| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A de novo CHD3 variant in a child with intellectual disability, autism, joint laxity, and dysmorphisms
|
Mizukami, Miyako
|
|
|
43 |
4 |
p. 563-565
|
artikel
|
| 2 |
Clinical manifestations and epilepsy treatment in Japanese patients with pathogenic CDKL5 variants
|
Kobayashi, Yu
|
|
|
43 |
4 |
p. 505-514
|
artikel
|
| 3 |
Contents
|
|
|
|
43 |
4 |
p. OBC
|
artikel
|
| 4 |
Cover
|
|
|
|
43 |
4 |
p. IBC
|
artikel
|
| 5 |
Early non-convulsive seizures are associated with the development of acute encephalopathy with biphasic seizures and late reduced diffusion
|
Maruyama, Azusa
|
|
|
43 |
4 |
p. 548-555
|
artikel
|
| 6 |
Early risk factors for encephalopathic transformation in children with benign childhood epilepsy with centrotemporal spikes
|
Porat Rein, Adi
|
|
|
43 |
4 |
p. 603-604
|
artikel
|
| 7 |
Early risk factors for encephalopathic transformation in children with benign childhood epilepsy with centrotemporal spikes
|
Panda, Prateek Kumar
|
|
|
43 |
4 |
p. 601-602
|
artikel
|
| 8 |
Editorial Board
|
|
|
|
43 |
4 |
p. IFC
|
artikel
|
| 9 |
Flurothyl-induced seizure paradigm revealed higher seizure susceptibility in middle-aged Angelman syndrome mouse model
|
Egawa, Kiyoshi
|
|
|
43 |
4 |
p. 515-520
|
artikel
|
| 10 |
GNAO1 mutation-related severe involuntary movements treated with gabapentin
|
Akasaka, Manami
|
|
|
43 |
4 |
p. 576-579
|
artikel
|
| 11 |
HPeV3-associated acute encephalitis/encephalopathy among Japanese infants
|
Abe, Yuichi
|
|
|
43 |
4 |
p. 528-537
|
artikel
|
| 12 |
Late-onset cerebral arteriopathy in a patient with incontinentia pigmenti
|
Kanai, Sotaro
|
|
|
43 |
4 |
p. 580-584
|
artikel
|
| 13 |
Malaysian outcome of acute necrotising encephalopathy of childhood
|
Fong, Choong Yi
|
|
|
43 |
4 |
p. 538-547
|
artikel
|
| 14 |
Neuroplasticity during the transition period: How the adolescent brain can recover from aphasia. A pilot study
|
Gárriz-Luis, Maite
|
|
|
43 |
4 |
p. 556-562
|
artikel
|
| 15 |
Peripheral nerves are involved in hypomyelinating leukodystrophy-3 caused by a homozygous AIMP1 variant
|
Hori, Ikumi
|
|
|
43 |
4 |
p. 590-595
|
artikel
|
| 16 |
Predictors of ADHD persistence in elementary school children who were assessed in earlier grades: A prospective cohort study from Istanbul, Turkey
|
Gökçe, Sebla
|
|
|
43 |
4 |
p. 495-504
|
artikel
|
| 17 |
Rapid-onset dystonia-parkinsonism with ATP1A3 mutation and left lower limb paroxysmal dystonia
|
Nomura, Shohei
|
|
|
43 |
4 |
p. 566-570
|
artikel
|
| 18 |
Refractory cerebral infarction in a child with an ACTA2 mutation
|
Kanamori, Keita
|
|
|
43 |
4 |
p. 585-589
|
artikel
|
| 19 |
Status dystonicus associated with CLN8 disease
|
Yıldırım, Miraç
|
|
|
43 |
4 |
p. 571-575
|
artikel
|
| 20 |
Thyroid crisis mimicking clinically mild encephalitis/encephalopathy with a reversible splenial lesion: A pediatric case report
|
Matsubara, Kohei
|
|
|
43 |
4 |
p. 596-600
|
artikel
|
| 21 |
Variance in the pathophysiological impact of the hemizygosity of gamma-aminobutyric acid type A receptor subunit genes between Prader-Willi syndrome and Angelman syndrome
|
Egawa, Kiyoshi
|
|
|
43 |
4 |
p. 521-527
|
artikel
|
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