| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel mitochondrial tRNALeu(UUR) mutation in a patient with features of MERRF and Kearns–Sayre syndrome
|
Nishigaki, Yutaka
|
|
2003
|
13 |
4 |
p. 334-340
7 p.
|
artikel
|
| 2 |
Assessment of cardiovascular autonomic function in myotonic dystrophy type 2 (DM2/PROMM)
|
Flachenecker, Peter
|
|
2003
|
13 |
4 |
p. 289-293
5 p.
|
artikel
|
| 3 |
Cardiomyopathic features associated with muscular dystrophy are independent of dystrophin absence in cardiovasculature
|
Hainsey, T.A.
|
|
2003
|
13 |
4 |
p. 294-302
9 p.
|
artikel
|
| 4 |
Channelopathies – common mechanisms in aura, arrhythmia and alkalosis, Edited by F. Lehmann-Horn and K. Jurkat-Rott, Elsevier, 368 pages, ISBN: 0-444-50489-3, Euro 179
|
Hanna, Michael G.
|
|
2003
|
13 |
4 |
p. 353-
1 p.
|
artikel
|
| 5 |
Channelopathies of the Nervous System
|
Davies, Nick
|
|
2003
|
13 |
4 |
p. 352-
1 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2003
|
13 |
4 |
p. CO2-
1 p.
|
artikel
|
| 7 |
Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress
|
Winokur, Sara T
|
|
2003
|
13 |
4 |
p. 322-333
12 p.
|
artikel
|
| 8 |
Instructions to Authors
|
|
|
2003
|
13 |
4 |
p. 354-355
2 p.
|
artikel
|
| 9 |
LGMD2E patients risk developing dilated cardiomyopathy
|
Fanin, M.
|
|
2003
|
13 |
4 |
p. 303-309
7 p.
|
artikel
|
| 10 |
MYOTONIC DYSTROPHY ‘the facts’ by Peter S. Harper, Printed by OUP. Price £10.99, ISBN 0 19 852586-9
|
Bowler, M.A.
|
|
2003
|
13 |
4 |
p. 352-
1 p.
|
artikel
|
| 11 |
102nd ENMC International Workshop on Schwartz–Jampel Syndrome, 14–16 December, 2001, Naarden, The Netherlands
|
Nicole, Sophie
|
|
2003
|
13 |
4 |
p. 347-351
5 p.
|
artikel
|
| 12 |
Pathological characteristics of skeletal muscle in Ullrich's disease with collagen VI deficiency
|
Higuchi, Itsuro
|
|
2003
|
13 |
4 |
p. 310-316
7 p.
|
artikel
|
| 13 |
Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contractures
|
Helderman-van den Enden, A.T.J.M.
|
|
2003
|
13 |
4 |
p. 317-321
5 p.
|
artikel
|
| 14 |
Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene
|
Azzedine, H
|
|
2003
|
13 |
4 |
p. 341-346
6 p.
|
artikel
|
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