| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case report of remarkable improvement of motor disturbances with l-dopa in a patient with post-diffuse axonal injury
|
Koeda, Tatsuya
|
|
1998
|
20 |
2 |
p. 124-126
3 p.
|
artikel
|
| 2 |
Benign partial epilepsy in infancy with complex partial seizures (Watanabe's syndrome): 12 non-Japanese new cases
|
Capovilla, Giuseppe
|
|
1998
|
20 |
2 |
p. 105-111
7 p.
|
artikel
|
| 3 |
Congenital muscular dystrophies: 1997 update
|
Voit, Thomas
|
|
1998
|
20 |
2 |
p. 65-74
10 p.
|
artikel
|
| 4 |
Increased levels of GM2 ganglioside in fibroblasts from a patient with juvenile Niemann–Pick disease type C
|
Watanabe, Yasuhiro
|
|
1998
|
20 |
2 |
p. 95-97
3 p.
|
artikel
|
| 5 |
Mechanisms of generalized absence epilepsy
|
Futatsugi, Yoshio
|
|
1998
|
20 |
2 |
p. 75-79
5 p.
|
artikel
|
| 6 |
Neuronal nuclear antigen (NeuN): a marker of neuronal maturation in the early human fetal nervous system 1 Presented at the XIII International Congress of Neuropathology, Perth, Australia, September 7–12, 1997. 1
|
Sarnat, Harvey B
|
|
1998
|
20 |
2 |
p. 88-94
7 p.
|
artikel
|
| 7 |
Neuropathological characteristics and alteration of the dopamine D2 receptor in hypoxic-ischemic basal ganglia necrosis
|
Meng, Shu Zhen
|
|
1998
|
20 |
2 |
p. 98-104
7 p.
|
artikel
|
| 8 |
Neuropsychological recovery from childhood moyamoya disease
|
Bowen, Matthew
|
|
1998
|
20 |
2 |
p. 119-123
5 p.
|
artikel
|
| 9 |
Panniculitis due to potassium bromide
|
Diener, Wilfried
|
|
1998
|
20 |
2 |
p. 83-87
5 p.
|
artikel
|
| 10 |
Paroxysmal tonic upgaze of childhood with ataxia: a benign transient dystonia with autosomal dominant inheritance
|
Guerrini, Renzo
|
|
1998
|
20 |
2 |
p. 116-118
3 p.
|
artikel
|
| 11 |
Reflex sympathetic dystrophy associated with deep peroneal nerve entrapment
|
Parano, Enrico
|
|
1998
|
20 |
2 |
p. 80-82
3 p.
|
artikel
|
| 12 |
Severe infantile congenital myopathy with nemaline and cytoplasmic bodies: a case report
|
Itakura, Yukino
|
|
1998
|
20 |
2 |
p. 112-115
4 p.
|
artikel
|
| 13 |
Trisomy 12p and epilepsy with myoclonic absences
|
Elia, Maurizio
|
|
1998
|
20 |
2 |
p. 127-130
4 p.
|
artikel
|
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