| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adult Polyglucosan Body Disease: Clinical and histological heterogeneity of a large Italian family
|
Colombo, I.
|
|
2015
|
25 |
5 |
p. 423-428
6 p.
|
artikel
|
| 2 |
A normal life without muscle dystrophin
|
Zatz, M.
|
|
2015
|
25 |
5 |
p. 371-374
4 p.
|
artikel
|
| 3 |
A novel large deletion in the RYR1 gene in a Belgian family with late-onset and recessive core myopathy
|
Remiche, Gauthier
|
|
2015
|
25 |
5 |
p. 397-402
6 p.
|
artikel
|
| 4 |
BAG3 myofibrillar myopathy presenting with cardiomyopathy
|
Konersman, Chamindra G.
|
|
2015
|
25 |
5 |
p. 418-422
5 p.
|
artikel
|
| 5 |
Dystrophin and Duchenne dystrophy
|
Dubowitz, Victor
|
|
2015
|
25 |
5 |
p. 361-362
2 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2015
|
25 |
5 |
p. CO2-
1 p.
|
artikel
|
| 7 |
Evaluation of the serum matrix metalloproteinase-9 as a biomarker for monitoring disease progression in Duchenne muscular dystrophy
|
Zocevic, Aleksandar
|
|
2015
|
25 |
5 |
p. 444-446
3 p.
|
artikel
|
| 8 |
Lack of correlation between the ventilatory response to CO2 and lung function impairment in myotonic dystrophy patients: Evidence for a dysregulation at central level
|
Poussel, Mathias
|
|
2015
|
25 |
5 |
p. 403-408
6 p.
|
artikel
|
| 9 |
Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin
|
Castro-Gago, Manuel
|
|
2015
|
25 |
5 |
p. 443-
1 p.
|
artikel
|
| 10 |
Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype
|
Vieira, Natassia M.
|
|
2015
|
25 |
5 |
p. 363-370
8 p.
|
artikel
|
| 11 |
PLEC1 mutation associated with left ventricular hypertrabeculation/noncompaction
|
Finsterer, Josef
|
|
2015
|
25 |
5 |
p. 447-448
2 p.
|
artikel
|
| 12 |
Progression and variation of fatty infiltration of the thigh muscles in Duchenne muscular dystrophy, a muscle magnetic resonance imaging study
|
Li, Wenzhu
|
|
2015
|
25 |
5 |
p. 375-380
6 p.
|
artikel
|
| 13 |
Renal function in children and adolescents with Duchenne muscular dystrophy
|
Braat, Elke
|
|
2015
|
25 |
5 |
p. 381-387
7 p.
|
artikel
|
| 14 |
Response to: Evaluation of the serum matrix metalloproteinase-9 as a biomarker for monitoring disease progression in Duchenne muscular dystrophy
|
Spitali, Pietro
|
|
2015
|
25 |
5 |
p. 446-447
2 p.
|
artikel
|
| 15 |
Response to: Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin
|
Zatz, Mayana
|
|
2015
|
25 |
5 |
p. 444-
1 p.
|
artikel
|
| 16 |
Response to: PLEC1 mutation associated with left ventricular hypertrabeculation/noncompaction
|
Villa, Chet R.
|
|
2015
|
25 |
5 |
p. 448-449
2 p.
|
artikel
|
| 17 |
Skin features in myotonic dystrophy type 1: An observational study
|
Campanati, A.
|
|
2015
|
25 |
5 |
p. 409-413
5 p.
|
artikel
|
| 18 |
Surgical treatment of obesity in DM1 – a case report and a review of the literature
|
Håkansson, K.
|
|
2015
|
25 |
5 |
p. 414-417
4 p.
|
artikel
|
| 19 |
207th ENMC Workshop on chronic respiratory insufficiency in myotonic dystrophies: Management and implications for research, 27–29 June 2014, Naarden, The Netherlands
|
Sansone, V.A.
|
|
2015
|
25 |
5 |
p. 432-442
11 p.
|
artikel
|
| 20 |
Treatment of myasthenia gravis with dropped head: A report of 2 cases and review of the literature
|
Tamai, Michihiro
|
|
2015
|
25 |
5 |
p. 429-431
3 p.
|
artikel
|
| 21 |
Two novel nebulin variants in an adult patient with congenital nemaline myopathy
|
Güttsches, Anne K.
|
|
2015
|
25 |
5 |
p. 392-396
5 p.
|
artikel
|
| 22 |
Zebra body myopathy is caused by a mutation in the skeletal muscle actin gene (ACTA1)
|
Sewry, C.A.
|
|
2015
|
25 |
5 |
p. 388-391
4 p.
|
artikel
|
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