| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies
|
Richard, Isabelle
|
|
1999
|
9 |
8 |
p. 555-563
9 p.
|
article
|
| 2 |
Adult onset reducing body myopathy
|
Figarella-Branger, D
|
|
1999
|
9 |
8 |
p. 580-586
7 p.
|
article
|
| 3 |
Association of monoamine oxidase B alleles with age at onset in amyotrophic lateral sclerosis
|
Orrù, S.
|
|
1999
|
9 |
8 |
p. 593-597
5 p.
|
article
|
| 4 |
Cardiac involvement in Becker's muscular dystrophy, necessitating heart transplantation, 6 years before apparent skeletal muscle involvement
|
Finsterer, J
|
|
1999
|
9 |
8 |
p. 598-600
3 p.
|
article
|
| 5 |
Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy
|
Wallgren-Pettersson, Carina
|
|
1999
|
9 |
8 |
p. 564-572
9 p.
|
article
|
| 6 |
Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies
|
Herczegfalvi, Á
|
|
1999
|
9 |
8 |
p. 552-554
3 p.
|
article
|
| 7 |
Expression, regulation and localisation of dystrophin isoforms in human foetal skeletal and cardiac muscle
|
Torelli, Silvia
|
|
1999
|
9 |
8 |
p. 541-551
11 p.
|
article
|
| 8 |
Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy
|
Tan, P.
|
|
1999
|
9 |
8 |
p. 573-579
7 p.
|
article
|
| 9 |
Immunosuppressive treatment of rippling muscles in patients with myasthenia gravis
|
Müller-Felber, W
|
|
1999
|
9 |
8 |
p. 604-607
4 p.
|
article
|
| 10 |
Index
|
|
|
1999
|
9 |
8 |
p. xx-xxiii
nvt p.
|
article
|
| 11 |
Index
|
|
|
1999
|
9 |
8 |
p. xxiv-xxvi
nvt p.
|
article
|
| 12 |
Multiple paraneoplastic diseases associated with thymoma
|
Evoli, A
|
|
1999
|
9 |
8 |
p. 601-603
3 p.
|
article
|
| 13 |
Novel chloride channel gene mutations in two unrelated Japanese families with Becker's autosomal recessive generalized myotonia
|
Sasaki, Ryogen
|
|
1999
|
9 |
8 |
p. 587-592
6 p.
|
article
|
Journal description