| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A further family with epilepsy, dementia and yellow teeth: the Kohlschütter syndrome
|
Musumeci, Sebastiano Antonino
|
|
1995
|
17 |
2 |
p. 133-138
6 p.
|
artikel
|
| 2 |
Clinical and MRI findings in a case ofd-2-hydroxyglutaric aciduria
|
Sugita, Katsuo
|
|
1995
|
17 |
2 |
p. 139-141
3 p.
|
artikel
|
| 3 |
Cranial haemorrhage in the term newborn infant
|
Takashima, Sachia
|
|
1995
|
17 |
2 |
p. 155-
1 p.
|
artikel
|
| 4 |
Deficiency in complex IV (cytochrome c oxidase) of the respiratory chain, presenting as a leukodystrophy in two siblings with Leigh syndrome
|
Zafeiriou, Dimitrios I.
|
|
1995
|
17 |
2 |
p. 117-121
5 p.
|
artikel
|
| 5 |
Developmental perspective of sensory organization on postural control
|
Hirabayashi, Shin-ichi
|
|
1995
|
17 |
2 |
p. 111-113
3 p.
|
artikel
|
| 6 |
Epidermal nevus syndrome with isolated enlargement of one temporal lobe: a case report
|
Kwa, Vincent I.H.
|
|
1995
|
17 |
2 |
p. 122-125
4 p.
|
artikel
|
| 7 |
Epilepsy, dementia and yellow teeth: some remarks on multiorgan involvement in neurogenetic disorders commentary to Musumeci's paper (Brain Dev 1995;17 133–138)
|
Kohlschütter, Alfried
|
|
1995
|
17 |
2 |
p. 142-143
2 p.
|
artikel
|
| 8 |
2-Hydroxyglutaric acidurias commentary to Sugito's paper (Brain Dev 1995;17: 139-41)
|
Barth, Peter G.
|
|
1995
|
17 |
2 |
p. 144-145
2 p.
|
artikel
|
| 9 |
Hyperekplexia, a cause of neonatal apnea: a case report
|
Dias Gherpelli, JoséLuiz
|
|
1995
|
17 |
2 |
p. 114-116
3 p.
|
artikel
|
| 10 |
Hyperkinetic behaviour and superimposed concepts response to De Negri's commentary (Brain Dev 1995:17: 146-7)
|
Gordon, Neil
|
|
1995
|
17 |
2 |
p. 148-
1 p.
|
artikel
|
| 11 |
Hyperkinetic behaviour, attention deficit disorder, conduct disorder and instabilitépsychomotrice: identity, analogies, and misunderstandings commentary to Gordon's paper (Brain Dev 1994;15: 169-72)
|
De Negri, Maurizio
|
|
1995
|
17 |
2 |
p. 146-147
2 p.
|
artikel
|
| 12 |
123I-IMP SPECT findings in mitochondrial encephalomyopathies
|
Fujii, Tatsuya
|
|
1995
|
17 |
2 |
p. 89-94
6 p.
|
artikel
|
| 13 |
Inhibitory period and late muscular responses after transcranial magnetic stimulation in healthy children
|
Masur, Harald
|
|
1995
|
17 |
2 |
p. 149-152
4 p.
|
artikel
|
| 14 |
Morphometric study of the corpus callosum in Fukuyama type congenital muscular dystrophy by magnetic resonance imaging
|
Wang, Zhi-Ping
|
|
1995
|
17 |
2 |
p. 104-110
7 p.
|
artikel
|
| 15 |
Muscle CT scans in preclinical cases of Duchenne and Becker muscular dystrophy
|
Arai, Yumi
|
|
1995
|
17 |
2 |
p. 95-103
9 p.
|
artikel
|
| 16 |
Olivopontocerebellar atrophy: a case report
|
Pemde, Harish K.
|
|
1995
|
17 |
2 |
p. 130-132
3 p.
|
artikel
|
| 17 |
Personnel
|
|
|
1995
|
17 |
2 |
p. 156-
1 p.
|
artikel
|
| 18 |
Poliomyelitis-like illness after acute asthma (Hopkins syndrome): a histological study of biopsied muscle in a case
|
Mizuno, Yoshihiko
|
|
1995
|
17 |
2 |
p. 126-129
4 p.
|
artikel
|
| 19 |
Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approach
|
Goebel, Hans H.
|
|
1995
|
17 |
2 |
p. 83-88
6 p.
|
artikel
|
| 20 |
Schedule of meetings
|
|
|
1995
|
17 |
2 |
p. 156-158
3 p.
|
artikel
|
| 21 |
The management of visual impairment in childhood. Clinics in developmental medicine, No. 128
|
Harada, Masami
|
|
1995
|
17 |
2 |
p. 155-
1 p.
|
artikel
|
| 22 |
The prevalence of Rett syndrome in Fukui prefecture
|
Terai, Katsuyuki
|
|
1995
|
17 |
2 |
p. 153-154
2 p.
|
artikel
|
Tijdschrift beschrijving