| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A case of bilateral limbic and recurrent unilateral cortical encephalitis with anti-myelin oligodendrocyte glycoprotein antibody positivity
|
Horita, Takahiro
|
|
|
44 |
3 |
p. 254-258
|
article
|
| 2 |
A case of delayed diagnosis of Becker muscular dystrophy due to underlying developmental disorders
|
Oda, Shinji
|
|
|
44 |
3 |
p. 259-262
|
article
|
| 3 |
A case with congenital disorder of glycosylation with defective fucosylation 2 and new mutation in FUK gene
|
Özgün, Nezir
|
|
|
44 |
3 |
p. 239-243
|
article
|
| 4 |
Acknowledgments to Anonymous Reviewers in 2021
|
|
|
|
44 |
3 |
p. I-III
|
article
|
| 5 |
Acute encephalopathy with biphasic seizures and late reduced diffusion: Predictive EEG findings
|
Ohno, Atsuko
|
|
|
44 |
3 |
p. 221-228
|
article
|
| 6 |
An autopsy case of recurrent pneumothorax and peliosis-like intrapulmonary hematoma with X-linked myotubular myopathy
|
Yabe, Tomona
|
|
|
44 |
3 |
p. 234-238
|
article
|
| 7 |
Boys with attention-deficit/hyperactivity disorder perform wider and fewer finger tapping than typically developing boys – Peer comparisons and the effects of methylphenidate from an exploratory perspective
|
Enokizono, Takashi
|
|
|
44 |
3 |
p. 189-195
|
article
|
| 8 |
Breastfeeding and risk of febrile seizures in the first 3 years of life: The Japan Environment and Children’s Study
|
Mitsuda, Naomi
|
|
|
44 |
3 |
p. 203-209
|
article
|
| 9 |
Contents
|
|
|
|
44 |
3 |
p. OBC
|
article
|
| 10 |
Cover
|
|
|
|
44 |
3 |
p. IBC
|
article
|
| 11 |
Creatinine-to-cystatin C ratio estimates muscle mass correlating the markers of the patients with severe motor and intellectual disabilities
|
Nakahara, Hirotomo
|
|
|
44 |
3 |
p. 196-202
|
article
|
| 12 |
Editorial Board
|
|
|
|
44 |
3 |
p. IFC
|
article
|
| 13 |
Growth and differentiation factor-15 as a potential prognostic biomarker for status-epilepticus-associated-with-fever: A pilot study
|
Yamaguchi, Hiroshi
|
|
|
44 |
3 |
p. 210-220
|
article
|
| 14 |
Hemorrhagic shock and encephalopathy syndrome in a patient with a de novo heterozygous variant in KIF1A
|
Isobe, Kouji
|
|
|
44 |
3 |
p. 249-253
|
article
|
| 15 |
Intravenous ketogenic diet therapy for neonatal-onset pyruvate dehydrogenase complex deficiency
|
Inui, Takehiko
|
|
|
44 |
3 |
p. 244-248
|
article
|
| 16 |
Neuropsychological and neurophysiological features of WAGR syndrome: Detailed comprehensive evaluation of a patient with severe intellectual disability and autism spectrum disorder
|
Nishizawa, Hitomi
|
|
|
44 |
3 |
p. 229-233
|
article
|
Journal description