| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritance
|
Manzur, A.Y
|
|
1998
|
8 |
7 |
p. 467-473
7 p.
|
artikel
|
| 2 |
Autosomal dominant late adult onset distal leg myopathy
|
Pénisson-Besnier, Isabelle
|
|
1998
|
8 |
7 |
p. 459-466
8 p.
|
artikel
|
| 3 |
Autosomal recessive spastic ataxia of Charlevoix–Saguenay
|
Bouchard, Jean-Pierre
|
|
1998
|
8 |
7 |
p. 474-479
6 p.
|
artikel
|
| 4 |
Book review
|
|
|
1998
|
8 |
7 |
p. 528-
1 p.
|
artikel
|
| 5 |
Book review
|
|
|
1998
|
8 |
7 |
p. 526-
1 p.
|
artikel
|
| 6 |
Book review
|
|
|
1998
|
8 |
7 |
p. 529-530
2 p.
|
artikel
|
| 7 |
Book review
|
|
|
1998
|
8 |
7 |
p. 530-531
2 p.
|
artikel
|
| 8 |
Book review
|
|
|
1998
|
8 |
7 |
p. 528-529
2 p.
|
artikel
|
| 9 |
Book review
|
|
|
1998
|
8 |
7 |
p. 527-528
2 p.
|
artikel
|
| 10 |
Book review
|
|
|
1998
|
8 |
7 |
p. 529-
1 p.
|
artikel
|
| 11 |
Book review
|
|
|
1998
|
8 |
7 |
p. 526-527
2 p.
|
artikel
|
| 12 |
Book review
|
|
|
1998
|
8 |
7 |
p. 527-
1 p.
|
artikel
|
| 13 |
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization
|
Rosenberg, C.
|
|
1998
|
8 |
7 |
p. 447-452
6 p.
|
artikel
|
| 14 |
Dystrophinopathy in a boy with Chediak–Higashi syndrome
|
von Moers, Arpad
|
|
1998
|
8 |
7 |
p. 489-494
6 p.
|
artikel
|
| 15 |
Impaired aerobic glycolysis in muscle phosphofructokinase deficiency results in biphasic post-exercise phosphocreatine recovery in 31P magnetic resonance spectroscopy
|
Grehl, T
|
|
1998
|
8 |
7 |
p. 480-488
9 p.
|
artikel
|
| 16 |
Laminin α2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy
|
Naom, I
|
|
1998
|
8 |
7 |
p. 495-501
7 p.
|
artikel
|
| 17 |
MTM1 gene mutations in Japanese patients with the severe infantile form of myotubular myopathy
|
Nishino, Ichizo
|
|
1998
|
8 |
7 |
p. 453-458
6 p.
|
artikel
|
| 18 |
Presence of emerinopathy in cases of rigid spine syndrome
|
Kubo, Shinichiro
|
|
1998
|
8 |
7 |
p. 502-507
6 p.
|
artikel
|
| 19 |
PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafness
|
Phillips, M.F
|
|
1998
|
8 |
7 |
p. 439-446
8 p.
|
artikel
|
| 20 |
Proximal myotonic myopathy (PROMM) and other proximal myotonic syndromes
|
Moxley III, Richard T
|
|
1998
|
8 |
7 |
p. 519-520
2 p.
|
artikel
|
| 21 |
54th ENMC International Workshop: PROMM (Proximal Myotonic Myopathies) and Other Proximal Myotonic Syndromes 10–12th October 1997, Naarden, The Netherlands
|
Moxley, Richard T
|
|
1998
|
8 |
7 |
p. 508-518
11 p.
|
artikel
|
| 22 |
58th ENMC Workshop: Myotubular Myopathy, 20–22 March, 1998, Naarden, The Netherlands
|
Wallgren-Pettersson, Carina
|
|
1998
|
8 |
7 |
p. 521-525
5 p.
|
artikel
|
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