nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Abnormal oxidative metabolism in exercise in exercise intolerance of undetermined origin
|
Argov, Z. |
|
1997 |
7 |
2 |
p. 99-104 6 p. |
artikel |
2 |
A double blind cross over trial of theophylline prophylaxis for sleep hypoxaemia in Duchenne muscular dystrophy
|
Khan, Y. |
|
1997 |
7 |
2 |
p. 75-80 6 p. |
artikel |
3 |
Announcements
|
|
|
1997 |
7 |
2 |
p. 138- 1 p. |
artikel |
4 |
A novel SOD1 mutation in an Austrian family with amyotrophic lateral sclerosis
|
Bereznai, Benjamin |
|
1997 |
7 |
2 |
p. 113-116 4 p. |
artikel |
5 |
Clinical disorders of balance posture and gait
|
Venables, Graham |
|
1997 |
7 |
2 |
p. 140- 1 p. |
artikel |
6 |
Clinical neurophysiology
|
Cull, Roger E. |
|
1997 |
7 |
2 |
p. 139- 1 p. |
artikel |
7 |
Clinical skills in neurology
|
Mumford, Colin J. |
|
1997 |
7 |
2 |
p. 139-140 2 p. |
artikel |
8 |
Impaired functional and structural recovery after muscle injury in dystrophic mdx mice
|
Irintchev, A. |
|
1997 |
7 |
2 |
p. 117-125 9 p. |
artikel |
9 |
Inaugural meeting of the Meryon Society
|
Emery, Alan E.H. |
|
1997 |
7 |
2 |
p. 133- 1 p. |
artikel |
10 |
Intracellular detection of laminin α 2 chain in skin by electron microscopy immunocytochemistry: Comparison between normal and laminin α 2 chain deficient subjects
|
Squarzoni, S. |
|
1997 |
7 |
2 |
p. 91-98 8 p. |
artikel |
11 |
Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency
|
Tan, Ersin |
|
1997 |
7 |
2 |
p. 85-89 5 p. |
artikel |
12 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
1997 |
7 |
2 |
p. XIII-XVIII nvt p. |
artikel |
13 |
Neuromuscular disorders: gene location
|
|
|
1997 |
7 |
2 |
p. I-XI nvt p. |
artikel |
14 |
Paramyotonia congenita and hyperkalemic periodic paralysis associated with a Met 1592 Val substitution in the skeletal muscle sodium channel α subunit — a large kindred with a novel phenotype
|
Kelly, P. |
|
1997 |
7 |
2 |
p. 105-111 7 p. |
artikel |
15 |
Paramyotonia, potassium-aggravated myotonias and periodic paralyses. 37th ENMC International Workshop, Naarden, The Netherlands, 8 – 10 December 1995
|
|
|
1997 |
7 |
2 |
p. 127-132 6 p. |
artikel |
16 |
Stroke therapy
|
Davenport, Richard |
|
1997 |
7 |
2 |
p. 140- 1 p. |
artikel |
17 |
Sudden infant death syndrome (SIDS) in a family with myosphosphorylase deficiency
|
El-Schahawi, M. |
|
1997 |
7 |
2 |
p. 81-83 3 p. |
artikel |
18 |
The European Neuromuscular Centre (ENMC): importance of collaborative research
|
Emery, Alan E.H. |
|
1997 |
7 |
2 |
p. 135-137 3 p. |
artikel |
19 |
Wilson's disease (major problems in neurology 30)
|
Quinn, Niall |
|
1997 |
7 |
2 |
p. 141- 1 p. |
artikel |