| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Ambulatory capacity and disease progression as measured by the 6-minute-walk-distance in Duchenne muscular dystrophy subjects on daily corticosteroids
|
Goemans, Nathalie
|
|
2013
|
23 |
8 |
p. 618-623
6 p.
|
artikel
|
| 2 |
A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot–Marie–Tooth disease type 2L
|
Nakhro, Khriezhanuo
|
|
2013
|
23 |
8 |
p. 656-663
8 p.
|
artikel
|
| 3 |
Charcot-Marie-Tooth disease: Frequency of genetic subtypes in a German neuromuscular center population
|
Gess, Burkhard
|
|
2013
|
23 |
8 |
p. 647-651
5 p.
|
artikel
|
| 4 |
Compound heterozygous mutations of the TNXB gene cause primary myopathy
|
Pénisson-Besnier, Isabelle
|
|
2013
|
23 |
8 |
p. 664-669
6 p.
|
artikel
|
| 5 |
Creatine deficiency syndrome. A treatable myopathy due to arginine–glycine amidinotransferase (AGAT) deficiency
|
Nouioua, S.
|
|
2013
|
23 |
8 |
p. 670-674
5 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2013
|
23 |
8 |
p. IFC-
1 p.
|
artikel
|
| 7 |
Erratum to ‘Commentary from the Editor’ [Neuromuscul Disord 23 (2013) 1–3]
|
|
|
2013
|
23 |
8 |
p. 698-
1 p.
|
artikel
|
| 8 |
Lactate metabolism during exercise in patients with mitochondrial myopathy
|
Jeppesen, Tina D.
|
|
2013
|
23 |
8 |
p. 629-636
8 p.
|
artikel
|
| 9 |
Limb-girdle muscular dystrophy type 2I is not rare in Taiwan
|
Liang, Wen-Chen
|
|
2013
|
23 |
8 |
p. 675-681
7 p.
|
artikel
|
| 10 |
Muscle MRI reveals distinct abnormalities in genetically proven non-dystrophic myotonias
|
Morrow, Jasper M.
|
|
2013
|
23 |
8 |
p. 637-646
10 p.
|
artikel
|
| 11 |
Response
|
Dubowitz, Victor
|
|
2013
|
23 |
8 |
p. 697-
1 p.
|
artikel
|
| 12 |
Scoliosis in Duchenne muscular dystrophy (DMD)
|
Hsu, John D.
|
|
2013
|
23 |
8 |
p. 611-617
7 p.
|
artikel
|
| 13 |
Six minute walk test in type III spinal muscular atrophy: A 12month longitudinal study
|
Mazzone, E.
|
|
2013
|
23 |
8 |
p. 624-628
5 p.
|
artikel
|
| 14 |
Steroids in Duchenne muscular dystrophy
|
Ricotti, V.
|
|
2013
|
23 |
8 |
p. 696-697
2 p.
|
artikel
|
| 15 |
The first Japanese case of Charcot–Marie–Tooth disease type 4H with a novel FGD4 c.837-1G>A mutation
|
Arai, Hidee
|
|
2013
|
23 |
8 |
p. 652-655
4 p.
|
artikel
|
| 16 |
195th ENMC International Workshop: Newborn screening for Duchenne muscular dystrophy 14–16th December, 2012, Naarden, The Netherlands
|
Ellis, Juliet A.
|
|
2013
|
23 |
8 |
p. 682-689
8 p.
|
artikel
|
| 17 |
Transforming Duchenne Care: Meeting 25–26 June 2012, Ft. Lauderdale, Florida, USA
|
Kinnett, Kathi
|
|
2013
|
23 |
8 |
p. 690-695
6 p.
|
artikel
|
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