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 |