| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An unusual presentation of Muscle–Eye–Brain disease: Severe eye abnormalities with mild muscle and brain involvement
|
Demir, Ercan
|
|
2009
|
19 |
10 |
p. 692-695
4 p.
|
artikel
|
| 2 |
A TPM3 mutation causing cap myopathy
|
De Paula, Andre Maues
|
|
2009
|
19 |
10 |
p. 685-688
4 p.
|
artikel
|
| 3 |
Congenital monomelic muscular hypertrophy of the upper extremity
|
Gilhuis, H. Jacobus
|
|
2009
|
19 |
10 |
p. 714-717
4 p.
|
artikel
|
| 4 |
Dysphagia in X-linked bulbospinal muscular atrophy (Kennedy disease)
|
Warnecke, Tobias
|
|
2009
|
19 |
10 |
p. 704-708
5 p.
|
artikel
|
| 5 |
Editorial Board
|
|
|
2009
|
19 |
10 |
p. IFC-
1 p.
|
artikel
|
| 6 |
Facilitating family adjustment to a diagnosis of Duchenne muscular dystrophy: April 24–25, 2008, Miami, Florida
|
Poysky, James
|
|
2009
|
19 |
10 |
p. 733-738
6 p.
|
artikel
|
| 7 |
First genomic rearrangement of the RYR1 gene associated with an atypical presentation of lethal neonatal hypotonia
|
Monnier, Nicole
|
|
2009
|
19 |
10 |
p. 680-684
5 p.
|
artikel
|
| 8 |
Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosis
|
Luquin, Natasha
|
|
2009
|
19 |
10 |
p. 696-700
5 p.
|
artikel
|
| 9 |
Hereditary motor and sensory neuropathy caused by a novel mutation in LITAF
|
Gerding, Wanda Maria
|
|
2009
|
19 |
10 |
p. 701-703
3 p.
|
artikel
|
| 10 |
Muscle MRI in FHL1-linked reducing body myopathy
|
Astrea, G.
|
|
2009
|
19 |
10 |
p. 689-691
3 p.
|
artikel
|
| 11 |
On the spectrum of leprosy neuropathies: Multifocal inflammatory neuropathy heralding leprosy relapse
|
Gondim, Francisco de Assis A.
|
|
2009
|
19 |
10 |
p. 711-713
3 p.
|
artikel
|
| 12 |
Posterior reversible encephalopathy as the initial manifestation of a Guillain–Barré syndrome
|
Sutter, R.
|
|
2009
|
19 |
10 |
p. 709-710
2 p.
|
artikel
|
| 13 |
Relapse of POEMS syndrome without increased level of VEGF
|
Kuwabara, Satoshi
|
|
2009
|
19 |
10 |
p. 740-
1 p.
|
artikel
|
| 14 |
Response
|
Imai, Noboru
|
|
2009
|
19 |
10 |
p. 740-741
2 p.
|
artikel
|
| 15 |
Rhabdomyolysis caused by tocolytic therapy with ritodrine hydrochloride
|
Verriello, L.
|
|
2009
|
19 |
10 |
p. 718-720
3 p.
|
artikel
|
| 16 |
164th ENMC International workshop: 6th workshop on centronuclear (myotubular) myopathies, 16–18th January 2009, Naarden, The Netherlands
|
Jungbluth, Heinz
|
|
2009
|
19 |
10 |
p. 721-729
9 p.
|
artikel
|
| 17 |
The potential of inducing systemic and therapeutic exon skipping with oligonucleotides evaluated in the Beagle dog with Muscular Dystrophy
|
|
|
2009
|
19 |
10 |
p. 739-
1 p.
|
artikel
|
| 18 |
What we do not know about pregnancy in hereditary neuromuscular disorders
|
Argov, Zohar
|
|
2009
|
19 |
10 |
p. 675-679
5 p.
|
artikel
|
| 19 |
WMS 2010
|
|
|
2009
|
19 |
10 |
p. I-
1 p.
|
artikel
|
| 20 |
WMS News
|
|
|
2009
|
19 |
10 |
p. III-IV
nvt p.
|
artikel
|
| 21 |
WMS online application form
|
|
|
2009
|
19 |
10 |
p. II-
1 p.
|
artikel
|
| 22 |
Workshop on the use of stimulation single fibre electromyography for the diagnosis of myasthenic syndromes in children held in the Institute of Child Health and Great Ormond Street Hospital for Children in London on April 24th, 2009
|
Pitt, Matthew
|
|
2009
|
19 |
10 |
p. 730-732
3 p.
|
artikel
|
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