| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of bulbar type cerebral palsy: Representative symptoms of dorsal brainstem syndrome
|
Hiyane, Masato
|
|
2012
|
34 |
9 |
p. 787-791
5 p.
|
artikel
|
| 2 |
A case of malignant migrating partial seizures in infancy as a continuum of infantile epileptic encephalopathy
|
Lee, Eun Hye
|
|
2012
|
34 |
9 |
p. 768-772
5 p.
|
artikel
|
| 3 |
A developmental change of the visual behavior of the face recognition in the early infancy
|
Konishi, Yukihiko
|
|
2012
|
34 |
9 |
p. 719-722
4 p.
|
artikel
|
| 4 |
An immunologic case study of acute encephalitis with refractory, repetitive partial seizures
|
Wakamoto, Hiroyuki
|
|
2012
|
34 |
9 |
p. 763-767
5 p.
|
artikel
|
| 5 |
Announcements and reports
|
|
|
2012
|
34 |
9 |
p. II-VI
nvt p.
|
artikel
|
| 6 |
A pediatric case of reversible cerebral vasoconstriction syndrome with cortical subarachnoid hemorrhage
|
Yoshioka, Seiichiro
|
|
2012
|
34 |
9 |
p. 796-798
3 p.
|
artikel
|
| 7 |
Childhood-onset anti-MuSK antibody positive myasthenia gravis demonstrates a distinct clinical course
|
Takahashi, Yumi
|
|
2012
|
34 |
9 |
p. 784-786
3 p.
|
artikel
|
| 8 |
Clinical study in Chinese patients with late-infantile form neuronal ceroid lipofuscinoses
|
Chang, Xingzhi
|
|
2012
|
34 |
9 |
p. 739-745
7 p.
|
artikel
|
| 9 |
Congenital abnormalities in Japanese patients with Menkes disease
|
Gu, Yan-Hong
|
|
2012
|
34 |
9 |
p. 746-749
4 p.
|
artikel
|
| 10 |
Contents
|
|
|
2012
|
34 |
9 |
p. OBC-
1 p.
|
artikel
|
| 11 |
Contents continued
|
|
|
2012
|
34 |
9 |
p. IBC-
1 p.
|
artikel
|
| 12 |
Development of the human abducens nucleus: A morphometric study
|
Yamaguchi, Katsuyuki
|
|
2012
|
34 |
9 |
p. 712-718
7 p.
|
artikel
|
| 13 |
Editorial Board
|
|
|
2012
|
34 |
9 |
p. IFC-
1 p.
|
artikel
|
| 14 |
Efficacy and tolerance of gastrostomy feeding in Japanese muscular dystrophy patients
|
Mizuno, Tomoko
|
|
2012
|
34 |
9 |
p. 756-762
7 p.
|
artikel
|
| 15 |
Focal EEG abnormalities might reflect neuropathological characteristics of pervasive developmental disorder and attention-deficit/hyperactivity disorder
|
Kawatani, Masao
|
|
2012
|
34 |
9 |
p. 723-730
8 p.
|
artikel
|
| 16 |
Hypoyelination in I-cell disease; MRI, MR spectroscopy and neuropathological correlation
|
Takanashi, Jun-ichi
|
|
2012
|
34 |
9 |
p. 780-783
4 p.
|
artikel
|
| 17 |
Long-term developmental outcome in patients with West syndrome after epilepsy surgery
|
Iwatani, Yoshiko
|
|
2012
|
34 |
9 |
p. 731-738
8 p.
|
artikel
|
| 18 |
Molecular diagnostic dilemmas in Rett syndrome
|
Zvereff, Val
|
|
2012
|
34 |
9 |
p. 750-755
6 p.
|
artikel
|
| 19 |
Novel AGTR2 missense mutation in a Japanese boy with severe mental retardation, pervasive developmental disorder, and epilepsy
|
Takeshita, Eri
|
|
2012
|
34 |
9 |
p. 776-779
4 p.
|
artikel
|
| 20 |
Ring chromosome 21 in the differential diagnosis of waddling gait
|
Arslan, Mutluay
|
|
2012
|
34 |
9 |
p. 792-795
4 p.
|
artikel
|
| 21 |
Subacute sclerosing panencephalitis (SSPE) the story of a vanishing disease
|
Gadoth, Natan
|
|
2012
|
34 |
9 |
p. 705-711
7 p.
|
artikel
|
| 22 |
The 2013 JSCN International Education Fellowship
|
|
|
2012
|
34 |
9 |
p. I-
1 p.
|
artikel
|
| 23 |
Transient reduced diffusion in the cortex in a child with prolonged febrile seizures
|
Kato, Toru
|
|
2012
|
34 |
9 |
p. 773-775
3 p.
|
artikel
|
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