nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Clinical Cases in Neurology
|
Buckley, Camilla |
|
2003 |
13 |
3 |
p. 264- 1 p. |
artikel |
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. |
artikel |
3 |
Congenital myasthenic syndromes: gene mutations
|
|
|
2003 |
13 |
3 |
p. 283-285 3 p. |
artikel |
4 |
Contemporary Treatments in Neurology
|
Wroe, Stephen J. |
|
2003 |
13 |
3 |
p. 263- 1 p. |
artikel |
5 |
Editorial Board
|
|
|
2003 |
13 |
3 |
p. IFC- 1 p. |
artikel |
6 |
Genetics of Movement Disorders
|
Emery, Alan |
|
2003 |
13 |
3 |
p. 264-265 2 p. |
artikel |
7 |
Increased mitochondrial processing intermediates associated with three tRNALeu(UUR) gene mutations
|
Koga, Atsuko |
|
2003 |
13 |
3 |
p. 259-262 4 p. |
artikel |
8 |
Instructions to authors
|
|
|
2003 |
13 |
3 |
p. 286-287 2 p. |
artikel |
9 |
Laminin α2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice
|
Guo, L.T. |
|
2003 |
13 |
3 |
p. 207-215 9 p. |
artikel |
10 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
2003 |
13 |
3 |
p. 277-282 6 p. |
artikel |
11 |
Neuromuscular disorders: gene location
|
|
|
2003 |
13 |
3 |
p. 266-276 11 p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
16 |
The Autonomic Nervous System in Health and Disease
|
Harkness, Kirsty |
|
2003 |
13 |
3 |
p. 263-264 2 p. |
artikel |
17 |
Two novel mutations in the COLQ gene cause endplate acetylcholinesterase deficiency
|
Ishigaki, Keiko |
|
2003 |
13 |
3 |
p. 236-244 9 p. |
artikel |