| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Ambulatory capacity in Japanese patients with Duchenne muscular dystrophy
|
Awano, Hiroyuki
|
|
2018
|
40 |
6 |
p. 465-472
|
artikel
|
| 2 |
An infant case of diffuse cerebrospinal lesions and cardiomyopathy caused by a BOLA3 mutation
|
Nishioka, Makoto
|
|
2018
|
40 |
6 |
p. 484-488
|
artikel
|
| 3 |
Announcements and reports
|
|
|
2018
|
40 |
6 |
p. II-III
|
artikel
|
| 4 |
A novel mutation in sphingosine-1-phosphate lyase causing congenital brain malformation
|
Bamborschke, Daniel
|
|
2018
|
40 |
6 |
p. 480-483
|
artikel
|
| 5 |
A novel STXBP1 mutation causes typical Rett syndrome in a Japanese girl
|
Yuge, Kotaro
|
|
2018
|
40 |
6 |
p. 493-497
|
artikel
|
| 6 |
A novel truncating mutation in FLNA causes periventricular nodular heterotopia, Ehlers-Danlos-like collagenopathy and macrothrombocytopenia
|
Ieda, Daisuke
|
|
2018
|
40 |
6 |
p. 489-492
|
artikel
|
| 7 |
Anti-N-methyl-d-aspartate receptor encephalitis in children: Incidence and experience in Hong Kong
|
Ho, Alvin Chi-chung
|
|
2018
|
40 |
6 |
p. 473-479
|
artikel
|
| 8 |
Bickerstaff’s brainstem encephalitis with overlapping Guillain-Barré syndrome: Usefulness of sequential nerve conduction studies
|
Fong, Choong Yi
|
|
2018
|
40 |
6 |
p. 507-511
|
artikel
|
| 9 |
Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span
|
Yücel-Yılmaz, Didem
|
|
2018
|
40 |
6 |
p. 458-464
|
artikel
|
| 10 |
Contents
|
|
|
2018
|
40 |
6 |
p. OBC
|
artikel
|
| 11 |
Cover
|
|
|
2018
|
40 |
6 |
p. IBC
|
artikel
|
| 12 |
Development of a new screening tool for neuromotor development in children aged two – the neuromotor 5 min exam 2-year-old version (N5E2)
|
Aoki, Sayaka
|
|
2018
|
40 |
6 |
p. 445-451
|
artikel
|
| 13 |
Editorial Board
|
|
|
2018
|
40 |
6 |
p. IFC
|
artikel
|
| 14 |
Effect of botulinum toxin type A treatment in children with cerebral palsy: Sequential physical changes for 3 months after the injection
|
Matsuda, Mayumi
|
|
2018
|
40 |
6 |
p. 452-457
|
artikel
|
| 15 |
Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation
|
Miyauchi, Akihiko
|
|
2018
|
40 |
6 |
p. 498-502
|
artikel
|
| 16 |
Palliative non-resective surgery for drug-resistant epilepsy
|
Lattanzi, Simona
|
|
2018
|
40 |
6 |
p. 512-513
|
artikel
|
| 17 |
The hot cross bun sign in a patient with encephalitis
|
Gan, Yingyan
|
|
2018
|
40 |
6 |
p. 503-506
|
artikel
|
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