| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A discrepancy resolved: human satellite cells are not preprogrammed to fast and slow lineages
|
Bonavaud, Sylvie
|
|
2001
|
11 |
8 |
p. 747-752
6 p.
|
artikel
|
| 2 |
Author Index
|
|
|
2001
|
11 |
8 |
p. VII-XI
nvt p.
|
artikel
|
| 3 |
Axon damage in CMT due to mutation in myelin protein P0
|
Hanemann, C.O
|
|
2001
|
11 |
8 |
p. 753-756
4 p.
|
artikel
|
| 4 |
Central Nervous System AngiitisJames W. Schmidley, April 2000, 240 pages, hardback, Heinemann Publishers, Oxford. ISBN: 0 7506 7153, £70.00
|
Bousser, Marie-Germaine
|
|
2001
|
11 |
8 |
p. 761-
1 p.
|
artikel
|
| 5 |
Charcot: Constructing Neurology Goetz CG, Bonduelle M, Gelfand T. Oxford University Press, New York, Oxford, 1995. ISBN 0-19-507643-5 (Cloth), 392 pp. Price £45.00
|
Emery, Alan E.H.
|
|
2001
|
11 |
8 |
p. 762-
1 p.
|
artikel
|
| 6 |
Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblasts
|
Furling, Denis
|
|
2001
|
11 |
8 |
p. 728-735
8 p.
|
artikel
|
| 7 |
Handbook of Ataxia Disorders Klockgether T, August 2000, 712 pp Marcel Dekker Inc. New York, ISBN: 0 8247 03812 $215
|
Hanna, Michael G.
|
|
2001
|
11 |
8 |
p. 762-763
2 p.
|
artikel
|
| 8 |
Handbook of Sleep MedicineJ. Shneerson, March 2000, 256 pages, 56 illustrations, hardback, Blackwell Science, Oxford. ISBN: 0 632 05135 3, £49.50
|
|
|
2001
|
11 |
8 |
p. 760-
1 p.
|
artikel
|
| 9 |
Instructions to authors
|
|
|
2001
|
11 |
8 |
p. 780-781
2 p.
|
artikel
|
| 10 |
Introduction to Clinical Neurology, 2nd editionDouglas J. Gelb, May 2000, 416 pages, Butterworth Heinemann: London. ISBN 0750672021, £22.50
|
Nichols, Philip
|
|
2001
|
11 |
8 |
p. 760-761
2 p.
|
artikel
|
| 11 |
Keyword Index
|
|
|
2001
|
11 |
8 |
p. XII-XIV
nvt p.
|
artikel
|
| 12 |
Management Of Persons With Chronic Neurologic Illness Ozer, Mark.352 pp, 254×178 mm: 15 line illustrations: Butterworth, Heinemann, Hardcover: March 2000 £45 ISBN 0 7506 7005 3
|
Collin, Christine
|
|
2001
|
11 |
8 |
p. 762-
1 p.
|
artikel
|
| 13 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
2001
|
11 |
8 |
p. 774-779
6 p.
|
artikel
|
| 14 |
Neuromuscular disorders: gene location
|
|
|
2001
|
11 |
8 |
p. 764-773
10 p.
|
artikel
|
| 15 |
Non-toxic ubiquitous over-expression of utrophin in the mdx mouse
|
Fisher, Rosie
|
|
2001
|
11 |
8 |
p. 713-721
9 p.
|
artikel
|
| 16 |
Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture system
|
Dorchies, Olivier M
|
|
2001
|
11 |
8 |
p. 736-746
11 p.
|
artikel
|
| 17 |
Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy
|
Minami, Narihiro
|
|
2001
|
11 |
8 |
p. 699-702
4 p.
|
artikel
|
| 18 |
Selective changes in mitochondria respiratory properties in oxidative or glycolytic muscle fibers isolated from G93AhumanSOD1 transgenic mice
|
Leclerc, Nathalie
|
|
2001
|
11 |
8 |
p. 722-727
6 p.
|
artikel
|
| 19 |
Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin α2-deficient mice
|
Connolly, Anne M
|
|
2001
|
11 |
8 |
p. 703-712
10 p.
|
artikel
|
| 20 |
Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiency
|
Kottlors, Michael
|
|
2001
|
11 |
8 |
p. 757-759
3 p.
|
artikel
|
| 21 |
Volume contents
|
|
|
2001
|
11 |
8 |
p. I-VI
nvt p.
|
artikel
|
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