| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of CHOPS syndrome accompanied with moyamoya disease and systemic vasculopathy
|
Kim, Soo Yeon
|
|
|
43 |
3 |
p. 454-458
|
artikel
|
| 2 |
Acknowledgements to Anonymous Reviewers in 2020
|
|
|
|
43 |
3 |
p. I-III
|
artikel
|
| 3 |
A severe form of autosomal recessive spinocerebellar ataxia associated with novel PMPCA variants
|
Takahashi, Yoko
|
|
|
43 |
3 |
p. 464-469
|
artikel
|
| 4 |
Clinical evaluation of childhood cerebral adrenoleukodystrophy with balint’s symptoms
|
Kubota, Kazuo
|
|
|
43 |
3 |
p. 396-401
|
artikel
|
| 5 |
Clinical experience on the use of perampanel in epilepsy among child neurologists in the Philippines
|
Macrohon, Bernadette
|
|
|
43 |
3 |
p. 411-418
|
artikel
|
| 6 |
Congenital disorders of glycosylation type IIb with MOGS mutations cause early infantile epileptic encephalopathy, dysmorphic features, and hepatic dysfunction
|
Anzai, Rie
|
|
|
43 |
3 |
p. 402-410
|
artikel
|
| 7 |
Contents
|
|
|
|
43 |
3 |
p. OBC
|
artikel
|
| 8 |
Cover
|
|
|
|
43 |
3 |
p. IBC
|
artikel
|
| 9 |
Dravet syndrome with parkinsonian symptoms and intact dopaminergic neurons: A case report
|
Kanatani, Masahiro
|
|
|
43 |
3 |
p. 486-489
|
artikel
|
| 10 |
Editorial Board
|
|
|
|
43 |
3 |
p. IFC
|
artikel
|
| 11 |
Familial periodic paralysis associated with a rare KCNJ5 variant that supposed to have incomplete penetrance
|
Hiraide, Takuya
|
|
|
43 |
3 |
p. 470-474
|
artikel
|
| 12 |
Infection-associated decrease of serum creatine kinase levels in Fukuyama congenital muscular dystrophy
|
Takeshita, Saoko
|
|
|
43 |
3 |
p. 440-447
|
artikel
|
| 13 |
International classification of functioning, disability and health framework (ICF) based adaptive functioning outcomes of children with organic acidemias from a middle-income country
|
Akin, Ezgi Özalp
|
|
|
43 |
3 |
p. 389-395
|
artikel
|
| 14 |
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life
|
Battaglia, Domenica
|
|
|
43 |
3 |
p. 419-430
|
artikel
|
| 15 |
Neuroimaging manifestations and genetic heterogeneity of Walker-Warburg syndrome in Saudi patients
|
Alharbi, Sara
|
|
|
43 |
3 |
p. 380-388
|
artikel
|
| 16 |
Novel ACOX1 mutations in two siblings with peroxisomal acyl-CoA oxidase deficiency
|
Morita, Atsushi
|
|
|
43 |
3 |
p. 475-481
|
artikel
|
| 17 |
Novel de novo mutation substantiates ATP6V0C as a gene causing epilepsy with intellectual disability
|
Ittiwut, Chupong
|
|
|
43 |
3 |
p. 490-494
|
artikel
|
| 18 |
Pediatric headache: Are the red flags misleading or prognostic?
|
Yayıcı Köken, Özlem
|
|
|
43 |
3 |
p. 372-379
|
artikel
|
| 19 |
Polymicrogyria with calcification in Pallister-Killian syndrome detected by microarray analysis
|
Hiraiwa, Akiko
|
|
|
43 |
3 |
p. 448-453
|
artikel
|
| 20 |
Proteomic analysis reveals plasma haptoglobin, interferon-γ, and interleukin-1β as potential biomarkers of pediatric refractory epilepsy
|
Saengow, Vitchayaporn Emarach
|
|
|
43 |
3 |
p. 431-439
|
artikel
|
| 21 |
The eldest case of MICPCH with CASK mutation exhibiting gross motor regression
|
Nishio, Yosuke
|
|
|
43 |
3 |
p. 459-463
|
artikel
|
| 22 |
Transient hypoglycorrhachia with paroxysmal abnormal eye movement in early infancy
|
Tajima, Daisuke
|
|
|
43 |
3 |
p. 482-485
|
artikel
|
| 23 |
Transient structural MRI patterns correlate with the motor functions in preterm infants
|
Katušić, Ana
|
|
|
43 |
3 |
p. 363-371
|
artikel
|
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