| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO)
|
Berardo, Andres
|
|
2010
|
20 |
3 |
p. 204-206
3 p.
|
artikel
|
| 2 |
A pioneer in neuropathology: Alix Joffroy (1844–1908), J.-M Charcot’s pupil
|
Tiberghien, D.
|
|
2010
|
20 |
3 |
p. 207-213
7 p.
|
artikel
|
| 3 |
Autoantibody profiles in two patients with non-autoimmune muscle disease implicate a role for gliadin autoreactivity
|
Olsen, Nancy J.
|
|
2010
|
20 |
3 |
p. 188-191
4 p.
|
artikel
|
| 4 |
Commentary 2 on “Motoneuron transplantation rescues the phenotype of SMARD1
|
|
|
2010
|
20 |
3 |
p. 214-215
2 p.
|
artikel
|
| 5 |
Desmin myopathy with severe cardiomyopathy in a Uruguayan family due to a codon deletion in a new location within the desmin 1A rod domain
|
Vernengo, Luis
|
|
2010
|
20 |
3 |
p. 178-187
10 p.
|
artikel
|
| 6 |
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery–Dreifuss muscular dystrophy
|
Nigro, Gerardo
|
|
2010
|
20 |
3 |
p. 174-177
4 p.
|
artikel
|
| 7 |
Editorial Board
|
|
|
2010
|
20 |
3 |
p. IFC-
1 p.
|
artikel
|
| 8 |
ENMC Assessment
|
|
|
2010
|
20 |
3 |
p. V-
1 p.
|
artikel
|
| 9 |
Letter 2
|
Buccella, Filippo
|
|
2010
|
20 |
3 |
p. 216-217
2 p.
|
artikel
|
| 10 |
Letter 3
|
Quinlivan, Ros
|
|
2010
|
20 |
3 |
p. 217-
1 p.
|
artikel
|
| 11 |
Letter 1
|
Munn, Michael W.
|
|
2010
|
20 |
3 |
p. 216-
1 p.
|
artikel
|
| 12 |
Letter 4
|
Tseng, Brian
|
|
2010
|
20 |
3 |
p. 217-
1 p.
|
artikel
|
| 13 |
Letter 7
|
Dubowitz, Victor
|
|
2010
|
20 |
3 |
p. 218-219
2 p.
|
artikel
|
| 14 |
Letter 5
|
Wong, Brenda L.
|
|
2010
|
20 |
3 |
p. 217-218
2 p.
|
artikel
|
| 15 |
Letter 6
|
Topaloglu, Haluk
|
|
2010
|
20 |
3 |
p. 218-
1 p.
|
artikel
|
| 16 |
Microvasculopathic neuromuscular diseases: Lessons from hypoxia-inducible factors
|
Probst-Cousin, Stefan
|
|
2010
|
20 |
3 |
p. 192-197
6 p.
|
artikel
|
| 17 |
Motoneuron transplantation rescues the phenotype of SMARD1 (spinal muscular atrophy with respiratory distress type 1). J Neuroscience 2009; 29: 11761–11771
|
|
|
2010
|
20 |
3 |
p. 214-
1 p.
|
artikel
|
| 18 |
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
|
Zhou, Haiyan
|
|
2010
|
20 |
3 |
p. 166-173
8 p.
|
artikel
|
| 19 |
[No title]
|
Jungbluth, Heinz
|
|
2010
|
20 |
3 |
p. 222-
1 p.
|
artikel
|
| 20 |
[No title]
|
Wills, Adrian
|
|
2010
|
20 |
3 |
p. 222-
1 p.
|
artikel
|
| 21 |
Parent project
|
|
|
2010
|
20 |
3 |
p. VI-
1 p.
|
artikel
|
| 22 |
Reliability of telephone administration of the PedsQL™ Generic Quality of Life Inventory™ and Neuromuscular Module™ in spinal muscular atrophy (SMA)
|
Dunaway, Sally
|
|
2010
|
20 |
3 |
p. 162-165
4 p.
|
artikel
|
| 23 |
Richard H.T. Edwards PhD, FRCP (1939–2009)
|
Dubowitz, Victor
|
|
2010
|
20 |
3 |
p. 220-221
2 p.
|
artikel
|
| 24 |
The Children’s Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND): Test development and reliability
|
Glanzman, A.M.
|
|
2010
|
20 |
3 |
p. 155-161
7 p.
|
artikel
|
| 25 |
Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion
|
Lesko, Nicole
|
|
2010
|
20 |
3 |
p. 198-203
6 p.
|
artikel
|
| 26 |
WMS 2010
|
|
|
2010
|
20 |
3 |
p. I-
1 p.
|
artikel
|
| 27 |
WMS News
|
|
|
2010
|
20 |
3 |
p. III-IV
nvt p.
|
artikel
|
| 28 |
WMS online application form
|
|
|
2010
|
20 |
3 |
p. II-
1 p.
|
artikel
|
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