| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A curious experiment: the paradigm switch from observation and speculation to experimentation, in the understanding of neuromuscular function and disease
|
Pearn, John
|
|
2002
|
12 |
6 |
p. 600-607
8 p.
|
article
|
| 2 |
A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population
|
Gross, M
|
|
2002
|
12 |
6 |
p. 558-565
8 p.
|
article
|
| 3 |
An expanding view for the molecular basis of familial periodic paralysis
|
Cannon, Stephen C
|
|
2002
|
12 |
6 |
p. 533-543
11 p.
|
article
|
| 4 |
Comment on Connolly AM, et al. Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin α2-deficient mice (Neuromuscul Disord 2001;11:703–712)
|
Vrbová, Gerta
|
|
2002
|
12 |
6 |
p. 608-609
2 p.
|
article
|
| 5 |
Congenital myasthenic syndrome associated with episodic apnea and sudden infant death
|
Byring, R.F
|
|
2002
|
12 |
6 |
p. 548-553
6 p.
|
article
|
| 6 |
Diaphragm kinetics during pneumatic belt respiratory assistance: a sonographic study in Duchenne muscular dystrophy
|
Ayoub, Jean
|
|
2002
|
12 |
6 |
p. 569-575
7 p.
|
article
|
| 7 |
Dose-dependent effect of individualized respiratory muscle training in children with Duchenne muscular dystrophy
|
Topin, Nathalie
|
|
2002
|
12 |
6 |
p. 576-583
8 p.
|
article
|
| 8 |
Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?
|
Tonini, M.M.O
|
|
2002
|
12 |
6 |
p. 554-557
4 p.
|
article
|
| 9 |
Instructions to authors
|
|
|
2002
|
12 |
6 |
p. 610-611
2 p.
|
article
|
| 10 |
Multifocal motor neuropathy and asymptomatic Hashimoto's thyroiditis: first report of an association
|
Toscano, Antonio
|
|
2002
|
12 |
6 |
p. 566-568
3 p.
|
article
|
| 11 |
Publisher’s note
|
|
|
2002
|
12 |
6 |
p. iii-
1 p.
|
article
|
| 12 |
Response to comments by G. Vrbová
|
Connolly, Anne M
|
|
2002
|
12 |
6 |
p. 609-
1 p.
|
article
|
| 13 |
99th ENMC international workshop: myotonic dystrophy: present management, future therapy
|
Harper, P.S
|
|
2002
|
12 |
6 |
p. 596-599
4 p.
|
article
|
| 14 |
Transected myofibres may remain permanently divided in two parts
|
Vaittinen, Samuli
|
|
2002
|
12 |
6 |
p. 584-587
4 p.
|
article
|
| 15 |
Welander distal myopathy outside the Swedish population: phenotype and genotype
|
von Tell, Désirée
|
|
2002
|
12 |
6 |
p. 544-547
4 p.
|
article
|
| 16 |
Workshop report of the 89th ENMC International Workshop: Central Core Disease, 19th–20th January 2001, Hilversum, The Netherlands
|
De Cauwer, Harald
|
|
2002
|
12 |
6 |
p. 588-595
8 p.
|
article
|
Journal description