| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of abdominal functional myoclonus analyzed by movement related cortical potentials
|
Urabe, Ryosuke
|
|
|
42 |
9 |
p. 700-703
|
artikel
|
| 2 |
Additional observation of a de novo pathogenic variant in KCNT2 leading to epileptic encephalopathy with clinical features of frontal lobe epilepsy
|
Inuzuka, Luciana Midori
|
|
|
42 |
9 |
p. 691-695
|
artikel
|
| 3 |
Call for abstracts for Oral and Poster Presentations The 63rd Annual Meeting of the Japanese Society of Child Neurology JSCN 2021 “Ignite Evolution at the Dawn of a New Age”
|
|
|
|
42 |
9 |
p. I
|
artikel
|
| 4 |
Clinical spectrum of KIAA2022/NEXMIF pathogenic variants in males and females: Report of three patients from Indian kindred with a review of published patients
|
Panda, Prateek Kumar
|
|
|
42 |
9 |
p. 646-654
|
artikel
|
| 5 |
Contents
|
|
|
|
42 |
9 |
p. OBC
|
artikel
|
| 6 |
Cover
|
|
|
|
42 |
9 |
p. IBC
|
artikel
|
| 7 |
Editorial Board
|
|
|
|
42 |
9 |
p. IFC
|
artikel
|
| 8 |
Expanding the phenotype of COL4A1-related disorders—Four novel variants
|
Nishimura, Naoto
|
|
|
42 |
9 |
p. 639-645
|
artikel
|
| 9 |
Fifteen-year follow-up of a patient with a DHDDS variant with non-progressive early onset myoclonic tremor and rare generalized epilepsy
|
Togashi, Noriko
|
|
|
42 |
9 |
p. 696-699
|
artikel
|
| 10 |
Glucose transporter type 1 deficiency syndrome associated with autoantibodies to glutamate receptors
|
Hoshino, Hiroki
|
|
|
42 |
9 |
p. 686-690
|
artikel
|
| 11 |
IVIG in childhood primary angiitis of the central nervous system: A case report
|
Nishida, Hiroya
|
|
|
42 |
9 |
p. 675-679
|
artikel
|
| 12 |
Learning difficulties in Japanese schoolchildren with focal epilepsy
|
Miyazaki, Mitsuaki
|
|
|
42 |
9 |
p. 655-662
|
artikel
|
| 13 |
Longitudinal correspondence of epilepsy and scalp EEG fast (40–200 Hz) oscillations in pediatric patients with tuberous sclerosis complex
|
Tsuchiya, Hiroki
|
|
|
42 |
9 |
p. 663-674
|
artikel
|
| 14 |
Novel compound heterozygous ACO2 mutations in an infant with progressive encephalopathy: A newly identified neurometabolic syndrome
|
Park, Ji Soo
|
|
|
42 |
9 |
p. 680-685
|
artikel
|
| 15 |
Obituary
|
Casaer, Paul
|
|
|
42 |
9 |
p. 704
|
artikel
|
| 16 |
Sensory hypersensitivity in Tourette syndrome: A review
|
Isaacs, David
|
|
|
42 |
9 |
p. 627-638
|
artikel
|
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