Digital Library
Close Browse articles from a journal
     Journal description
       All volumes of the corresponding journal
         All issues of the corresponding volume
                                       All articles of the corresponding issues
 
                             19 results found
no title author magazine year volume issue page(s) type
1 Analysis of growth factor expression in affected and unaffected muscles of oculo-pharyngeal muscular dystrophy (OPMD) patients: A pilot study Bouazza, Belaid
2009
19 3 p. 199-206
8 p.
article
2 Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin gene Baskin, Berivan
2009
19 3 p. 189-192
4 p.
article
3 Does the K153R variant of the myostatin gene influence the clinical presentation of women with McArdle disease? González-Freire, Marta
2009
19 3 p. 220-222
3 p.
article
4 Dysphagia is present but mild in myotonic dystrophy type 2 Tieleman, A.A.
2009
19 3 p. 196-198
3 p.
article
5 Editorial Board 2009
19 3 p. IFC-
1 p.
article
6 ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency Liang, Wen-Chen
2009
19 3 p. 212-216
5 p.
article
7 Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotype Vuillaumier-Barrot, S.
2009
19 3 p. 182-188
7 p.
article
8 Glucocorticoids may trigger attacks in several types of periodic paralysis Arzel-Hézode, Marianne
2009
19 3 p. 217-219
3 p.
article
9 Immune-mediated rippling muscle disease with myasthenia gravis: A report of seven patients with long-term follow-up in two Schoser, Benedikt
2009
19 3 p. 223-228
6 p.
article
10 Interfamilial phenotypic heterogeneity in SMARD1 Joseph, S.
2009
19 3 p. 193-195
3 p.
article
11 Muscle course 2009 2009
19 3 p. I-
1 p.
article
12 Myopathic form of phosphoglycerate kinase (PGK) deficiency: A new case and pathogenic considerations Spiegel, Ronen
2009
19 3 p. 207-211
5 p.
article
13 Nemaline myopathy: A tale of two cultures Dubowitz, Victor
2009
19 3 p. 177-178
2 p.
article
14 Newcastle: From coal to muscle 2009
19 3 p. 235-239
5 p.
article
15 The exon 55 deletion in the nebulin gene – One single founder mutation with world-wide occurrence Lehtokari, Vilma-Lotta
2009
19 3 p. 179-181
3 p.
article
16 158th ENMC international workshop on congenital muscular dystrophy (Xth international CMD workshop) 8th–10th February 2008 Naarden, The Netherlands Muntoni, F.
2009
19 3 p. 229-234
6 p.
article
17 WMS 2009 2009
19 3 p. II-
1 p.
article
18 WMS News 2009
19 3 p. IV-V
nvt p.
article
19 WMS online application form 2009
19 3 p. III-
1 p.
article
                             19 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands