| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A family with autosomal dominant mutilating neuropathy not linked to either Charcot–Marie–Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci
|
Bellone, Emilia
|
|
2002
|
12 |
3 |
p. 286-291
6 p.
|
artikel
|
| 2 |
A quantitative study of bioenergetics in skeletal muscle lacking utrophin and dystrophin
|
Cole, M.A.
|
|
2002
|
12 |
3 |
p. 247-257
11 p.
|
artikel
|
| 3 |
Bethlem myopathy (BETHLEM) 86th ENMC International Workshop, 10–11 November 2000, Naarden, The Netherlands
|
Pepe, Guglielmina
|
|
2002
|
12 |
3 |
p. 296-305
10 p.
|
artikel
|
| 4 |
Charles Bell (1774–1842) and an early case of muscular dystrophy
|
Gardner-Thorpe, Christopher
|
|
2002
|
12 |
3 |
p. 318-321
4 p.
|
artikel
|
| 5 |
Defects of mitochondrial β-oxidation: a growing group of disorders
|
Vockley, Jerry
|
|
2002
|
12 |
3 |
p. 235-246
12 p.
|
artikel
|
| 6 |
Instructions to authors
|
|
|
2002
|
12 |
3 |
p. 340-341
2 p.
|
artikel
|
| 7 |
Involvement of KCa2+ channels in the local abnormalities and hyperkalemia following the ischemia-reperfusion injury of rat skeletal muscle
|
Tricarico, Domenico
|
|
2002
|
12 |
3 |
p. 258-265
8 p.
|
artikel
|
| 8 |
Letter on Schneider article
|
Mahjneh, Ibrahim
|
|
2002
|
12 |
3 |
p. 322-
1 p.
|
artikel
|
| 9 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
2002
|
12 |
3 |
p. 334-339
6 p.
|
artikel
|
| 10 |
Neuromuscular disorders: gene location
|
|
|
2002
|
12 |
3 |
p. 324-333
10 p.
|
artikel
|
| 11 |
Normal calcium homeostasis in dystrophin-expressing facioscapulohumeral muscular dystrophy myotubes
|
Vandebrouck, Clarisse
|
|
2002
|
12 |
3 |
p. 266-272
7 p.
|
artikel
|
| 12 |
Presynaptic neuromuscular transmission block in Guillain–Barré syndrome associated with anti-GQ1b antibodies
|
Wirguin, I.
|
|
2002
|
12 |
3 |
p. 292-293
2 p.
|
artikel
|
| 13 |
Primary γ-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile
|
Bönnemann, C.G.
|
|
2002
|
12 |
3 |
p. 273-280
8 p.
|
artikel
|
| 14 |
Report of the 84th ENMC Workshop: PROMM (Proximal Myotonic Myopathy) and Other Myotonic Dystrophy-Like Syndromes: 2nd Workshop. 13–15th October, 2000, Loosdrecht, The Netherlands
|
Moxley III, Richard T.
|
|
2002
|
12 |
3 |
p. 306-317
12 p.
|
artikel
|
| 15 |
Response from author
|
Schneider, C.
|
|
2002
|
12 |
3 |
p. 322-323
2 p.
|
artikel
|
| 16 |
The gene for a novel glycosyltransferase is mutated in congenital muscular dystrophy MDC1C and limb girdle muscular dystrophy 2I
|
Brockington, Martin
|
|
2002
|
12 |
3 |
p. 233-234
2 p.
|
artikel
|
| 17 |
Two amino-acid substitutions in the myelin protein zero gene of a case of Charcot–Marie–Tooth disease associated with light-near dissociation
|
Bienfait, H.M.E.
|
|
2002
|
12 |
3 |
p. 281-285
5 p.
|
artikel
|
| 18 |
Vertebral compression in Duchenne muscular dystrophy following deflazacort
|
Talim, B.
|
|
2002
|
12 |
3 |
p. 294-295
2 p.
|
artikel
|
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