| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Amyotrophic lateral sclerosis: A comprehensive guide to management
|
Shaw, Pamela J.
|
|
1997
|
7 |
3 |
p. 208-209
2 p.
|
artikel
|
| 2 |
Clinical pediatric neurology: A sign and symptoms approach E3
|
Eunson, Paul
|
|
1997
|
7 |
3 |
p. 209-
1 p.
|
artikel
|
| 3 |
Congenital myopathy with excess of thin myofilaments
|
Goebel, Hans H.
|
|
1997
|
7 |
3 |
p. 160-168
9 p.
|
artikel
|
| 4 |
Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy
|
Ishii, Hiroko
|
|
1997
|
7 |
3 |
p. 191-197
7 p.
|
artikel
|
| 5 |
External ophthalmoplegia in neuromuscular disorders: Case report and review of the literature
|
Jones, Kristi J.
|
|
1997
|
7 |
3 |
p. 143-151
9 p.
|
artikel
|
| 6 |
Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotype
|
Talbot, Kevin
|
|
1997
|
7 |
3 |
p. 198-201
4 p.
|
artikel
|
| 7 |
Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis
|
Guicheney, Pascale
|
|
1997
|
7 |
3 |
p. 180-186
7 p.
|
artikel
|
| 8 |
Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matter
|
Echenne, B.
|
|
1997
|
7 |
3 |
p. 187-190
4 p.
|
artikel
|
| 9 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
1997
|
7 |
3 |
p. XII-XVII
nvt p.
|
artikel
|
| 10 |
Mitochondrial tRNACys gene mutation (A5814G): a second family with mitochondrial encephalopathy
|
Santorelli, Filippo M.
|
|
1997
|
7 |
3 |
p. 156-159
4 p.
|
artikel
|
| 11 |
Neuromuscular disorders: gene location
|
|
|
1997
|
7 |
3 |
p. I-XI
nvt p.
|
artikel
|
| 12 |
Prenatal diagnosis in merosin-deficient congenital muscular dystrophy
|
Naom, Isam
|
|
1997
|
7 |
3 |
p. 176-179
4 p.
|
artikel
|
| 13 |
Spinal muscular atrophy—clinical and genetic correlations
|
Zerres, Klaus
|
|
1997
|
7 |
3 |
p. 202-207
6 p.
|
artikel
|
| 14 |
The Cambridge illustrated history of medicine
|
Emery, Alan
|
|
1997
|
7 |
3 |
p. 208-
1 p.
|
artikel
|
| 15 |
Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin α2 chain
|
Sewry, C.A.
|
|
1997
|
7 |
3 |
p. 169-175
7 p.
|
artikel
|
| 16 |
Variation of CTG-repeat number of the DMPK gene in muscle tissue
|
Ansved, T.
|
|
1997
|
7 |
3 |
p. 152-155
4 p.
|
artikel
|
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