| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Announcements: Emery and Meyron Lectures
|
|
|
2007
|
17 |
3 |
p. VI-
1 p.
|
artikel
|
| 2 |
Announcement: 10th Summer School of Myology
|
|
|
2007
|
17 |
3 |
p. VII-
1 p.
|
artikel
|
| 3 |
Announcement: Update in Neuromuscular Disorders
|
|
|
2007
|
17 |
3 |
p. V-
1 p.
|
artikel
|
| 4 |
Ascorbic acid inhibits PMP22 expression by reducing cAMP levels
|
Kaya, Ferdinand
|
|
2007
|
17 |
3 |
p. 248-253
6 p.
|
artikel
|
| 5 |
Contents
|
|
|
2007
|
17 |
3 |
p. OBC-
1 p.
|
artikel
|
| 6 |
Different pattern of HSP47 expression in skeletal muscle of patients with neuromuscular diseases
|
Higuchi, Itsuro
|
|
2007
|
17 |
3 |
p. 221-226
6 p.
|
artikel
|
| 7 |
Forthcoming Meetings
|
|
|
2007
|
17 |
3 |
p. VIII-IX
nvt p.
|
artikel
|
| 8 |
IFC: Editorial Board
|
|
|
2007
|
17 |
3 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Instructions to Authors
|
|
|
2007
|
17 |
3 |
p. 272-273
2 p.
|
artikel
|
| 10 |
Molecular characterization of myophosphorylase deficiency (McArdle disease) in 34 patients from Southern France: Identification of 10 new mutations. Absence of genotype–phenotype correlation
|
Aquaron, Robert
|
|
2007
|
17 |
3 |
p. 235-241
7 p.
|
artikel
|
| 11 |
Myotubular Trust
|
|
|
2007
|
17 |
3 |
p. 271-
1 p.
|
artikel
|
| 12 |
[No title]
|
Squier, Waney
|
|
2007
|
17 |
3 |
p. 267-
1 p.
|
artikel
|
| 13 |
[No title]
|
Hilton-Jones, David
|
|
2007
|
17 |
3 |
p. 267-268
2 p.
|
artikel
|
| 14 |
[No title]
|
Rose, Michael
|
|
2007
|
17 |
3 |
p. 268-
1 p.
|
artikel
|
| 15 |
Novel COLQ mutation 950delC in synaptic congenital myasthenic syndrome and symptomatic heterozygous relatives
|
Schreiner, Felix
|
|
2007
|
17 |
3 |
p. 262-265
4 p.
|
artikel
|
| 16 |
Postnatal overexpression of the CT GalNAc transferase inhibits muscular dystrophy in mdx mice without altering muscle growth or neuromuscular development: Evidence for a utrophin-independent mechanism
|
Xu, Rui
|
|
2007
|
17 |
3 |
p. 209-220
12 p.
|
artikel
|
| 17 |
Ribonuclear foci at the neuromuscular junction in myotonic dystrophy type 1
|
Wheeler, T.M.
|
|
2007
|
17 |
3 |
p. 242-247
6 p.
|
artikel
|
| 18 |
Samba steps for pre-clinical tests of drug therapy in Duchenne Muscular Dystrophy
|
|
|
2007
|
17 |
3 |
p. 269-
1 p.
|
artikel
|
| 19 |
Serial casting of the ankles in Duchenne muscular dystrophy: can it be an alternative to surgery?
|
Main, Marion
|
|
2007
|
17 |
3 |
p. 227-230
4 p.
|
artikel
|
| 20 |
Severe encephalomyopathy in a patient with homoplasmic A5814G point mutation in mitochondrial tRNACys gene
|
Scuderi, Carmela
|
|
2007
|
17 |
3 |
p. 258-261
4 p.
|
artikel
|
| 21 |
Siblings with recessive oculopharyngeal muscular dystrophy
|
Hebbar, Srisha
|
|
2007
|
17 |
3 |
p. 254-257
4 p.
|
artikel
|
| 22 |
Skeletal dysplasia presenting as a neuromuscular disorder – report of three children
|
Bondestam, Jonas
|
|
2007
|
17 |
3 |
p. 231-234
4 p.
|
artikel
|
| 23 |
The allure of stem cell therapy for muscular dystrophy
|
Grounds, Miranda D.
|
|
2007
|
17 |
3 |
p. 206-208
3 p.
|
artikel
|
| 24 |
Too much hype, not enough hope: Are balanced reporting and proper controls too much to expect from therapeutic studies in animal models of neuromuscular diseases that presage clinical trials in humans?
|
Bretag, Allan
|
|
2007
|
17 |
3 |
p. 203-205
3 p.
|
artikel
|
| 25 |
TREAT-NMD
|
|
|
2007
|
17 |
3 |
p. 270-271
2 p.
|
artikel
|
| 26 |
Underdiagnosis of X-linked myotubular myopathy and other forms of centronuclear myopathy
|
Foye, Patrick M.
|
|
2007
|
17 |
3 |
p. 266-
1 p.
|
artikel
|
| 27 |
WMS12 Announcement
|
|
|
2007
|
17 |
3 |
p. III-
1 p.
|
artikel
|
| 28 |
WMS: Application Form
|
|
|
2007
|
17 |
3 |
p. I-
1 p.
|
artikel
|
| 29 |
WMS: Executive Board Announcement
|
|
|
2007
|
17 |
3 |
p. IV-
1 p.
|
artikel
|
| 30 |
WMS: Web addresses
|
|
|
2007
|
17 |
3 |
p. II-
1 p.
|
artikel
|
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