| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A modified alignment of human and rodent 5′ untranslated sequences of the acetylcholine receptor epsilon subunit gene reveals additional regions of high homology
|
Stucka, Rolf
|
|
2000
|
10 |
3 |
p. 213-
1 p.
|
artikel
|
| 2 |
An inherited 4q35- Eco RI-DNA-fragment of 35 kb in a family with a sporadic case of facioscapulohumeral muscular dystrophy (FSHD)
|
Busse, K.
|
|
2000
|
10 |
3 |
p. 178-181
4 p.
|
artikel
|
| 3 |
Antimyotonic effects of tocainide enantiomers on skeletal muscle fibers of congenitally myotonic goats
|
Camerino, Diana Conte
|
|
2000
|
10 |
3 |
p. 160-164
5 p.
|
artikel
|
| 4 |
Book review
|
Emery, Alan E.H
|
|
2000
|
10 |
3 |
p. 216-
1 p.
|
artikel
|
| 5 |
Book reviews
|
Lodi, Raffaele
|
|
2000
|
10 |
3 |
p. 215-
1 p.
|
artikel
|
| 6 |
Expression and synthesis of alternatively spliced variants of Dp71 in adult human brain
|
Austin, Richard C.
|
|
2000
|
10 |
3 |
p. 187-193
7 p.
|
artikel
|
| 7 |
Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patient
|
Thuillier, L.
|
|
2000
|
10 |
3 |
p. 200-205
6 p.
|
artikel
|
| 8 |
Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies
|
Dubourg, Odile
|
|
2000
|
10 |
3 |
p. 206-208
3 p.
|
artikel
|
| 9 |
Historical Studies in Neuromuscular Disorders
|
Emery, A.E.H
|
|
2000
|
10 |
3 |
p. 211-212
2 p.
|
artikel
|
| 10 |
Hypothyroidism unmasking proximal myotonic myopathy
|
Sansone, V.
|
|
2000
|
10 |
3 |
p. 165-172
8 p.
|
artikel
|
| 11 |
Letter to the Editor
|
Ohno, Kinji
|
|
2000
|
10 |
3 |
p. 214-
1 p.
|
artikel
|
| 12 |
Lipopolysaccharides of a Campylobacter coli isolate from a patient with Guillain–Barré syndrome display ganglioside mimicry
|
Bersudsky, Marina
|
|
2000
|
10 |
3 |
p. 182-186
5 p.
|
artikel
|
| 13 |
Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies
|
Bardoni, Alessandra
|
|
2000
|
10 |
3 |
p. 194-199
6 p.
|
artikel
|
| 14 |
Oculopharyngeal muscular dystrophy in a Japanese family with a short GCG expansion (GCG)11 in PABP2 gene
|
Nagashima, Toshiko
|
|
2000
|
10 |
3 |
p. 173-177
5 p.
|
artikel
|
| 15 |
The Fukuyama congenital muscular dystrophy story
|
Toda, Tatsushi
|
|
2000
|
10 |
3 |
p. 153-159
7 p.
|
artikel
|
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