| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies
|
Meola, Giovanni
|
|
1996
|
6 |
3 |
p. 143-150
8 p.
|
artikel
|
| 2 |
An introduction to recombinant DNA in medicine, second edition
|
Porteous, Mary
|
|
1996
|
6 |
3 |
p. 222-
1 p.
|
artikel
|
| 3 |
Application of in vitro myo-differentiation of non-muscle cells to enhance gene expression and facilitate analysis of muscle proteins
|
Roest, P.A.M.
|
|
1996
|
6 |
3 |
p. 195-202
8 p.
|
artikel
|
| 4 |
Bailliere's clinical neurology: Cerebrovascular disease
|
Venables, Graham
|
|
1996
|
6 |
3 |
p. 224-
1 p.
|
artikel
|
| 5 |
Clinical heterogeneity of seronegative myasthenia gravis
|
Evoli, A.
|
|
1996
|
6 |
3 |
p. 155-161
7 p.
|
artikel
|
| 6 |
Digital EEG in clinical practice
|
Cull, Roger E.
|
|
1996
|
6 |
3 |
p. 225-
1 p.
|
artikel
|
| 7 |
HTLV-1 polymyositis
|
Caldwell, C.J.
|
|
1996
|
6 |
3 |
p. 151-154
4 p.
|
artikel
|
| 8 |
Metabolic myopathies
|
Mitchell, J.D.
|
|
1996
|
6 |
3 |
p. 222-223
2 p.
|
artikel
|
| 9 |
Mitochondrial abnormalities in oculopharyngeal muscular dystrophy
|
Wong, Kum Thong
|
|
1996
|
6 |
3 |
p. 163-166
4 p.
|
artikel
|
| 10 |
Mitochondrial encephalomyopathies: Gene mutation
|
|
|
1996
|
6 |
3 |
p. XI-XIV
nvt p.
|
artikel
|
| 11 |
Muscle disorders in childhood, second edition
|
Brown, J.K.
|
|
1996
|
6 |
3 |
p. 224-
1 p.
|
artikel
|
| 12 |
Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiency
|
Villanova, M.
|
|
1996
|
6 |
3 |
p. 167-172
6 p.
|
artikel
|
| 13 |
Negative motor phenomena (Advances in neurology, volume 67)
|
Duncan, Roderick
|
|
1996
|
6 |
3 |
p. 221-
1 p.
|
artikel
|
| 14 |
Nerve terminal sprouting in botulinum type-A treated mouse levator auris longus muscle
|
Juzans, Pascal
|
|
1996
|
6 |
3 |
p. 177-185
9 p.
|
artikel
|
| 15 |
Neuromuscular disorders: Gene location
|
|
|
1996
|
6 |
3 |
p. I-IX
nvt p.
|
artikel
|
| 16 |
Parkinson's disease — A guide for patient and family, fourth edition
|
Smith, Roger G.
|
|
1996
|
6 |
3 |
p. 223-
1 p.
|
artikel
|
| 17 |
Pathogenesis and therapy of amyotrophic lateral sclerosis (Advances in neurology, volume 68)
|
Mitchell, J.D.
|
|
1996
|
6 |
3 |
p. 225-226
2 p.
|
artikel
|
| 18 |
Prenatal diagnosis of limb-girdle muscular dystrophy type 2A
|
Restagno, G.
|
|
1996
|
6 |
3 |
p. 173-176
4 p.
|
artikel
|
| 19 |
Reduction of serum IgG level and peripheral T-cell counts are correlated with CTG repeat lengths in myotonic dystrophy patients
|
Nakamura, Akinori
|
|
1996
|
6 |
3 |
p. 203-210
8 p.
|
artikel
|
| 20 |
Research database for dystrophin gene and protein expression 35th ENMC Workshop, 6–8 October 1995, Naarden, The Netherlands
|
Anderson, L.V.B.
|
|
1996
|
6 |
3 |
p. 219-
1 p.
|
artikel
|
| 21 |
Role of nicotinic acetylcholine receptors at the vertebrate myotendinous junction: a hypothesis
|
Bernheim, L.
|
|
1996
|
6 |
3 |
p. 211-214
4 p.
|
artikel
|
| 22 |
Successive injections in MDX mice of myoblasts grown with bFGF
|
Kinoshita, I.
|
|
1996
|
6 |
3 |
p. 187-193
7 p.
|
artikel
|
| 23 |
Third International Congress on Human Mitochondrial Pathology (Euromit III): Towards a better understanding of energy metabolism disorders
|
Possekel, S.
|
|
1996
|
6 |
3 |
p. 215-218
4 p.
|
artikel
|
| 24 |
Trigeminal neuralgia, a practical approach to management
|
Bone, Ian
|
|
1996
|
6 |
3 |
p. 221-222
2 p.
|
artikel
|
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