nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A case of acute encephalopathy with biphasic seizures and late reduced diffusion: Utility of arterial spin labeling sequence
|
Kuya, Keita |
|
2017 |
39 |
1 |
p. 84-88 5 p. |
artikel |
2 |
A case of Dravet syndrome with cortical myoclonus indicated by jerk-locked back-averaging of electroencephalogram data
|
Kobayashi, Yoshinori |
|
2017 |
39 |
1 |
p. 75-79 5 p. |
artikel |
3 |
A Japanese case of β-ureidopropionase deficiency with dysmorphic features
|
Akiyama, Tomoyuki |
|
2017 |
39 |
1 |
p. 58-61 4 p. |
artikel |
4 |
Announcements and reports
|
|
|
2017 |
39 |
1 |
p. I-IV nvt p. |
artikel |
5 |
Cerebral arteriopathy associated with heterozygous Arg179Cys mutation in the ACTA2 gene: Report in 2 newborn siblings
|
de Grazia, Jose |
|
2017 |
39 |
1 |
p. 62-66 5 p. |
artikel |
6 |
Contents
|
|
|
2017 |
39 |
1 |
p. OBC- 1 p. |
artikel |
7 |
Cover
|
|
|
2017 |
39 |
1 |
p. IBC- 1 p. |
artikel |
8 |
Editorial Board
|
|
|
2017 |
39 |
1 |
p. IFC- 1 p. |
artikel |
9 |
Efficacy of bezafibrate on fibroblasts of glutaric acidemia type II patients evaluated using an in vitro probe acylcarnitine assay
|
Yamada, Kenji |
|
2017 |
39 |
1 |
p. 48-57 10 p. |
artikel |
10 |
Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesis
|
Okazaki, Tetsuya |
|
2017 |
39 |
1 |
p. 67-71 5 p. |
artikel |
11 |
Longitudinal change in white matter in preterm infants without magnetic resonance imaging abnormalities: Assessment of serial diffusion tensor imaging and their relationship to neurodevelopmental outcomes
|
Kidowaki, Satoshi |
|
2017 |
39 |
1 |
p. 40-47 8 p. |
artikel |
12 |
Neurogenic muscle hypertrophy in a 12-year-old girl
|
Zutelija Fattorini, Matija |
|
2017 |
39 |
1 |
p. 89-92 4 p. |
artikel |
13 |
New guidelines for management of febrile seizures in Japan
|
Natsume, Jun |
|
2017 |
39 |
1 |
p. 2-9 8 p. |
artikel |
14 |
New year’s greetings: A Happy New Year 2017!
|
|
|
2017 |
39 |
1 |
p. 1- 1 p. |
artikel |
15 |
Prenatal irradiation–induced brain neuropathology and cognitive impairment
|
Yang, Bo |
|
2017 |
39 |
1 |
p. 10-22 13 p. |
artikel |
16 |
Quinidine therapy for West syndrome with KCNTI mutation: A case report
|
Fukuoka, Masataka |
|
2017 |
39 |
1 |
p. 80-83 4 p. |
artikel |
17 |
The pathology of incipient polymicrogyria
|
Diamandis, Phedias |
|
2017 |
39 |
1 |
p. 23-39 17 p. |
artikel |
18 |
Two mild cases of Dravet syndrome with truncating mutation of SCN1A
|
Takaori, Toru |
|
2017 |
39 |
1 |
p. 72-74 3 p. |
artikel |