| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Clinical Cases in Neurology
|
Buckley, Camilla
|
|
2003
|
13 |
3 |
p. 264-
1 p.
|
article
|
| 2 |
Congenital myasthenic syndrome due to a novel missense mutation in the gene encoding choline acetyltransferase
|
Schmidt, Carolin
|
|
2003
|
13 |
3 |
p. 245-251
7 p.
|
article
|
| 3 |
Congenital myasthenic syndromes: gene mutations
|
|
|
2003
|
13 |
3 |
p. 283-285
3 p.
|
article
|
| 4 |
Contemporary Treatments in Neurology
|
Wroe, Stephen J.
|
|
2003
|
13 |
3 |
p. 263-
1 p.
|
article
|
| 5 |
Editorial Board
|
|
|
2003
|
13 |
3 |
p. IFC-
1 p.
|
article
|
| 6 |
Genetics of Movement Disorders
|
Emery, Alan
|
|
2003
|
13 |
3 |
p. 264-265
2 p.
|
article
|
| 7 |
Increased mitochondrial processing intermediates associated with three tRNALeu(UUR) gene mutations
|
Koga, Atsuko
|
|
2003
|
13 |
3 |
p. 259-262
4 p.
|
article
|
| 8 |
Instructions to authors
|
|
|
2003
|
13 |
3 |
p. 286-287
2 p.
|
article
|
| 9 |
Laminin α2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice
|
Guo, L.T.
|
|
2003
|
13 |
3 |
p. 207-215
9 p.
|
article
|
| 10 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
2003
|
13 |
3 |
p. 277-282
6 p.
|
article
|
| 11 |
Neuromuscular disorders: gene location
|
|
|
2003
|
13 |
3 |
p. 266-276
11 p.
|
article
|
| 12 |
Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in γ-sarcoglycan-deficient mice
|
Sasaoka, Toshikuni
|
|
2003
|
13 |
3 |
p. 193-206
14 p.
|
article
|
| 13 |
Persistent over-expression of specific CC class chemokines correlates with macrophage and T-cell recruitment in mdx skeletal muscle
|
Porter, John D.
|
|
2003
|
13 |
3 |
p. 223-235
13 p.
|
article
|
| 14 |
Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations
|
Dalakas, Marinos C.
|
|
2003
|
13 |
3 |
p. 252-258
7 p.
|
article
|
| 15 |
Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene
|
Besse, Sylvie
|
|
2003
|
13 |
3 |
p. 216-222
7 p.
|
article
|
| 16 |
The Autonomic Nervous System in Health and Disease
|
Harkness, Kirsty
|
|
2003
|
13 |
3 |
p. 263-264
2 p.
|
article
|
| 17 |
Two novel mutations in the COLQ gene cause endplate acetylcholinesterase deficiency
|
Ishigaki, Keiko
|
|
2003
|
13 |
3 |
p. 236-244
9 p.
|
article
|
Journal description