| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy
|
Conforti, F.L.
|
|
2008
|
18 |
1 |
p. 68-70
3 p.
|
artikel
|
| 2 |
Commentary from the Editor
|
Dubowitz, Victor
|
|
2008
|
18 |
1 |
p. 1-5
5 p.
|
artikel
|
| 3 |
Congenital hypomyelinating neuropathy, a long term follow-up study in an affected family
|
Smit, Liesbeth S.
|
|
2008
|
18 |
1 |
p. 59-62
4 p.
|
artikel
|
| 4 |
Editorial Board
|
|
|
2008
|
18 |
1 |
p. IFC-
1 p.
|
artikel
|
| 5 |
Foreword to Gene Table
|
|
|
2008
|
18 |
1 |
p. 99-100
2 p.
|
artikel
|
| 6 |
Forthcoming meetings
|
|
|
2008
|
18 |
1 |
p. XI-
1 p.
|
artikel
|
| 7 |
Gene table of monogenic neuromuscular disorder (nuclear genome only)
|
|
|
2008
|
18 |
1 |
p. 101-129
29 p.
|
artikel
|
| 8 |
Histone H1 is released from myonuclei and present in rimmed vacuoles with DNA in inclusion body myositis
|
Nakano, Satoshi
|
|
2008
|
18 |
1 |
p. 27-33
7 p.
|
artikel
|
| 9 |
Limb–girdle muscular dystrophy: Diagnostic evaluation, frequency and clues to pathogenesis
|
Lo, Harriet P.
|
|
2008
|
18 |
1 |
p. 34-44
11 p.
|
artikel
|
| 10 |
Mesenchymal stem cells from umbilical cord: Do not discard the cord!
|
Secco, Mariane
|
|
2008
|
18 |
1 |
p. 17-18
2 p.
|
artikel
|
| 11 |
Myoglobinuria in boys with Duchenne muscular dystrophy on corticosteroid therapy
|
Garrood, P.
|
|
2008
|
18 |
1 |
p. 71-73
3 p.
|
artikel
|
| 12 |
Myopathy associated with statin therapy
|
Hilton-Jones, David
|
|
2008
|
18 |
1 |
p. 97-98
2 p.
|
artikel
|
| 13 |
Other forms of survival motor neuron protein and spinal muscular atrophy: An opinion
|
|
|
2008
|
18 |
1 |
p. 82-83
2 p.
|
artikel
|
| 14 |
Protein O-mannosyltransferase activities in lymphoblasts from patients with α-dystroglycanopathies
|
Manya, Hiroshi
|
|
2008
|
18 |
1 |
p. 45-51
7 p.
|
artikel
|
| 15 |
Reduced expression of Kir6.2/SUR2A subunits explains KATP deficiency in K+-depleted rats
|
Tricarico, Domenico
|
|
2008
|
18 |
1 |
p. 74-80
7 p.
|
artikel
|
| 16 |
Reliability of clinical outcome measures in Charcot-Marie-Tooth disease
|
Solari, A.
|
|
2008
|
18 |
1 |
p. 19-26
8 p.
|
artikel
|
| 17 |
Rhabdomyolysis in pontocerebellar hypoplasia type 2 (PCH-2)
|
Barth, Peter G.
|
|
2008
|
18 |
1 |
p. 52-58
7 p.
|
artikel
|
| 18 |
Spinal muscular atrophy: Motoneurone or muscle disease?
|
|
|
2008
|
18 |
1 |
p. 81-82
2 p.
|
artikel
|
| 19 |
Sporadic inclusion body myositis: a continuing puzzle
|
Needham, M.
|
|
2008
|
18 |
1 |
p. 6-16
11 p.
|
artikel
|
| 20 |
151st ENMC International Workshop: Inflammatory Neuropathy Consortium 13th–15th April 2007, Schiphol, The Netherlands
|
Lunn, M.P.
|
|
2008
|
18 |
1 |
p. 85-89
5 p.
|
artikel
|
| 21 |
Substantial immune suppression required in gene therapy for muscular dystrophy?
|
|
|
2008
|
18 |
1 |
p. 83-84
2 p.
|
artikel
|
| 22 |
The m.5650G>A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathy
|
McFarland, Robert
|
|
2008
|
18 |
1 |
p. 63-67
5 p.
|
artikel
|
| 23 |
147th ENMC International Workshop: Guideline on processing and evaluation of sural nerve biopsies, 15–17 December 2006, Naarden, The Netherlands
|
Sommer, C.
|
|
2008
|
18 |
1 |
p. 90-96
7 p.
|
artikel
|
| 24 |
WMS online application
|
|
|
2008
|
18 |
1 |
p. IX-
1 p.
|
artikel
|
| 25 |
WMS12 Sicily: Scientific and Social Invasion
|
|
|
2008
|
18 |
1 |
p. I-V
nvt p.
|
artikel
|
| 26 |
WMS - 13th International Congress
|
|
|
2008
|
18 |
1 |
p. X-
1 p.
|
artikel
|
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