| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Basic neurology, 2nd Edn
|
Stark, Gordon D.
|
|
1991
|
1 |
4 |
p. 313-314
2 p.
|
artikel
|
| 2 |
Benign muscular dystrophy with autosomal dominant inheritance
|
Somer, Hannu
|
|
1991
|
1 |
4 |
p. 267-273
7 p.
|
artikel
|
| 3 |
Carnitine acyltransferases in normal human skeletal muscle and in muscle of patients with carnitine palmitoyltransferase deficiency
|
Neumann-Schmidt, Sabine
|
|
1991
|
1 |
4 |
p. 253-260
8 p.
|
artikel
|
| 4 |
Clinical and genetic heterogeneity in spinal muscular atrophy—the multiple allele model
|
Emery, Alan E.H.
|
|
1991
|
1 |
4 |
p. 307-308
2 p.
|
artikel
|
| 5 |
Comprehensive neurology
|
Davidson, D.L.W.
|
|
1991
|
1 |
4 |
p. 316-
1 p.
|
artikel
|
| 6 |
Diagnostic criteria for facioscapulohumeral muscular dystrophy
|
Padberg, G.W.
|
|
1991
|
1 |
4 |
p. 231-234
4 p.
|
artikel
|
| 7 |
Different gene loci for hyperkalemic and hypokalemic periodic paralysis
|
Fontaine, Bertrand
|
|
1991
|
1 |
4 |
p. 235-238
4 p.
|
artikel
|
| 8 |
EAMDA news
|
|
|
1991
|
1 |
4 |
p. 319-
1 p.
|
artikel
|
| 9 |
Guillain-Barré syndrome
|
Stark, Gordon D.
|
|
1991
|
1 |
4 |
p. 314-
1 p.
|
artikel
|
| 10 |
Handedness and developmental disorder
|
Sofaer, J.A.
|
|
1991
|
1 |
4 |
p. 314-315
2 p.
|
artikel
|
| 11 |
Imaging methods reveal unexpected patchy lesions in late onset distal myopathy
|
Udd, Bjarne
|
|
1991
|
1 |
4 |
p. 279-285
7 p.
|
artikel
|
| 12 |
Introduction to risk calculation in genetic counselling
|
Mueller, R.F.
|
|
1991
|
1 |
4 |
p. 316-317
2 p.
|
artikel
|
| 13 |
Late onset lipid storage myopathy due to multiple acyl CoA dehydrogenase deficiency triggered by valproate
|
Papadimitriou, Alexandros
|
|
1991
|
1 |
4 |
p. 247-252
6 p.
|
artikel
|
| 14 |
Molecular genetics in diseases in brain, nerve and muscle
|
John Grindle, C.F.
|
|
1991
|
1 |
4 |
p. 313-
1 p.
|
artikel
|
| 15 |
Neurology in clinical practice
|
Matthews, W.B.
|
|
1991
|
1 |
4 |
p. 315-316
2 p.
|
artikel
|
| 16 |
Neuromuscular disorders: gene location
|
|
|
1991
|
1 |
4 |
p. 309-311
3 p.
|
artikel
|
| 17 |
Peripheral mechanisms of fatigue in muscles of normal and dystrophic mice
|
Pagala, Murali K.D.
|
|
1991
|
1 |
4 |
p. 287-298
12 p.
|
artikel
|
| 18 |
Steroids in duchenne muscular dystrophy — Deflazacort trial
|
Mesa, L.E.
|
|
1991
|
1 |
4 |
p. 261-266
6 p.
|
artikel
|
| 19 |
4th Colloquium on neuromuscular diseases (24–28 June 1991, Montpellier, France)
|
Schwartz, K.
|
|
1991
|
1 |
4 |
p. 299-304
6 p.
|
artikel
|
| 20 |
The adult spine: Principles and practice
|
Hughes, Sean P.F.
|
|
1991
|
1 |
4 |
p. 317-
1 p.
|
artikel
|
| 21 |
The Gaetano Conte Academy
|
|
|
1991
|
1 |
4 |
p. 305-
1 p.
|
artikel
|
| 22 |
X-linked and FSH dystrophies in one family
|
Lecky, B.R.F.
|
|
1991
|
1 |
4 |
p. 275-278
4 p.
|
artikel
|
| 23 |
X-linked centronuclear myopathy: Mapping the gene to Xq28
|
Liechti-Gallati, S.
|
|
1991
|
1 |
4 |
p. 239-245
7 p.
|
artikel
|
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