| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of Canavan disease with microcephaly
|
Gowda, Vykuntaraju K.
|
|
2016
|
38 |
8 |
p. 759-762
4 p.
|
artikel
|
| 2 |
Acute encephalitis with refractory, repetitive partial seizures: Pathological findings and a new therapeutic approach using tacrolimus
|
Sato, Yuko
|
|
2016
|
38 |
8 |
p. 772-776
5 p.
|
artikel
|
| 3 |
Announcements and reports
|
|
|
2016
|
38 |
8 |
p. I-III
nvt p.
|
artikel
|
| 4 |
A novel gene mutation in PANK2 in a patient with severe jaw-opening dystonia
|
Yapici, Zuhal
|
|
2016
|
38 |
8 |
p. 755-758
4 p.
|
artikel
|
| 5 |
A novel PIGA mutation in a family with X-linked, early-onset epileptic encephalopathy
|
Kim, Young Ok
|
|
2016
|
38 |
8 |
p. 750-754
5 p.
|
artikel
|
| 6 |
Applicability of the Movement Assessment Battery for Children-Second Edition to Japanese children: A study of the Age Band 2
|
Kita, Yosuke
|
|
2016
|
38 |
8 |
p. 706-713
8 p.
|
artikel
|
| 7 |
Contents
|
|
|
2016
|
38 |
8 |
p. OBC-
1 p.
|
artikel
|
| 8 |
Corrigendum to “Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene” [Brain Dev. 38 (2016) 167–172]
|
Castro-Gago, Manuel
|
|
2016
|
38 |
8 |
p. 783-
1 p.
|
artikel
|
| 9 |
Corrigendum to “Efficacy and tolerability of high-dose phenobarbital in children with focal seizures” [Brain Dev. 38 (2016) 414–418]
|
Okumura, Akihisa
|
|
2016
|
38 |
8 |
p. 784-
1 p.
|
artikel
|
| 10 |
Cover
|
|
|
2016
|
38 |
8 |
p. IBC-
1 p.
|
artikel
|
| 11 |
Diffusion restriction in ethylmalonic encephalopathy – An imaging evidence of the pathophysiology of the disease
|
Bhat, Maya Dattatraya
|
|
2016
|
38 |
8 |
p. 768-771
4 p.
|
artikel
|
| 12 |
Editorial Board
|
|
|
2016
|
38 |
8 |
p. IFC-
1 p.
|
artikel
|
| 13 |
JSCM Call for Papers 2017
|
|
|
2016
|
38 |
8 |
p. IV-
1 p.
|
artikel
|
| 14 |
Mucolipidosis IV: A milder form with novel mutations and serial MRI findings
|
Shiihara, Takashi
|
|
2016
|
38 |
8 |
p. 763-767
5 p.
|
artikel
|
| 15 |
Neonatal screening for Menkes disease using urine HVA/VMA ratio
|
Matsuo, Muneaki
|
|
2016
|
38 |
8 |
p. 781-
1 p.
|
artikel
|
| 16 |
Refractory and severe status epilepticus in a patient with ring chromosome 20 syndrome
|
Hirano, Yoshiko
|
|
2016
|
38 |
8 |
p. 746-749
4 p.
|
artikel
|
| 17 |
Reply to the letter: “Neonatal screening for Menkes disease using urine HVA/VMA ratio”
|
Yagi, Mariko
|
|
2016
|
38 |
8 |
p. 782-
1 p.
|
artikel
|
| 18 |
Self-concept in children and adolescents with epilepsy: The role of family functioning, mothers’ emotional symptoms and ADHD
|
Ekinci, Ozalp
|
|
2016
|
38 |
8 |
p. 714-722
9 p.
|
artikel
|
| 19 |
Short and long-term outcomes in children with suspected acute encephalopathy
|
Nishiyama, Masahiro
|
|
2016
|
38 |
8 |
p. 731-737
7 p.
|
artikel
|
| 20 |
Staurosporine allows dystrophin expression by skipping of nonsense-encoding exon
|
Nishida, Atsushi
|
|
2016
|
38 |
8 |
p. 738-745
8 p.
|
artikel
|
| 21 |
Stem cells therapy in cerebral palsy: A systematic review
|
Kułak-Bejda, Agnieszka
|
|
2016
|
38 |
8 |
p. 699-705
7 p.
|
artikel
|
| 22 |
The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy
|
Takeuchi, Tomoya
|
|
2016
|
38 |
8 |
p. 723-730
8 p.
|
artikel
|
| 23 |
Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation
|
Sell, Katharina
|
|
2016
|
38 |
8 |
p. 777-780
4 p.
|
artikel
|
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