nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A case of infantile Tay-Sachs disease with late onset spasms
|
Yamamoto, Naohiro |
|
|
43 |
5 |
p. 661-665 |
artikel |
2 |
Contents
|
|
|
|
43 |
5 |
p. OBC |
artikel |
3 |
Corrigendum to “Neurodevelopmental disorder associated with de novo SCN3A pathogenic variants: Two new cases and review of the literature” [Brain Dev. 42(2) (2020) 211–216]
|
Inuzuka, Luciana Midori |
|
|
43 |
5 |
p. 671 |
artikel |
4 |
Cover
|
|
|
|
43 |
5 |
p. IBC |
artikel |
5 |
Editorial Board
|
|
|
|
43 |
5 |
p. IFC |
artikel |
6 |
Electroencephalographic findings and genetic characterization of two brothers with IQSEC2 pathogenic variant
|
Izumi, Tatsuro |
|
|
43 |
5 |
p. 652-656 |
artikel |
7 |
Fine and gross motor skills predict later psychosocial maladaptation and academic achievement
|
Katagiri, Masatoshi |
|
|
43 |
5 |
p. 605-615 |
artikel |
8 |
Focal status and acute encephalopathy in a 13-year-old boy with de novo DNM1L mutation: Video-polygraphic pattern and clues for differential diagnosis
|
Mancardi, Maria Margherita |
|
|
43 |
5 |
p. 644-651 |
artikel |
9 |
Low-dose phenobarbital for epilepsy with myoclonic absences: A case report
|
Ito, Susumu |
|
|
43 |
5 |
p. 666-668 |
artikel |
10 |
Neurological complications after living-donor liver transplantation in children
|
Kanamori, Keita |
|
|
43 |
5 |
p. 637-643 |
artikel |
11 |
Parental germline mosaicism in SCN3A-related severe developmental disorder
|
Inuzuka, Luciana Midori |
|
|
43 |
5 |
p. 669-670 |
artikel |
12 |
Prediction of AESD and neurological sequelae in febrile status epilepticus
|
Nishiyama, Masahiro |
|
|
43 |
5 |
p. 616-625 |
artikel |
13 |
Prognostic factors for relapse and outcome in pediatric acute transverse myelitis
|
Helfferich, Jelte |
|
|
43 |
5 |
p. 626-636 |
artikel |
14 |
Unexpected elevation in valproic acid concentration and agranulocytosis in a patient with short-chain acyl-CoA dehydrogenase deficiency
|
Suzuki, Yuki |
|
|
43 |
5 |
p. 657-660 |
artikel |