| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patients
|
Waddell, Leigh B.
|
|
2011
|
21 |
11 |
p. 776-781
6 p.
|
artikel
|
| 2 |
Combination of steroids and ischial weight-bearing knee ankle foot orthoses in Duchenne’s muscular dystrophy prolongs ambulation past 20years of age – A case report
|
Pardo, Andrea C.
|
|
2011
|
21 |
11 |
p. 800-802
3 p.
|
artikel
|
| 3 |
Deficiency of the mitochondrial phosphate carrier presenting as myopathy and cardiomyopathy in a family with three affected children
|
Mayr, Johannes A.
|
|
2011
|
21 |
11 |
p. 803-808
6 p.
|
artikel
|
| 4 |
Editorial Board
|
|
|
2011
|
21 |
11 |
p. IFC-
1 p.
|
artikel
|
| 5 |
Hereditary peripheral neuropathies of childhood: An overview for clinicians
|
Wilmshurst, Jo M.
|
|
2011
|
21 |
11 |
p. 763-775
13 p.
|
artikel
|
| 6 |
Intragenic rearrangements in LARGE and POMGNT1 genes in severe dystroglycanopathies
|
Vuillaumier-Barrot, S.
|
|
2011
|
21 |
11 |
p. 782-790
9 p.
|
artikel
|
| 7 |
Scoliosis surgery in a patient with “de novo” myosin storage myopathy
|
Stalpers, Xenia
|
|
2011
|
21 |
11 |
p. 812-815
4 p.
|
artikel
|
| 8 |
Two cases of oculopharyngeal muscular dystrophy (OPMD) with the rare PABPN1 c.35G>C; p.Gly12Ala point mutation
|
Robinson, David O.
|
|
2011
|
21 |
11 |
p. 809-811
3 p.
|
artikel
|
| 9 |
Whole-body muscle MRI in 20 patients suffering from late onset Pompe disease: Involvement patterns
|
Carlier, Robert-Yves
|
|
2011
|
21 |
11 |
p. 791-799
9 p.
|
artikel
|
| 10 |
WMS 2012
|
|
|
2011
|
21 |
11 |
p. 816-
1 p.
|
artikel
|
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