| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A boy with a progressive neurologic decline harboring two coexisting mutations in KMT2D and VPS13D
|
Chang, Yu-Ming
|
|
|
45 |
10 |
p. 603-607
|
artikel
|
| 2 |
A female patient with adolescent-onset progressive myoclonus epilepsy carrying a truncating MECP2 mutation
|
Akiyama, Mari
|
|
|
45 |
10 |
p. 597-602
|
artikel
|
| 3 |
A screening method for visual attention disabilities in cerebral palsy with periventricular leukomalacia
|
Shimizu, Toshiyuki
|
|
|
45 |
10 |
p. 564-570
|
artikel
|
| 4 |
ATP6V1B2-related disorders featuring Lennox-Gastaut-syndrome: A case-based overview
|
Amore, Greta
|
|
|
45 |
10 |
p. 588-596
|
artikel
|
| 5 |
Contents
|
|
|
|
45 |
10 |
p. OBC
|
artikel
|
| 6 |
Cover
|
|
|
|
45 |
10 |
p. IBC
|
artikel
|
| 7 |
Editorial Board
|
|
|
|
45 |
10 |
p. IFC
|
artikel
|
| 8 |
Evaluation of the neurofilament light chain as a biomarker in children with spinal muscular atrophy treated with nusinersen
|
Seo, Gigyo
|
|
|
45 |
10 |
p. 554-563
|
artikel
|
| 9 |
Neurochemistry evaluated by magnetic resonance spectroscopy in a patient with FBXO28-related developmental and epileptic encephalopathy
|
Sano, Kentaro
|
|
|
45 |
10 |
p. 583-587
|
artikel
|
| 10 |
Pediatric anti-neutral glycosphingolipid antibodies-positive encephalomyeloradiculoneuropathy presenting with prominent brain demyelination
|
Ochiai, Satoru
|
|
|
45 |
10 |
p. 579-582
|
artikel
|
| 11 |
Progress in the treatment of neonatal hypoxic-ischemic encephalopathy with umbilical cord blood mononuclear cells
|
Zhou, Jiayu
|
|
|
45 |
10 |
p. 533-546
|
artikel
|
| 12 |
Severe and rare neurological manifestations following COVID-19 infection in children: A Malaysian tertiary centre experience
|
Anuar, Muhamad Azamin
|
|
|
45 |
10 |
p. 547-553
|
artikel
|
| 13 |
The gaze characteristics in preterm children: The appropriate timing for an eye-tracking tool
|
Yamase, Soichi
|
|
|
45 |
10 |
p. 571-578
|
artikel
|
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