| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Announcements and reports
|
|
|
2015
|
37 |
9 |
p. I-IV
nvt p.
|
artikel
|
| 2 |
ATP1A3 mutation in a Chinese girl with alternating hemiplegia of childhood – Potential target of treatment?
|
Wong, Virginia C.N.
|
|
2015
|
37 |
9 |
p. 907-910
4 p.
|
artikel
|
| 3 |
Call for papers
|
|
|
2015
|
37 |
9 |
p. V-
1 p.
|
artikel
|
| 4 |
Characteristic MRI features of chronic inflammatory demyelinating polyradiculoneuropathy
|
Abe, Yuichi
|
|
2015
|
37 |
9 |
p. 894-896
3 p.
|
artikel
|
| 5 |
Clinical features and long-term outcome of a group of Japanese children with inflammatory central nervous system disorders and seropositivity to myelin-oligodendrocyte glycoprotein antibodies
|
Hino-Fukuyo, Naomi
|
|
2015
|
37 |
9 |
p. 849-852
4 p.
|
artikel
|
| 6 |
Contents
|
|
|
2015
|
37 |
9 |
p. OBC-
1 p.
|
artikel
|
| 7 |
Cover
|
|
|
2015
|
37 |
9 |
p. IBC-
1 p.
|
artikel
|
| 8 |
Developmental trajectories for attention and working memory in healthy Japanese school-aged children
|
Egami, Chiyomi
|
|
2015
|
37 |
9 |
p. 840-848
9 p.
|
artikel
|
| 9 |
Editorial Board
|
|
|
2015
|
37 |
9 |
p. IFC-
1 p.
|
artikel
|
| 10 |
Efficacy and safety of fosphenytoin for benign convulsions with mild gastroenteritis
|
Nakazawa, Mika
|
|
2015
|
37 |
9 |
p. 864-867
4 p.
|
artikel
|
| 11 |
Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients
|
Yang, Haipo
|
|
2015
|
37 |
9 |
p. 880-886
7 p.
|
artikel
|
| 12 |
Late-onset epileptic spasms in a female patient with a CASK mutation
|
Nakajiri, Tomoshi
|
|
2015
|
37 |
9 |
p. 919-923
5 p.
|
artikel
|
| 13 |
Mixed movements disorders as an initial feature of pediatric lupus
|
Mrabet, Saloua
|
|
2015
|
37 |
9 |
p. 904-906
3 p.
|
artikel
|
| 14 |
Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state
|
Kawase, Koya
|
|
2015
|
37 |
9 |
p. 887-890
4 p.
|
artikel
|
| 15 |
New phenotype and neonatal onset of sodium channel myotonia in a child with a novel mutation of SCN4A gene
|
Fusco, Carlo
|
|
2015
|
37 |
9 |
p. 891-893
3 p.
|
artikel
|
| 16 |
Paroxysmal nonepileptic motor phenomena in newborn
|
Orivoli, Sonia
|
|
2015
|
37 |
9 |
p. 833-839
7 p.
|
artikel
|
| 17 |
Predictive value of paroxysmal EEG abnormalities for future epilepsy in focal febrile seizures
|
Gradisnik, Peter
|
|
2015
|
37 |
9 |
p. 868-873
6 p.
|
artikel
|
| 18 |
Relationship between stature and tibial length for children with moderate-to-severe cerebral palsy
|
Kihara, Kenji
|
|
2015
|
37 |
9 |
p. 853-857
5 p.
|
artikel
|
| 19 |
Somatic mosaicism of a CDKL5 mutation identified by next-generation sequencing
|
Kato, Takeshi
|
|
2015
|
37 |
9 |
p. 911-915
5 p.
|
artikel
|
| 20 |
Subacute sclerosing panencephalitis with parkinsonian features in a child: A case report
|
Bozlu, Gulcin
|
|
2015
|
37 |
9 |
p. 901-903
3 p.
|
artikel
|
| 21 |
Successful control of radicular pain in a pediatric patient with Guillain–Barré syndrome
|
Kajimoto, Madoka
|
|
2015
|
37 |
9 |
p. 897-900
4 p.
|
artikel
|
| 22 |
Surgical treatment for medically refractory focal epilepsy in a patient with fragile X syndrome
|
Kenmuir, Cynthia
|
|
2015
|
37 |
9 |
p. 916-918
3 p.
|
artikel
|
| 23 |
The neurological outcomes of cerebellar injury in premature infants
|
Kobayashi, Satoru
|
|
2015
|
37 |
9 |
p. 858-863
6 p.
|
artikel
|
| 24 |
Three patients manifesting early infantile epileptic spasms associated with 2q24.3 microduplications
|
Yoshitomi, Shinsaku
|
|
2015
|
37 |
9 |
p. 874-879
6 p.
|
artikel
|
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