| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21
|
Xiang, Fengqing
|
|
1999
|
9 |
5 |
p. 308-312
5 p.
|
artikel
|
| 2 |
Behavioral characterization of mdx3cv mice deficient in C-terminal dystrophins
|
Vaillend, Cyrille
|
|
1999
|
9 |
5 |
p. 296-304
9 p.
|
artikel
|
| 3 |
Book review
|
|
|
1999
|
9 |
5 |
p. 356-357
2 p.
|
artikel
|
| 4 |
Book review
|
|
|
1999
|
9 |
5 |
p. 358-
1 p.
|
artikel
|
| 5 |
Book review
|
|
|
1999
|
9 |
5 |
p. 355-
1 p.
|
artikel
|
| 6 |
Book review
|
|
|
1999
|
9 |
5 |
p. 357-358
2 p.
|
artikel
|
| 7 |
Book review
|
|
|
1999
|
9 |
5 |
p. 355-356
2 p.
|
artikel
|
| 8 |
Book review
|
|
|
1999
|
9 |
5 |
p. 356-
1 p.
|
artikel
|
| 9 |
Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy
|
Hoogerwaard, E.M.
|
|
1999
|
9 |
5 |
p. 347-351
5 p.
|
artikel
|
| 10 |
Cognitive and psychological profile of a Tunisian population of limb girdle muscular dystrophy
|
Miladi, Najoua
|
|
1999
|
9 |
5 |
p. 352-354
3 p.
|
artikel
|
| 11 |
Decreased expression of laminin β1 in chromosome 21-linked Bethlem myopathy
|
Merlini, L
|
|
1999
|
9 |
5 |
p. 326-329
4 p.
|
artikel
|
| 12 |
Infantile lipid storage myopathy with nocturnal hypoventilation shows abnormal low-affinity muscle carnitine uptake in vitro
|
Vergani, Lodovica
|
|
1999
|
9 |
5 |
p. 320-322
3 p.
|
artikel
|
| 13 |
Mitochondrial 3243 A→G mutation (MELAS mutation) associated with painful muscle stiffness
|
Deschauer, M.
|
|
1999
|
9 |
5 |
p. 305-307
3 p.
|
artikel
|
| 14 |
Molecular analysis of a spontaneous dystrophin `knockout' dog
|
Schatzberg, Scott J
|
|
1999
|
9 |
5 |
p. 289-295
7 p.
|
artikel
|
| 15 |
Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype
|
Scholte, H.R.
|
|
1999
|
9 |
5 |
p. 313-319
7 p.
|
artikel
|
| 16 |
Prenatal diagnosis in a family affected with β-sarcoglycan muscular dystrophy
|
Pegoraro, Elena
|
|
1999
|
9 |
5 |
p. 323-325
3 p.
|
artikel
|
| 17 |
Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides
|
Wilton, Stephen D
|
|
1999
|
9 |
5 |
p. 330-338
9 p.
|
artikel
|
| 18 |
X-linked dilated cardiomyopathy and the dystrophin gene
|
Ferlini, Alessandra
|
|
1999
|
9 |
5 |
p. 339-346
8 p.
|
artikel
|
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