| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A de novo p.Arg756Cys mutation in ATP1A3 causes a distinct phenotype with prolonged weakness and encephalopathy triggered by fever
|
Nakamura, Yuji
|
|
2018
|
40 |
3 |
p. 222-225
|
artikel
|
| 2 |
Announcements and reports
|
|
|
2018
|
40 |
3 |
p. I-III
|
artikel
|
| 3 |
A novel temporal pattern of childhood cerebral X-linked adrenoleukodystrophy
|
Turco, Emanuela C.
|
|
2018
|
40 |
3 |
p. 238-241
|
artikel
|
| 4 |
A quinidine non responsive novel KCNT1 mutation in an Indian infant with epilepsy of infancy with migrating focal seizures
|
Madaan, Priyanka
|
|
2018
|
40 |
3 |
p. 229-232
|
artikel
|
| 5 |
Brainstem infarction associated with HHV-6 infection in an infant
|
Wada, Aya
|
|
2018
|
40 |
3 |
p. 242-246
|
artikel
|
| 6 |
Contents
|
|
|
2018
|
40 |
3 |
p. OBC
|
artikel
|
| 7 |
Cover
|
|
|
2018
|
40 |
3 |
p. IBC
|
artikel
|
| 8 |
Determination of restless legs syndrome prevalence in children aged 13–16 years in the provincial center of Kayseri
|
Per, Hüseyin
|
|
2018
|
40 |
3 |
p. 256-257
|
artikel
|
| 9 |
Developmental trend of children with Down’s syndrome – How do sex and neonatal conditions influence their developmental patterns?
|
Aoki, Sayaka
|
|
2018
|
40 |
3 |
p. 181-187
|
artikel
|
| 10 |
Different MRI-defined tuber types in tuberous sclerosis complex: Quantitative evaluation and association with disease manifestations
|
Jesmanas, Simonas
|
|
2018
|
40 |
3 |
p. 196-204
|
artikel
|
| 11 |
Editorial Board
|
|
|
2018
|
40 |
3 |
p. IFC
|
artikel
|
| 12 |
Epileptic spasms secondary to acute cerebral and cerebellar encephalitis
|
Okanishi, Tohru
|
|
2018
|
40 |
3 |
p. 218-221
|
artikel
|
| 13 |
GRIN2A mutations in epilepsy-aphasia spectrum disorders
|
Yang, Xiaoling
|
|
2018
|
40 |
3 |
p. 205-210
|
artikel
|
| 14 |
Ketogenic diet using a Japanese ketogenic milk for patients with epilepsy: A multi-institutional study
|
Kumada, Tomohiro
|
|
2018
|
40 |
3 |
p. 188-195
|
artikel
|
| 15 |
Long-term follow up of an adult with alternating hemiplegia of childhood and a p.Gly755Ser mutation in the ATP1A3 gene
|
Ito, Tomoshiro
|
|
2018
|
40 |
3 |
p. 226-228
|
artikel
|
| 16 |
New quantitative method for evaluation of motor functions applicable to spinal muscular atrophy
|
Matsumaru, Naoki
|
|
2018
|
40 |
3 |
p. 172-180
|
artikel
|
| 17 |
Relationship between frequency spectrum of heart rate variability and autonomic nervous activities during sleep in newborns
|
Takatani, Tsunenori
|
|
2018
|
40 |
3 |
p. 165-171
|
artikel
|
| 18 |
The efficacy of adrenocorticotropic hormone in a girl with anti-N-methyl-D-aspartate receptor encephalitis
|
Hatanaka, Mari
|
|
2018
|
40 |
3 |
p. 247-250
|
artikel
|
| 19 |
Three children of meningoencephalitis with Kikuchi necrotizing lymphadenitis
|
Byun, Joung-Hee
|
|
2018
|
40 |
3 |
p. 251-255
|
artikel
|
| 20 |
TUBB3 E410K syndrome with osteoporosis and cough syncope in a patient previously diagnosed with atypical Moebius syndrome
|
Nakamura, Yasuko
|
|
2018
|
40 |
3 |
p. 233-237
|
artikel
|
| 21 |
Type I interferon and proinflammatory cytokine levels in cerebrospinal fluid of newborns with rotavirus-associated leukoencephalopathy
|
Lee, Kyung Yeon
|
|
2018
|
40 |
3 |
p. 211-217
|
artikel
|
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