no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
Acknowledgments to Anonymous Reviewers in 2013
|
|
|
2014 |
36 |
3 |
p. VI-VII nvt p. |
article |
2 |
A de novo CASK mutation in pontocerebellar hypoplasia type 3 with early myoclonic epilepsy and tetralogy of Fallot
|
Nakamura, Kazuyuki |
|
2014 |
36 |
3 |
p. 272-273 2 p. |
article |
3 |
Announcements and reports
|
|
|
2014 |
36 |
3 |
p. I-V nvt p. |
article |
4 |
Contents
|
|
|
2014 |
36 |
3 |
p. OBC- 1 p. |
article |
5 |
Different patterns of cerebellar abnormality and hypomyelination between POLR3A and POLR3B mutations
|
Takanashi, Jun-ichi |
|
2014 |
36 |
3 |
p. 259-263 5 p. |
article |
6 |
Early replacement therapy in a first Japanese case with autosomal recessive guanosine triphosphate cyclohydrolase I deficiency with a novel point mutation
|
Sato, Hiroki |
|
2014 |
36 |
3 |
p. 268-271 4 p. |
article |
7 |
Editorial Board
|
|
|
2014 |
36 |
3 |
p. IFC- 1 p. |
article |
8 |
Effect of maternal micronutrients (folic acid and vitamin B12) and omega 3 fatty acids on indices of brain oxidative stress in the offspring
|
Roy, Suchitra |
|
2014 |
36 |
3 |
p. 219-227 9 p. |
article |
9 |
Epilepsy associated with autism and attention deficit hyperactivity disorder: Is there a genetic link?
|
Lo-Castro, Adriana |
|
2014 |
36 |
3 |
p. 185-193 9 p. |
article |
10 |
IBC
|
|
|
2014 |
36 |
3 |
p. IBC- 1 p. |
article |
11 |
Impaired exploratory eye movements in children with Asperger’s syndrome
|
Ohya, Takashi |
|
2014 |
36 |
3 |
p. 241-247 7 p. |
article |
12 |
Impaired function of the auditory brainstem in term neonates with hyperbilirubinemia
|
Jiang, Ze D. |
|
2014 |
36 |
3 |
p. 212-218 7 p. |
article |
13 |
Paraneoplastic neurological disorders in children with benign ovarian tumors
|
Hsu, Mei-Hsin |
|
2014 |
36 |
3 |
p. 248-253 6 p. |
article |
14 |
Preconditioning and post-treatment with cobalt chloride in rat model of perinatal hypoxic–ischemic encephalopathy
|
Dai, Ying |
|
2014 |
36 |
3 |
p. 228-240 13 p. |
article |
15 |
Prenatal diagnosis of citrullinemia type 1: A Chinese family with a novel mutation of the ASS1 gene
|
Wu, Tong-Fei |
|
2014 |
36 |
3 |
p. 264-267 4 p. |
article |
16 |
Role of cerebral ultrasound and magnetic resonance imaging in newborns with congenital cytomegalovirus infection
|
Capretti, Maria Grazia |
|
2014 |
36 |
3 |
p. 203-211 9 p. |
article |
17 |
The efficacy of gabapentin in children of partial seizures and the blood levels
|
Nonoda, Yutaka |
|
2014 |
36 |
3 |
p. 194-202 9 p. |
article |
18 |
The ominous sequence in patients with tuberous sclerosis complex
|
Yamada, Hiroshi |
|
2014 |
36 |
3 |
p. 254-258 5 p. |
article |