nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Abstracts
|
|
|
2003 |
13 |
7-8 |
p. 615-668 54 p. |
artikel |
2 |
Abstracts
|
|
|
2003 |
13 |
7-8 |
p. 669-673 5 p. |
artikel |
3 |
Abstracts
|
|
|
2003 |
13 |
7-8 |
p. 597- 1 p. |
artikel |
4 |
A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia
|
Deschauer, Marcus |
|
2003 |
13 |
7-8 |
p. 568-572 5 p. |
artikel |
5 |
Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes
|
Watts, Giles D.J |
|
2003 |
13 |
7-8 |
p. 559-567 9 p. |
artikel |
6 |
Editorial Board
|
|
|
2003 |
13 |
7-8 |
p. IFC- 1 p. |
artikel |
7 |
Evaluation of muscle glycogen content by 13C NMR spectroscopy in adult-onset acid maltase deficiency
|
Wary, Claire |
|
2003 |
13 |
7-8 |
p. 545-553 9 p. |
artikel |
8 |
Gene table
|
|
|
2003 |
13 |
7-8 |
p. 691-695 5 p. |
artikel |
9 |
Gene table
|
|
|
2003 |
13 |
7-8 |
p. 674-684 11 p. |
artikel |
10 |
Gene table
|
|
|
2003 |
13 |
7-8 |
p. 685-690 6 p. |
artikel |
11 |
Instructions to Authors
|
|
|
2003 |
13 |
7-8 |
p. 696-697 2 p. |
artikel |
12 |
Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1)
|
Sparrow, John C. |
|
2003 |
13 |
7-8 |
p. 519-531 13 p. |
artikel |
13 |
Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotype
|
Mercuri, E |
|
2003 |
13 |
7-8 |
p. 554-558 5 p. |
artikel |
14 |
Programme
|
|
|
2003 |
13 |
7-8 |
p. 603-613 11 p. |
artikel |
15 |
Programme
|
|
|
2003 |
13 |
7-8 |
p. 600-602 3 p. |
artikel |
16 |
Report of the 115th ENMC workshop: DM2/PROMM and other myotonic dystrophies
|
Udd, B |
|
2003 |
13 |
7-8 |
p. 589-596 8 p. |
artikel |
17 |
Table of location of Abstract topics
|
|
|
2003 |
13 |
7-8 |
p. 614- 1 p. |
artikel |
18 |
The 10 autosomal recessive limb-girdle muscular dystrophies
|
Zatz, Mayana |
|
2003 |
13 |
7-8 |
p. 532-544 13 p. |
artikel |
19 |
114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17–19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE)
|
Muntoni, F |
|
2003 |
13 |
7-8 |
p. 579-588 10 p. |
artikel |
20 |
110th ENMC International Workshop: The congenital cranial dysinnervation disorders (CCDDs)
|
Gutowski, N.J |
|
2003 |
13 |
7-8 |
p. 573-578 6 p. |
artikel |
21 |
Welcome to Szeged
|
|
|
2003 |
13 |
7-8 |
p. 598-599 2 p. |
artikel |