| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acknowledgements
|
|
|
|
179 |
1-2 |
p. 1-2
|
artikel
|
| 2 |
Contents
|
|
|
|
179 |
1-2 |
p. v-vi
|
artikel
|
| 3 |
Contribution of muscle MRI for diagnosis of myopathy
|
Venturelli, N.
|
|
|
179 |
1-2 |
p. 61-80
|
artikel
|
| 4 |
Current treatments of spinal muscular atrophy in adults
|
Cintas, P.
|
|
|
179 |
1-2 |
p. 106-113
|
artikel
|
| 5 |
Editorial Board
|
|
|
|
179 |
1-2 |
p. i
|
artikel
|
| 6 |
Entrapment partly participates in the longitudinal progression of neuropathy with anti-MAG antibodies
|
Ohara, M.
|
|
|
179 |
1-2 |
p. 118-122
|
artikel
|
| 7 |
Gene therapy review: Duchenne muscular dystrophy case study
|
Berling, E.
|
|
|
179 |
1-2 |
p. 90-105
|
artikel
|
| 8 |
Progress in hereditary neuropathies, myopathies and motoneuron disorders!
|
Camdessanché, J.-P.
|
|
|
179 |
1-2 |
p. 3-4
|
artikel
|
| 9 |
Strategy for genetic analysis in hereditary neuropathy
|
Masingue, M.
|
|
|
179 |
1-2 |
p. 10-29
|
artikel
|
| 10 |
The new horizons for treatment of Late-Onset Pompe Disease (LOPD)
|
Guémy, C.
|
|
|
179 |
1-2 |
p. 81-89
|
artikel
|
| 11 |
Therapeutic tools for familial ALS
|
Camu, W.
|
|
|
179 |
1-2 |
p. 49-53
|
artikel
|
| 12 |
Therapeutic tools for inherited neuropathies
|
Péréon, Y.
|
|
|
179 |
1-2 |
p. 5-9
|
artikel
|
| 13 |
Treating hereditary transthyretin amyloidosis: Present & future challenges
|
Echaniz-Laguna, A.
|
|
|
179 |
1-2 |
p. 30-34
|
artikel
|
| 14 |
Treatment of Charcot-Marie-Tooth neuropathies
|
Beloribi-Djefaflia, S.
|
|
|
179 |
1-2 |
p. 35-48
|
artikel
|
| 15 |
Treatment of hereditary amyotrophic lateral sclerosis
|
Corcia, P.
|
|
|
179 |
1-2 |
p. 54-60
|
artikel
|
| 16 |
Wasted leg syndrome: An atypical slowly-progressive form of lower motor neuron disease
|
Schön, M.
|
|
|
179 |
1-2 |
p. 114-117
|
artikel
|
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