| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Activation of leukocyte immunoglobulin-like receptor B2 signaling pathway in cortical lesions of pediatric patients with focal cortical dysplasia type IIb and tuberous sclerosis complex
|
Yue, Jiong
|
|
2019
|
41 |
10 |
p. 829-838
|
artikel
|
| 2 |
Announcements and Reports
|
|
|
2019
|
41 |
10 |
p. I-II
|
artikel
|
| 3 |
A 16q22.2-q23.1 deletion identified in a male infant with West syndrome
|
Mori, Tatsuo
|
|
2019
|
41 |
10 |
p. 888-893
|
artikel
|
| 4 |
ARX-associated infantile epileptic-dyskinetic encephalopathy with responsiveness to valproate for controlling seizures and reduced activity of muscle mitochondrial complex IV
|
Kwong, Anna Ka-Yee
|
|
2019
|
41 |
10 |
p. 883-887
|
artikel
|
| 5 |
A severe case of Menkes disease with repeated bone fracture during the neonatal period, followed by multiple arterial occlusion
|
Kobayashi, Satoru
|
|
2019
|
41 |
10 |
p. 878-882
|
artikel
|
| 6 |
Automatic calculation of Mercuri grades from CT and MR muscle images
|
Nakayama, Takahiro
|
|
2019
|
41 |
10 |
p. 870-877
|
artikel
|
| 7 |
Breastfeeding and risk of febrile seizures in infants: The Japan Environment and Children’s Study
|
Mitsuda, Naomi
|
|
2019
|
41 |
10 |
p. 839-847
|
artikel
|
| 8 |
Contents
|
|
|
2019
|
41 |
10 |
p. OBC
|
artikel
|
| 9 |
Cover
|
|
|
2019
|
41 |
10 |
p. IBC
|
artikel
|
| 10 |
Developmental outcomes and prevalence of SLC2A1 variants in young infants with hypoglycorrhachia
|
Yu, Wen-Hao
|
|
2019
|
41 |
10 |
p. 854-861
|
artikel
|
| 11 |
Editorial Board
|
|
|
2019
|
41 |
10 |
p. IFC
|
artikel
|
| 12 |
Fulminant cerebral venous thrombosis associated with the m.3243A>G MELAS mutation: A new guise for an old disease
|
Nikolaus, Marc
|
|
2019
|
41 |
10 |
p. 901-904
|
artikel
|
| 13 |
High incidence of status epilepticus and ongoing seizures on arrival to the hospital due to high prevalence of febrile seizures in Izumo, Japan: A questionnaire-based study
|
Kimura, Masahiko
|
|
2019
|
41 |
10 |
p. 848-853
|
artikel
|
| 14 |
Neuropsychological outcomes of childhood acute necrotizing encephalopathy
|
Williams, Tracey A.
|
|
2019
|
41 |
10 |
p. 894-900
|
artikel
|
| 15 |
Single-fiber electromyography-based diagnosis of CACNA1A mutation in children: A potential role of the electrodiagnosis in the era of whole exome sequencing
|
Hirasawa-Inoue, Ayaka
|
|
2019
|
41 |
10 |
p. 905-909
|
artikel
|
| 16 |
Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy
|
Shibata, Akiko
|
|
2019
|
41 |
10 |
p. 862-869
|
artikel
|
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