| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Announcements and reports and Call for Papers
|
|
|
2019
|
41 |
9 |
p. I
|
artikel
|
| 2 |
Association of inattention with slow-spindle density in sleep EEG of children with attention deficit-hyperactivity disorder
|
Saito, Yoshihiko
|
|
2019
|
41 |
9 |
p. 751-759
|
artikel
|
| 3 |
Central nervous system vasculitis from Epstein-Barr virus-associated T/natural killer-cell lymphoproliferative disorder in children: A case report
|
Lee, Mi Seon
|
|
2019
|
41 |
9 |
p. 820-825
|
artikel
|
| 4 |
Contents
|
|
|
2019
|
41 |
9 |
p. OBC
|
artikel
|
| 5 |
Cover
|
|
|
2019
|
41 |
9 |
p. IBC
|
artikel
|
| 6 |
Cumulative jerk as an outcome measure in nonambulatory Duchenne muscular dystrophy
|
Fujii, Tatsuya
|
|
2019
|
41 |
9 |
p. 796-802
|
artikel
|
| 7 |
Editorial Board
|
|
|
2019
|
41 |
9 |
p. IFC
|
artikel
|
| 8 |
Fetal growth restriction: From Polyvagal theory to developmental impairments?
|
Aldrete-Cortez, Vania
|
|
2019
|
41 |
9 |
p. 769-775
|
artikel
|
| 9 |
Gender differences in occurrence of behavioral and emotional problems at the lower grades of elementary school: Association with developmental and behavioral characteristics at 5 years
|
Zen, Yui
|
|
2019
|
41 |
9 |
p. 760-768
|
artikel
|
| 10 |
Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders
|
Yamamoto, Toshiyuki
|
|
2019
|
41 |
9 |
p. 776-782
|
artikel
|
| 11 |
Letter to the editor
|
Gadoth, Natan
|
|
2019
|
41 |
9 |
p. 826
|
artikel
|
| 12 |
Long-term outcome of a group of Japanese children with myelin-oligodendrocyte glycoprotein encephalomyelitis without preventive immunosuppressive therapy
|
Hino-Fukuyo, Naomi
|
|
2019
|
41 |
9 |
p. 790-795
|
artikel
|
| 13 |
Novel RASA1 mutations in Japanese pedigrees with capillary malformation-arteriovenous malformation
|
Moteki, Yosuke
|
|
2019
|
41 |
9 |
p. 812-816
|
artikel
|
| 14 |
Perampanel attenuates myoclonus in a patient with neuronal ceroid lipofuscinoses type 2 disease
|
Wong, Lee Chin
|
|
2019
|
41 |
9 |
p. 817-819
|
artikel
|
| 15 |
Phenotypic manifestations between male and female children with CDKL5 mutations
|
Liang, Jao-Shwann
|
|
2019
|
41 |
9 |
p. 783-789
|
artikel
|
| 16 |
Prediction of poor neurological development in patients with symptomatic congenital cytomegalovirus diseases after oral valganciclovir treatment
|
Fukushima, Sachiyo
|
|
2019
|
41 |
9 |
p. 743-750
|
artikel
|
| 17 |
Reply to the comments on “Spontaneous spinal epidural hematoma mimicking Guillain-Barre Syndrome”
|
Yamaguchi, Hiroshi
|
|
2019
|
41 |
9 |
p. 827-828
|
artikel
|
| 18 |
Transition from Leigh syndrome to MELAS syndrome in a patient with heteroplasmic MT-ND3 m.10158T>C
|
Kori, Atsuko
|
|
2019
|
41 |
9 |
p. 803-807
|
artikel
|
| 19 |
Usefulness of diagnostic tools in a GLUT1 deficiency syndrome patient with 2 inherited mutations
|
Dozières-Puyravel, Blandine
|
|
2019
|
41 |
9 |
p. 808-811
|
artikel
|
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