteomics profiling of urine reveals specific titin fragments as biomarkers of Duchenne muscular dystrophy
|
Rouillon, Jeremy
|
|
2014
|
24 |
7 |
p. 563-573
11 p.
|
artikel
|
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