nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('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 |
artikel |
2 |
A case of delayed diagnosis of Becker muscular dystrophy due to underlying developmental disorders
|
Oda, Shinji |
|
|
44 |
3 |
p. 259-262 |
artikel |
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 |
artikel |
4 |
Acknowledgments to Anonymous Reviewers in 2021
|
|
|
|
44 |
3 |
p. I-III |
artikel |
5 |
Acute encephalopathy with biphasic seizures and late reduced diffusion: Predictive EEG findings
|
Ohno, Atsuko |
|
|
44 |
3 |
p. 221-228 |
artikel |
6 |
An autopsy case of recurrent pneumothorax and peliosis-like intrapulmonary hematoma with X-linked myotubular myopathy
|
Yabe, Tomona |
|
|
44 |
3 |
p. 234-238 |
artikel |
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 |
artikel |
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 |
artikel |
9 |
Contents
|
|
|
|
44 |
3 |
p. OBC |
artikel |
10 |
Cover
|
|
|
|
44 |
3 |
p. IBC |
artikel |
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 |
artikel |
12 |
Editorial Board
|
|
|
|
44 |
3 |
p. IFC |
artikel |
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 |
artikel |
14 |
Hemorrhagic shock and encephalopathy syndrome in a patient with a de novo heterozygous variant in KIF1A
|
Isobe, Kouji |
|
|
44 |
3 |
p. 249-253 |
artikel |
15 |
Intravenous ketogenic diet therapy for neonatal-onset pyruvate dehydrogenase complex deficiency
|
Inui, Takehiko |
|
|
44 |
3 |
p. 244-248 |
artikel |
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 |
artikel |