| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Announcements and reports
|
|
|
2018
|
40 |
10 |
p. I-II
|
artikel
|
| 2 |
Anti-MOG antibody encephalitis mimicking neurological deterioration in a case of Rett syndrome with MECP2 mutation
|
Tani, Hiroo
|
|
2018
|
40 |
10 |
p. 943-946
|
artikel
|
| 3 |
A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features
|
Okumura, Akihisa
|
|
2018
|
40 |
10 |
p. 926-930
|
artikel
|
| 4 |
Contents
|
|
|
2018
|
40 |
10 |
p. OBC
|
artikel
|
| 5 |
Cover
|
|
|
2018
|
40 |
10 |
p. IBC
|
artikel
|
| 6 |
Editorial Board
|
|
|
2018
|
40 |
10 |
p. IFC
|
artikel
|
| 7 |
Fosphenytoin vs. continuous midazolam for pediatric febrile status epilepticus
|
Nishiyama, Masahiro
|
|
2018
|
40 |
10 |
p. 884-890
|
artikel
|
| 8 |
Genotypes and phenotypes in 20 Chinese patients with type 2 Gaucher disease
|
Kang, Lulu
|
|
2018
|
40 |
10 |
p. 876-883
|
artikel
|
| 9 |
Incidence of childhood epilepsy: A population-based study in rural Japan
|
Okamoto, Kentaro
|
|
2018
|
40 |
10 |
p. 904-908
|
artikel
|
| 10 |
Infantile spasms in a mosaic monocentric and duplicated SMC 15 patient
|
Isobe, Kiyotaka
|
|
2018
|
40 |
10 |
p. 891-896
|
artikel
|
| 11 |
Investigation of neuronal auto-antibodies in children diagnosed with epileptic encephalopathy of unknown cause
|
Tekturk, Pınar
|
|
2018
|
40 |
10 |
p. 909-917
|
artikel
|
| 12 |
Is hiragana decoding impaired in children with periventricular leukomalacia?
|
Kurahashi, Naoko
|
|
2018
|
40 |
10 |
p. 850-856
|
artikel
|
| 13 |
Loss of myelinated axons and astrocytosis in an autopsy case of acute encephalopathy with biphasic seizures and late reduced diffusion
|
Takanashi, Jun-ichi
|
|
2018
|
40 |
10 |
p. 947-951
|
artikel
|
| 14 |
Migraine and associated comorbidities are three times more frequent in children with ADHD and their mothers
|
Kutuk, Meryem Ozlem
|
|
2018
|
40 |
10 |
p. 857-864
|
artikel
|
| 15 |
Neurochemistry evaluated by MR spectroscopy in a patient with xeroderma pigmentosum group A
|
Yokota, Kana
|
|
2018
|
40 |
10 |
p. 931-933
|
artikel
|
| 16 |
Nonketotic hyperglycinemia: Clinical range and outcome of a rare neurometabolic disease in a single-center
|
Genç Sel, Çiğdem
|
|
2018
|
40 |
10 |
p. 865-875
|
artikel
|
| 17 |
Novel IARS2 mutations in Japanese siblings with CAGSSS, Leigh, and West syndrome
|
Takezawa, Yusuke
|
|
2018
|
40 |
10 |
p. 934-938
|
artikel
|
| 18 |
Quantitative evaluation of regional cerebral blood flow changes during childhood using 123I-N-isopropyl-iodoamphetamine single-photon emission computed tomography
|
Hirata, Yuko
|
|
2018
|
40 |
10 |
p. 841-849
|
artikel
|
| 19 |
Radiotherapy for Langerhans cell histiocytosis with paraplegia: A rare oncologic emergency case report in infancy and literature review
|
Nakashima, Kentaro
|
|
2018
|
40 |
10 |
p. 952-955
|
artikel
|
| 20 |
Rufinamide efficacy and safety in children aged 1–4 years with Lennox–Gastaut syndrome
|
Kim, Shin Hye
|
|
2018
|
40 |
10 |
p. 897-903
|
artikel
|
| 21 |
Two cases of childhood narcolepsy mimicking epileptic seizures in video-EEG/EMG
|
Yanagishita, Tomoe
|
|
2018
|
40 |
10 |
p. 939-942
|
artikel
|
| 22 |
Urinary prostaglandin metabolites as Duchenne muscular dystrophy progression markers
|
Takeshita, Eri
|
|
2018
|
40 |
10 |
p. 918-925
|
artikel
|
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