nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndrome
|
Müller, Juliane S. |
|
2004 |
14 |
11 |
p. 744-749 6 p. |
artikel |
2 |
Characteristics of the increase in plasma brain natriuretic peptide level in left ventricular systolic dysfunction, associated with muscular dystrophy in comparison with idiopathic dilated cardiomyopathy
|
Demachi, Jun |
|
2004 |
14 |
11 |
p. 732-739 8 p. |
artikel |
3 |
Expression profiling in spinal muscular atrophy reveals an RNA binding protein deficit
|
Anderson, Kirstie N. |
|
2004 |
14 |
11 |
p. 711-722 12 p. |
artikel |
4 |
Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy
|
Passamonti, Luca |
|
2004 |
14 |
11 |
p. 705-710 6 p. |
artikel |
5 |
IFC: Editorial Board
|
|
|
2004 |
14 |
11 |
p. IFC- 1 p. |
artikel |
6 |
Instructions to Authors
|
|
|
2004 |
14 |
11 |
p. 776-777 2 p. |
artikel |
7 |
Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNASer(UCN) gene
|
Fetoni, Vincenza |
|
2004 |
14 |
11 |
p. 723-726 4 p. |
artikel |
8 |
Mutation screening in Korean hypokalemic periodic paralysis patients: a novel SCN4A Arg672Cys mutation
|
Kim, Myeong-Kyu |
|
2004 |
14 |
11 |
p. 727-731 5 p. |
artikel |
9 |
Myositis in infiltrative lymphocytosis syndrome: clinicopathological observations and treatment
|
Attarian, S. |
|
2004 |
14 |
11 |
p. 740-743 4 p. |
artikel |
10 |
[No title]
|
Orrell, Richard W. |
|
2004 |
14 |
11 |
p. 775- 1 p. |
artikel |
11 |
[No title]
|
Kennett, Robin |
|
2004 |
14 |
11 |
p. 774- 1 p. |
artikel |
12 |
121st ENMC International Workshop on Desmin and Protein Aggregate Myopathies. 7–9 November 2003, Naarden, The Netherlands
|
Goebel, HansH. |
|
2004 |
14 |
11 |
p. 767-773 7 p. |
artikel |
13 |
111th ENMC International Workshop on Multi-minicore Disease. 2nd International MmD Workshop, 9–11 November 2002, Naarden, The Netherlands
|
Jungbluth, Heinz |
|
2004 |
14 |
11 |
p. 754-766 13 p. |
artikel |
14 |
Two novel mutations in the spastin gene (SPG4) found by DHPLC mutation analysis
|
Falco, Michele |
|
2004 |
14 |
11 |
p. 750-753 4 p. |
artikel |