| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Arthrogryposis multiplex in a newborn of a myasthenic mother—Case report and literature
|
Dinger, J.
|
|
1993
|
3 |
4 |
p. 335-339
5 p.
|
artikel
|
| 2 |
Brown-Séquard: A visionary of science
|
Emery, Alan
|
|
1993
|
3 |
4 |
p. 349-350
2 p.
|
artikel
|
| 3 |
Degradative activity of granzyme A on skeletal muscle proteins in vitro: A possible molecular mechanism for muscle fiber damage in polymyositis
|
Nakamura, Koichiro
|
|
1993
|
3 |
4 |
p. 303-310
8 p.
|
artikel
|
| 4 |
Development of electrical myotonia in the ADR mouse: Role of chloride conductance in myotubes and neonatal animals
|
Wischmeyer, Erhard
|
|
1993
|
3 |
4 |
p. 267-274
8 p.
|
artikel
|
| 5 |
Duchenne muscular dystrophy—Meryon's disease
|
Emery, Alan E.H.
|
|
1993
|
3 |
4 |
p. 263-266
4 p.
|
artikel
|
| 6 |
Evaluation of electrophysiological and clinical tests in an exploratory trial of Org 2766 in motor neuron disease
|
Hesselmans, L.F.G.M.
|
|
1993
|
3 |
4 |
p. 319-325
7 p.
|
artikel
|
| 7 |
Guillain-Barré syndrome
|
Gordon, Neil
|
|
1993
|
3 |
4 |
p. 349-
1 p.
|
artikel
|
| 8 |
Linkage and apparent heterogeneity in proximal spinal muscular atrophies
|
Cobben, Jan M.
|
|
1993
|
3 |
4 |
p. 327-333
7 p.
|
artikel
|
| 9 |
Meryon's disease
|
Dubowitz, V.
|
|
1993
|
3 |
4 |
p. 261-
1 p.
|
artikel
|
| 10 |
Molecular and cellular approaches to the treatment of neurological disease
|
Read, Andrew P.
|
|
1993
|
3 |
4 |
p. 347-
1 p.
|
artikel
|
| 11 |
Molecular basis of neurology
|
Emery, Alan
|
|
1993
|
3 |
4 |
p. 347-348
2 p.
|
artikel
|
| 12 |
Monomelic muscle atrophy
|
Takemitsu, Masakazu
|
|
1993
|
3 |
4 |
p. 311-317
7 p.
|
artikel
|
| 13 |
Myopathy of the Proteus syndrome: Hypothesis of muscular dysgenesis
|
Sarnat, Harvey B.
|
|
1993
|
3 |
4 |
p. 293-301
9 p.
|
artikel
|
| 14 |
Neuromuscular disorders: Gene location
|
|
|
1993
|
3 |
4 |
p. 341-346
6 p.
|
artikel
|
| 15 |
Retrovirus-mediated gene transfer of transthyretin and transthyretin-methionine 30: A potential tool for the study of amyloidogenesis
|
Bonifácio, Maria João
|
|
1993
|
3 |
4 |
p. 275-282
8 p.
|
artikel
|
| 16 |
The genetic basis of common diseases
|
Mueller, R.F.
|
|
1993
|
3 |
4 |
p. 348-349
2 p.
|
artikel
|
| 17 |
Ubiquitin and β-amyloid-protein in inclusion body myositis (IBM), familial IBM-like disorder and oculopharyngeal muscular dystrophy: An immunocytochemical study
|
Leclerc, Anne
|
|
1993
|
3 |
4 |
p. 283-291
9 p.
|
artikel
|
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