| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adult glycogenosis II with paracrystalline mitochondrial inclusions and Hirano bodies in skeletal muscle
|
Fernández, Roberto
|
|
1999
|
9 |
3 |
p. 136-143
8 p.
|
artikel
|
| 2 |
A new mutation in the myophosphorylase gene (Asn684Tyr) in a Spanish patient with McArdle's disease
|
Andreu, Antonio L
|
|
1999
|
9 |
3 |
p. 171-173
3 p.
|
artikel
|
| 3 |
Book review
|
|
|
1999
|
9 |
3 |
p. 200-201
2 p.
|
artikel
|
| 4 |
Book review
|
|
|
1999
|
9 |
3 |
p. 200-
1 p.
|
artikel
|
| 5 |
Congenital myasthenic syndrome caused by a mutation in the Ets-binding site of the promoter region of the acetylcholine receptor ϵ subunit gene
|
Ohno, K
|
|
1999
|
9 |
3 |
p. 131-135
5 p.
|
artikel
|
| 6 |
Correlation of muscle fiber type measurements with clinical and molecular genetic data in Duchenne muscular dystrophy
|
Wang, Jian-Feng
|
|
1999
|
9 |
3 |
p. 150-158
9 p.
|
artikel
|
| 7 |
Effect of mexiletine on sea anemone toxin-induced non-inactivating sodium channels of rat skeletal muscle: a model of sodium channel myotonia
|
Desaphy, J.-F
|
|
1999
|
9 |
3 |
p. 182-189
8 p.
|
artikel
|
| 8 |
Familial infantile myasthenia: confusion in terminology
|
Deymeer, F
|
|
1999
|
9 |
3 |
p. 129-130
2 p.
|
artikel
|
| 9 |
Genotype-phenotype analysis in X-linked Emery–Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype
|
Yates, John R.W
|
|
1999
|
9 |
3 |
p. 159-165
7 p.
|
artikel
|
| 10 |
Lower limb surgery in Duchenne muscular dystrophy
|
Forst, J
|
|
1999
|
9 |
3 |
p. 176-181
6 p.
|
artikel
|
| 11 |
McArdle's disease associated with homozygosity for the missense mutation Gly204Ser of the myophosphorylase gene in a Spanish patient
|
Rubio, Juan C
|
|
1999
|
9 |
3 |
p. 174-175
2 p.
|
artikel
|
| 12 |
Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease
|
Galluzzi, G
|
|
1999
|
9 |
3 |
p. 190-198
9 p.
|
artikel
|
| 13 |
Proximal myotonic myopathy (PROMM) presenting as myotonia during pregnancy
|
Newman, B
|
|
1999
|
9 |
3 |
p. 144-149
6 p.
|
artikel
|
| 14 |
Severe clinical expression in X-linked Emery–Dreifuss muscular dystrophy
|
Hoeltzenbein, Maria
|
|
1999
|
9 |
3 |
p. 166-170
5 p.
|
artikel
|
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