| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Alpha-actinin in nemaline bodies in congenital nemaline myopathy: immunological confirmation by light and electron microscopy
|
Wallgren-Pettersson, Carina
|
|
|
5 |
2 |
p. 93-104
|
artikel
|
| 2 |
Chronic fatigue syndromes: The limbic hypothesis
|
Hudgson, P.
|
|
|
5 |
2 |
p. 167-168
|
artikel
|
| 3 |
Coexistence of scleromyositis associated with PM-SCL antibody and myasthenia
|
Hausmanowa-Petrusewicz, I.
|
|
|
5 |
2 |
p. 145-147
|
artikel
|
| 4 |
Companion encyclopedia of the history of medicine
|
Emery, Alan
|
|
|
5 |
2 |
p. 168-169
|
artikel
|
| 5 |
Desmin in myology 24th European Neuromuscular Center-sponsored workshop held 5–6 November 1993, Naarden, The Netherlands
|
Goebel, H.H.
|
|
|
5 |
2 |
p. 161-166
|
artikel
|
| 6 |
Differential diagnosis of periodic paralysis aided by in vitro myography
|
Iaizzo, Paul A.
|
|
|
5 |
2 |
p. 115-124
|
artikel
|
| 7 |
Discordant clinical outcome in myotonic dystrophy relatives showing (CTG) n > 700 repeats
|
Novelli, G.
|
|
|
5 |
2 |
p. 157-159
|
artikel
|
| 8 |
Familial myopathy with conspicuous depletion of mitochondria in muscle fibers: a morphologically distinct disease
|
Genge, Angela
|
|
|
5 |
2 |
p. 139-144
|
artikel
|
| 9 |
Intramembrane charge movements in striated muscle
|
Weir, Andrew I.
|
|
|
5 |
2 |
p. 169-170
|
artikel
|
| 10 |
Malignant hyperthermia susceptibility without central core disease (CCD) in a family where CCD is diagnosed
|
Islander, Gunilla
|
|
|
5 |
2 |
p. 125-127
|
artikel
|
| 11 |
Mitochondrial encephalomyopathies: Gene mutation
|
|
|
|
5 |
2 |
p. V-VI
|
artikel
|
| 12 |
Neonatal carnitine palmitoyltransferase-2 deficiency: a case presenting with myopathy
|
Land, John M.
|
|
|
5 |
2 |
p. 129-137
|
artikel
|
| 13 |
Neurological examination made easy
|
Stark, Gordon
|
|
|
5 |
2 |
p. 169
|
artikel
|
| 14 |
Neurological rehabilitation
|
Edwards, Richard
|
|
|
5 |
2 |
p. 167
|
artikel
|
| 15 |
Neuromuscular disorders: Gene location
|
|
|
|
5 |
2 |
p. I-IV
|
artikel
|
| 16 |
Sarcolemmal expression of dystrophin C-terminus but reduced expression of 6q-dystrophin-related protein in two DMD patients with large deletions of the dystrophin gene
|
Bittner, Reginald E.
|
|
|
5 |
2 |
p. 81-92
|
artikel
|
| 17 |
Sarcolemmal indentation in cardiomyopathy with mental retardation and vacuolar myopathy
|
Murakami, Nobuyuki
|
|
|
5 |
2 |
p. 149-155
|
artikel
|
| 18 |
The effect of glucocorticoids on the accumulation of utrophin by cultured normal and dystrophic human skeletal muscle satellite cells
|
Pasquini, F.
|
|
|
5 |
2 |
p. 105-114
|
artikel
|
Tijdschrift beschrijving